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Article

In Vitro Anticancer Activity of Methanolic Extract of Justicia adhatoda Leaves with Special Emphasis on Human Breast Cancer Cell Line

by
Sonu Kumar
1,†,
Rajveer Singh
2,†,
Debrupa Dutta
1,
Shivani Chandel
2,
Arka Bhattacharya
2,
Velayutham Ravichandiran
2,* and
Soumi Sukla
1,*
1
Department of Pharmacology & Toxicology, National Institute of Pharmaceutical Education and Research, 168, Maniktala Main Road, Kolkata 700054, India
2
Department of Natural Products, National Institute of Pharmaceutical Education and Research, 168, Maniktala Main Road, Kolkata 700054, India
*
Authors to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Molecules 2022, 27(23), 8222; https://doi.org/10.3390/molecules27238222
Submission received: 19 September 2022 / Revised: 14 October 2022 / Accepted: 25 October 2022 / Published: 25 November 2022
(This article belongs to the Special Issue Natural and Synthetic Anti-cancer Drug Discovery)
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Abstract

:
Natural products are being targeted as alternative anticancer agents due to their non-toxic and safe nature. The present study was conducted to explore the in vitro anticancer potential of Justicia adhatoda (J. adhatoda) leaf extract. The methanolic leaf extract was prepared, and the phytochemicals and antioxidant potential were determined by LCMS analysis and DPPH radical scavenging assay, respectively. A docking study performed with five major alkaloidal phytoconstituents showed that they had a good binding affinity towards the active site of NF-κB. Cell viability assay was carried out in five different cell lines, and the extract exhibited the highest cytotoxicity in MCF-7, a breast cancer cell line. Extract-treated cells showed a significant increase in nitric oxide and reactive oxygen species production. Cell cycle analysis showed an arrest in cell growth at the Sub-G0 phase. The extract successfully inhibited cell migration and colony formation and altered mitochondrial membrane potential. The activities of superoxide dismutase and glutathione were also found to decrease in a dose-dependent manner. The percentage of apoptotic cells was found to increase in a dose-dependent manner in MCF-7 cells. The expressions of caspase-3, Bax, and cleaved-PARP were increased in extract-treated cells. An increase in the expression of NF-κB was found in the cytoplasm in extract-treated cells. J. adhatoda leaf extract showed a potential anticancer effect in MCF-7 cells.

1. Introduction

Noncommunicable diseases (NCDs) such as cancer are widely acknowledged as a global health problem that lacks a universal solution [1]. Breast cancer (BC) is the primary cause of premature death in women among the various types of cancer. In the United States, breast cancer accounts for the second most cancer deaths in women after lung cancer. BC can be triggered by a range of risk factors such as race, ethnicity, family history of cancer, genetic features, and modifiable exposures such as alcohol consumption, physical inactivity, exogenous hormones, and certain female reproductive variables [2]. Breast cancer, when detected at early stages, is treatable, particularly when it is still limited to the breast areas or has only migrated to the axillary lymph nodes. Advancements in multimodal therapy have increased the chances of a cure in 70–80% of patients. The advanced (metastatic) stage of breast cancer, on the other hand, is considered to be untreatable with the present therapeutic options [3]. Despite significant advancements in cancer treatment tactics, adverse effects and resistance to currently available anticancer medications are among the leading causes of treatment failure in 80% of patients [4]. Chemotherapeutic agents are highly effective in treating breast cancer, but they must be used for an extended period to obtain optimum results. Currently, targeted breast cancer therapy includes tamoxifen, fulvestrant, herceptin, and aromatase inhibitors. However, chemotherapeutic drug resistance is the major hurdle to overcome [5]. In addition to curing cancer, it can induce adverse health conditions such as ovarian and endometrial hyperplasia and carcinomas, as well as multiple vein thrombosis and pulmonary embolism [6]. Chemotherapeutic agents attack malignant cells and eradicate them, but they can also harm healthy cells and tissues, resulting in a significant decrease in patient life expectancy. As a result, innovative, target-oriented, safe, and low-cost therapeutic strategies are needed. Medicinal plants are relatively safe and inexpensive. Therefore, they could be a good alternative for potential new anticancer compounds [7]. Natural products and phytomedicines are the biggest hope for curing various human degenerative diseases, including cancer. Plants have been investigated as a source of medicinally relevant bioactive components, and many of them, such as Taxol, Camptothecin, Vincristine, Vinblastine, Vinorelbine, Vindesine, Vinflunine, and others, appear to have a strong therapeutic value in the treatment of a variety of malignancies [8]. Several plant species, including Taxus brevifolia Nutt, Curcuma longa, Podophyllum peltatum, and Catharanthus roseus, have been demonstrated to have potent anticancer properties against various types of cancer including breast cancer [9,10].
J. adhatoda (Acanthaceae), commonly known as Vasaka or Malabar, is an important medicinal plant used in ayurvedic and different traditional medicine systems [11]. It is distributed throughout the South Asia and Indo-China region and is natively found in India, Afghanistan, Bangladesh, East Himalayas, Laos, Myanmar, Nepal, Pakistan, Sri Lanka, and Vietnam [12,13]. It was also introduced into China, Cuba, Ethiopia, Jamaica, Madagascar, and Sicilia [12,13]. Various components of the plant are used to cure asthma, joint pain, lumber pain, sprains, colds, coughs, eczema, malaria, rheumatism, swelling, and venereal infections [11,14]. Plant leaves have anti-inflammatory properties and are also used as cardiotonic, expectorant, and anti-asthma agents [15]. Various leaf mixtures are often used in Southeast Asia to treat bleeding, skin illnesses, wounds, headaches, snake bites, and leprosy [16,17]. J. adhatoda has been studied for its antioxidant, hepatoprotective, anti-inflammatory, antibacterial, antiprotozoal, hypolipidemic, antiasthmatic, and abortifacient properties [18]. Alkaloids, tannins, saponins, phenolics, and flavonoids are bioactive phytochemicals found in the leaves of J. adhatoda. Pyrroquinazoline alkaloids such as vasicine, vasicol, vasicinone, and peganine, as well as other minor elements, make up the majority of it [19,20].
In light of these observations, the current study has been taken up to evaluate the anticancer properties of J. adhatoda leaf extract with particular emphasis on MCF-7, a breast cancer cell line.

2. Results

2.1. Phytochemical Composition of Methanolic Extract of J. adhatoda

LC/MS analysis of the methanolic extract of J. adhatoda leaves showed 81 compounds belonging to different chemical classes (Table S1 and Figure S1).

2.2. DPPH Radical Scavenging Assay

The DPPH assay is used to predict antioxidant activities by mechanism in which antioxidants inhibit oxidation and therefore determine free radical scavenging activity. The method is based on the scavenging of DPPH radicals by antioxidants, which, upon a reduction reaction, decolorize the purple DPPH solution [21]. The extract showed mild antioxidant potential with a significant increase in free radical scavenging activity in a concentration-dependent manner, and 30% free radical inhibition was observed at 250 µg/mL of extract, the highest concentration studied (Figure 1).

2.3. Docking Study

The plant’s active alkaloidal constituents include vasicine, l-vasicinone, deoxyvasicine, maiontone, vasicinolone, and vasicinol, among others, which have been extensively explored for a variety of pharmacological uses. Previously these molecules were explored for various antibacterial [22] and anti-neurodegenerative disorders [23] in in silico models. Therefore, these phytoconstituents were chosen for the molecular docking investigation [24,25,26]. NF-κB is a well-known transcription factor for biological responses, immune regulation, and inflammation, but mounting evidence indicates it also participates in oncogenesis and promotes the growth and spread of breast cancer. NF-κB activity is seen in many lymphoid or myeloid tumors, including multiple myeloma, Hodgkin diseases, and some non-Hodgkin lymphomas [27]. This transcription factor can, in most cases, protect transformed cells from apoptosis and thus participate in the onset or progression of many human cancers. Additionally, many solid tumors, including breast malignancies, glioblastomas, and many others, have NF-κB overexpression that makes them resistant to chemotherapeutic drugs such as tamoxifen and paclitaxel [28,29]. Hence, NF-κB is thought to be a target for drugs that fight breast cancer, and the molecular docking study with five major alkaloidal phytoconstituents of the extract showed significant binding affinity towards the active site NF-κB and can act as NF-κB inhibitor (Figure 2). The binding energy of the individual compounds is given in Table 1.

2.4. Evaluation of the Cytotoxicity of J. adhatoda Leaf Extract on Different Cell Lines

The anticancer activity of J. adhatoda leaf extract was evaluated by MTT assay on different cell lines, namely HEK-293, RAW 264.7, SHSY-5Y, MCF-7, and A549 after 24 h of treatment with different concentrations of J. adhatoda leaf extract (50 µg/mL, 100 µg/mL, 150 µg/mL, 200 µg/mL and 250 µg/mL) (Figure S2). The extract has shown significant decline in % cell viability with an IC50 value of 257.44 µg/mL in RAW264.7, 364.57 µg/mL in SHSY-5Y, 161.57 µg/mL in MCF-7 and 170.12 µg/mL in A549 (Figure 3A). The IC50 value for HEK-293 was found to be much higher, i.e., 695.86 µg/mL, suggesting that the extract is less cytotoxic on non-cancerous cell lines. According to our findings, the extract has shown the most cytotoxic effect on the MCF-7 cell line (Figure 3A). Standard drug paclitaxel showed concentration-dependent cytotoxicity in MCF-7 cells post 24 h treatment (Figure 3B).

2.5. J. adhatoda Leaf Extract Induces NO Production in MCF-7 Cell Line

Nitric oxide (NO) is an important cell signaling molecule. NO has a dual role in cancer biology; at concentrations of more than 500 nM, nitrogen species were found to possess a cytotoxic effect [30]. NO species induces cell death by causing DNA damage. The result showed a significant increase in NO production in MCF-7 cells treated with J. adhatoda leaf extract and standard drug paclitaxel as compared to control cells (Figure 4).

2.6. J. adhatoda Leaf Extract Induces ROS Production in MCF-7 Cell Line

In cellular physiopathology, ROS play a crucial role in cell proliferation, signaling pathways, and oxidative defense systems that kill microorganisms and cancerous cells. For this reason, the measurement of intracellular ROS production could represent a very useful parameter to quantify oxidative stress and its significance as an anticancer agent. Intracellular ROS quantification using fluorescent DCFDA dye showed that MCF-7 cells treated with J. adhatoda leaf extract resulted in more ROS production in a concentration-dependent manner than control cells with extract concentration of 150 µg/mL and 0.1 µM paclitaxel exhibiting similar ROS production (Figure 5A).

2.7. Effect of J. adhatoda Leaf Extract on Mitochondrial Membrane Potential (ΔΨM)

Mitochondria are involved in cell apoptosis, and the mitochondrial membrane potential (ΔΨM) is an important parameter to determine the mitochondrial function that can be utilized as an indicator of cell health. The integrity of the mitochondrial membrane was investigated in MCF-7 cells using JC-1 stain after treatment with J. adhatoda leaf extract. JC-1 accumulates and oligomerizes in the mitochondrial matrix of healthy cells, leading to the production of red fluorescence. Whereas in unhealthy cells having reduced mitochondrial membrane potential, JC-1 appears as a monomer and emits green fluorescence. The red/green fluorescence ratio is a measurement of mitochondrial membrane potential. The results obtained from confocal microscopy imaging showed a decreased red/green fluorescence intensity in J. adhatoda treated MCF-7 cells compared to control cells, indicating J. adhatoda induces mitochondrial membrane depolarization (Figure 5B,C).

2.8. Effect of J. adhatoda Leaf Extract on Glutathione (GSH) and Glutathione Disulfide (GSSG) Level

Malignant cells have a high metabolic activity, which results in the formation of a lot of free radicals. Under oxidative stress, GSH reduces to form GSSG. The ratio of GSH/GSSG is inversely proportional to the level of oxidative stress. GSH in cancerous cells elevates to maintain the balance of oxidative stress. The result obtained by treating MCF-7 cells with J. adhatoda leaf extract depicts that the extract reduces intracellular GSH levels (Figure 5D), which further results in the generation of ROS and induction of apoptosis in MCF-7 cells.

2.9. Effect of J. adhatoda Leaf Extract on Superoxide Dismutase Activity

Superoxide dismutase plays a crucial role in scavenging free radicals within cells, but oxidative radicals also significantly eliminate pathogens and cancerous cells. A plot of % SOD activity with an increase in J. adhatoda leaf extract concentrations at different time points (0, 10, 20, 30, 40, 50, and 60 min) revealed that J. adhatoda leaf extracts lowered % SOD activity in a concentration-dependent manner (Figure 5E).

2.10. J. adhatoda Leaf Extract Induces Apoptosis

Apoptosis is a standard physiologic procedure of controlled cell death to maintain stable homeostasis. Annexin V-FITC and propidium iodide (PI) double staining method showed that cells treated with J. adhatoda leaf extract (100 μg/mL and 150 μg/mL) induced early and late apoptosis compared to control cells (Figure 6A). These findings indicate that J. adhatoda induces apoptosis in a concentration-dependent manner in MCF-7 cells.

2.11. J. adhatoda Leaf Extract Induces Sub-G0 and S-Phase Cell Cycle Arrest

Cell cycle arrest is one of the most important methods by which anticancer drugs inhibit tumor progression. Generally, the G0/G phase is characterized by 2n (diploid), the G2/M phase by 4n (tetraploid), and the S phase between 2n and 4n. The impact of J. adhatoda leaf extract treatment on cell cycle phase propagation of the MCF-7 cells was evaluated. The results showed normal distribution of the G1, S, and G2/M phase in control cells. In contrast, cells treated with J. adhatoda leaf extract showed significant cell arrest at the Sub-G0 phase of the cell cycle (Figure 6B).

2.12. Effect of J. adhatoda Leaf Extract on Apoptosis-Related Protein Expression

Caspase-3, Bax, and cleaved-PARP are the major apoptosis-related protein molecules; hence measuring their expression in cells provides crucial data on apoptosis. The expression of these proteins in MCF-7 cells treated with J. adhatoda leaf extract was determined by Western blot analysis (Figure 6C). The results demonstrate that the expression of apoptotic proteins (Bax, caspase-3, and cleaved-PARP) was elevated compared to the control (Figure 6D).

2.13. Evaluation of J. adhatoda Leaf Extract on Colony Formation of MCF-7 Cells

Cancer cells grow in colonies in conjunction with adjacent cells; losing contact with adjoining cells leads to their death. The results obtained from the clonogenic assay (Figure 7A) showed a decrease in colony formation in J. adhatoda leaf extract-treated MCF-7 cells compared to that of control cells. The colonial/population density of each plate was measured and plotted (Figure 7B). The results showed that the colony growth was decreased by approximately 50% and 80% in cells treated with 100 μg/mL and 150 μg/mL of J. adhatoda leaf extract, respectively, compared to control cells. The result supports the anticancer role of J. adhatoda leaf extract.

2.14. J. adhatoda Leaf Extract Showed Inhibitory Activity in Cell Migration

MCF-7 control cells exhibited wound-healing properties and cell migration, and the gap was almost closed. On the contrary, significant inhibition of wound healing or cell migration was observed in the MCF-7 cells treated with J. adhatoda leaf extract (at concentrations of 100 μg/mL and 150 μg/mL) (Figure 7C). Percentage wound closure significantly declined in a concentration-dependent manner (Figure 7D). These results suggest that J. adhatoda leaf extract possesses anticancer properties.

2.15. Evaluation of J. adhatoda Leaf Extract on NF-κB Translocation

NF-κB is a well-known transcription factor in biological responses, immunological control, and inflammation, but accumulating evidence suggests it also plays a role in oncogenesis. Immunostaining of J. adhatoda leaf extract-treated MCF-7 cells using an anti-NF-κB antibody indicate that NF-κB translocated from cytoplasm to nucleus in control cells, but after treatment with J.adhatoda leaf extract at concentrations 100 μg/mL and 150 μg/mL, NF-κB expression was increased in the cytoplasm (Figure 8).

3. Discussion

Breast cancer is one of the most common cancers in women and is the leading cause of female death globally. BC is characterized by tumor heterogeneity, which leads to drug resistance to chemotherapy [3]. In developed countries, advances in diagnostic techniques and awareness of mammographic screening have significantly lowered the number of BC cases, but this is still an issue in developing countries [31]. It is curable if detected early or at the non-metastatic stage; however, it is incurable if detected later or after the spread of the metastasis using the currently available chemotherapeutic agents [4]. Treatment of BC is becoming increasingly difficult due to major side effects associated with existing therapies such as chemotherapy and radiotherapy. Currently, multidrug resistance to chemotherapy has made it difficult to treat BC patients, resulting in an increase in the number of cases as well as a decrease in patient survival rates [32]. To tackle this life-threatening illness, numerous research projects are currently committed to discovering alternative BC therapy systems that can be employed as therapies or adjuvant treatments alongside chemotherapeutic agents [33]. Natural compounds have attracted the scientific community’s attention in the hunt for more effective and less toxic medications for the treatment of cancer, particularly breast cancer, and have opened up a new area in chemotherapeutic research [34]. Curcumin derived from turmeric, resveratrol derived from grapes, and quercetin derived from citrus fruits have been demonstrated to have anticancer effects in pancreatic and colorectal cancer [35]. Many natural compounds extracted from herbs, such as paclitaxel [36], vincristine [37], cantharidin sodium injection [38], and Magnolol [39], have been demonstrated in clinical studies to have strong anti-breast cancer activity [40]. In this study, we explored the antiproliferative activity and mechanism of action of J. adhatoda leaf extract in the MCF-7 breast cancer cell line. J. adhatoda leaf extract did not show any significant antioxidant activity and was effective in killing tumor cells (RAW 264.7, SHSY-5Y, A549, and MCF-7) while showing a minimal effect on non-cancerous cells (HEK-293). Among all the tested cell lines, J. adhatoda has shown significant toxicity against the breast cancer cell line (MCF-7). Therefore, the breast cancer cell line MCF-7 was chosen to test further anticancer properties of the extract. The clonogenic assay showed that J. adhatoda leaf extract promoted breast cancer cell death and inhibited colony formation in an anchorage-independent manner. Cell migration is a key phase in the development and metastasis of cancer, and cancer metastasis is linked to the stimulation of cancer cell migration and invasion of the nearby tissues making it important to study and understand in order to combat the disease [41,42]. Furthermore, as demonstrated by a wound-healing assay, the extract inhibited cell migration and proliferation. The production of ROS and reactive nitrogen species (RNS) is required for cancer cells to grow, proliferate, and spread. Due to the higher metabolic rate, malignant cells produce more ROS and RNS. Depending on their local concentration, these species play pleiotropic functions in cancer and can cause tumor development or tumor suppression [43]. Simultaneously, excess ROS and RNS production over the required amount may cause oxidative stress in cancer cells, leading to death and a reduction in chemotherapy resistance [44,45]. In order to check the activity of the extract against ROS and RNS production, ROS assay by DCFDA method and NO assay by Griess reagent were performed. The results obtained from these assays suggest that J. adhatoda leaf extract produced both ROS and RNS in considerable amounts and in a concentration-dependent manner in the MCF-7 cell line and that paclitaxel treatment also did the same [46]. The extract’s anticancer properties are probably related to the presence of phytochemicals disrupting the MCF-7 cells’ redox balance, which is necessary for survival. After exposure to J. adhatoda leaf extract, higher percentages of apoptosis and cell cycle arrest at Sub-G0 and S-phase have been detected in a concentration-dependent manner. Apoptosis was further confirmed by Western blot analysis of apoptotic markers (Caspase-3, Bax, and cleaved-PARP). NF-κB is a vital transcription factor that links inflammation to cancer, and previous data suggest that NF-κB has a role in breast cancer tumorigenesis and chemotherapeutic resistance [47]. The expression of NF-κB p65 declined in the nucleus of MCF-7 cells after treatment with typical chemotherapeutic medicines (Tamoxifen) in breast cancer cells [48]. The current study also showed that the extract dramatically reduced NF-κB expression in the nucleus of MCF-7 cells in a concentration-dependent manner compared to the control group. Docking studies confirmed that the major alkaloidal phytoconstituents of the extracts, such as vasicine, vasicinol, vasicinone, deoxyvasicinone, and vasicinolone, have a significant binding affinity towards the active site of NF-κB and can act as NF-κB inhibitors. From the above findings, it can be stated that J. adhatoda leaf extract has anti-breast cancer potential because it can induce apoptosis by activating apoptotic proteins (caspase-3, Bax, and cleaved-PARP), prevent cells from entering in Sub-G0 phase of the cell cycle and inactivate the NF-κB pathway. Overall, our findings suggest that J. adhatoda would be an effective treatment for chemotherapeutic-resistant breast cancer. Further pre-clinical studies on J. adhatoda leaf extract in animal models of breast cancer are warranted to check its chemotherapeutic potential.

4. Materials and Methods

4.1. Preparation of Mathanolic Extract of J. Adhatoda Leaves

J. adhatoda plants were collected from the West Bengal State Medicinal Plants Board, Kolkata, washed thoroughly, and shade dried at room temperature. The dried leaves were ground with a mechanical grinder to make a coarse powder and were sieved (mesh size #40) to separate large particles [12]. Further, 100 g of dried powder was macerated in 500 mL of methanol for 15 days with continuous shaking, followed by filtration with Whattman No. 1 filter paper. The filtrate was concentrated using a rotary evaporator (Heidolph Instruments GmbH & CO. KG, Schwabach, Germany). The concentrated extract was vacuum dried and stored at 4 °C [49].

4.2. Analysis of Plant Extract by LC-MS

Chromatographic separation (Agilent Technologies 1290 Infinity ıı, Agilent Technologies, Waldbronn, Germany) was achieved on an ACQUITY UPLC®HSS C18 column (2.1 × 100 mm, 1.8 μm). The mobile phase consisted of acetonitrile as solvent A, methanol as solvent B, and 0.5% acetic acid in water as solvent C (Table S2). The flow rate was 0.6 mL/min, and the column temperature was set at 20 °C. The diode-array detection was set to monitor at 270 nm. The mass spectrometry analysis was performed using a 6545 Q-TOF LC/MS coupled mass spectrometer, with the following conditions: source temperature: 350 °C; ion spray voltage −4.5 kV; Gas 1, Gas 2, curtain gas, and collision gas (nitrogen) were separately set at 50, 50, 45, and 12 psi; sheath gas flow rate, 40 arbitrary units; auxiliary gas flow rate, 5 arbitrary units; electrospray voltage, 3.5 kV; capillary voltage, −32 V; capillary temperature, 270 °C [50].

4.3. DPPH Free Radical Scavenging Activity

To assess the antioxidant potential of J. adhatoda leaf extract, DPPH radical scavenging assay was conducted according to Naqvi et al. with few modifications [51,52]. Briefly, 24 mg of 2,2-diphenyl-1-picrylhydrazyl (DPPH) reagent was dissolved in 100 mL methanol, and the absorbance was checked to be 1.08–1.1 at 517 nm. Then, 100 µL of extract in concentrations of 50 µg/mL, 100 µg/mL, 150 µg/mL, 200 µg/mL, and 250 µg/mL was added to 100 µL DPPH solution and incubated for 20 min at room temperature in dark. The absorbance was checked at 517 nm. % inhibition of free radicals was calculated using the following formula:
%inhibition = [(absorbancecontrol − absorbancesample)/absorbancecontrol] × 100

4.4. Molecular Docking of the J. adhatoda Leaf Extract towards NF-κB

The list of phytochemicals present in J. adhatoda was prepared from the LC-QTOF-MS data. A total of 81 compounds were identified, and from them, 5 most active compounds were selected for docking study. The three-dimensional (3D) conformers of these compounds were downloaded from the PubChem database in SDF format. Similarly, the 3D structure of protein NF-κB (PDB ID: 1LE5) was acquired from the protein data bank (https://www.rcsb.org/, (accessed on 15 June 2022)). The 3D structures of the ligands were optimized with LigPrep (Schrödinger Release 2022-2: LigPrep, Schrödinger, LLC, New York, NY, USA, 2021), and receptor structure was optimized and prepared for docking using Protein Preparation Wizard. The active site of the proteins was evaluated by SiteMap, and the grid was generated through the Receptor Grid generator. Further, the optimized ligand and the receptor were docked using Ligand Docking in Glide-V9.2. The probable poses were observed through Pose Viewer. The Docking analysis was performed in Schrödinger Release 2022-2: Maestro, Schrödinger, LLC, New York, NY, USA, 2021.

4.5. Cell Culture

RAW 264.7 cells (murine macrophage cell line), HEK-293 cells (Human embryonic kidney cell line), SHSY-5Y cells (neuroblastoma cell line), MCF-7 cells (Michigan Cancer Foundation-7 cell line), and A549 cells (adenocarcinomic human alveolar basal epithelial cell line) were obtained from NCCS, Pune, India and maintained in Dulbecco’s modified Eagle’s medium (DMEM) supplemented with 10% (v/v) fetal bovine serum (FBS) and penicillin-streptomycin (1% v/v) (Gibco, Grand Island, NY, USA). The cells were grown in a humidified incubator at 37 °C with 5% carbon dioxide [53].

4.6. Measurement of Cell Viability

HEK-293 cells, RAW 264.7 cells, SHSY-5Y cells, MCF-7 cells, and A549 cells were seeded in a 96-well plate (1 × 104 cells/well) containing DMEM media supplemented with 10% FBS and incubated for 24 h. Cells were treated with different concentrations of J. adhatoda leaf extract (50 µg/mL, 100 µg/mL, 150 µg/mL, 200 µg/mL and 250 µg/mL) and paclitaxel (Sigma) with 0.01 µM, 0.1 µM, and 1 µM concentrations are used as positive control and incubated at 37 °C with 5% CO2 for 24 h. Further, 10 µL of MTT (3-(4, 5-dimethyl thiazolyl-2)-2, 5-diphenyltetrazolium bromide) reagent (5 mg/mL in 1X phosphate buffer saline) was added to each well, and cells were incubated for 4 h at 37 °C in 5% CO2. Subsequently, cells were washed with 1X PBS, and the insoluble formazan crystals were solubilized with 200 μL of dimethyl sulphoxide (DMSO). Absorbance was measured by using a microplate reader (Synergy H1 microplate reader, Biotek, Santa Clara, CA, USA) at 570 nm [54].
% viable cells = (OD of sample − OD of blank)/(OD of control − OD of blank) × 100

4.7. Nitric Oxide (NO) Production Assay

For quantification of NO production, MCF-7 cells were seeded in 6 well plates (3 × 105 cells/well) and incubated for 12 h at 37 °C in a 5% CO2 incubator [55]. The media from each well was removed, and the cells were treated with 2 mL J. adhatoda leaf extract in serum-free media at concentrations of 100 µg/mL and 150 µg/mL, and 0.1 µM of paclitaxel treatment was used as standard positive control. After 1 h of treatment, the presence of nitrite was determined by taking the cell supernatant using a commercial NO detection kit (Sigma-Aldrich, St. Louis, MO, USA). Briefly, 50 μL of cell supernatant with an equal volume of Griess reagent was incubated in a 96-well plate at room temperature for 30 min [50]. Absorbance was measured by a microplate reader (Synergy H1 microplate reader, Biotek, Santa Clara, CA, USA) at 540 nm. The amount of nitrite in the media was calculated from the sodium nitrite (NaNO2) standard curve [56,57].

4.8. Measurement of Intracellular ROS Generation by DCFDA

For the quantification of intracellular reactive oxygen species (ROS) production, MCF-7 cells were seeded in 12-well plates (1 × 105 cells/well) and incubated for 24 h [58]. The cells were then treated with 100 µg/mL and 150 µg/mL concentrations of J. adhatoda leaf extract, and 0.1 µM of paclitaxel treatment was used as standard positive control for 24 h. After 24 h of treatment, cells were incubated with 10 μM DCFDA for 30 min at 37 °C in the dark. Further, cells were detached using 0.25% trypsin-ethylenediaminetetraacetic acid (EDTA), centrifuged at 500× g for 5 min, and resuspended in 1X PBS. The flow cytometric analysis was performed using BD LSRFortessaTM Cell Analyzer (Becton, Dickinson and Company, San Jose, CA, USA) [59], and data were analyzed using FACS analysis software (FlowJoTM v 10.8 BD bioscience, San Jose, CA, USA).

4.9. Measurement of Mitochondrial Membrane Potential (ΔΨM) by JC-1

For mitochondrial membrane potential analysis, MCF-7 cells were plated in a confocal plate (1 × 104 cells/well) and incubated overnight. The 80–90% confluent cells were treated with 100 µg/mL and 150 µg/mL concentration of J. adhatoda leaf extract for 24 h. After 24 h of treatment, the cells were washed with 1X PBS, and cells were re-incubated in fresh culture media with 2 µL of JC-1 dye (5 mg/mL) for 30 min at 37 °C. Media was removed, and the cells were washed 3 times with warm 1X PBS. Then, 1 mL of 1X PBS was added to each plate and covered with a sheet of aluminum foil. The fluorescence of the test culture was captured by using a confocal microscope (STELLARIS5, Leica Biosystems, Wetzlar, Germany) with 100X magnification [60].

4.10. Quantitative Determination of Glutathione (GSH) and Glutathione Disulfide (GSSG)

For quantification of the reduced sulfhydryl form (GSH) and the oxidized glutathione disulfide form (GSSG), MCF-7 cells were seeded in a 6-well plate (3 × 105 cells/well) and incubated for 24 h. Next, cells were treated with 100 µg/mL and 150 µg/mL of J. adhatoda leaf extract for 24 h. After 24 h of treatment, cells were washed twice with 1X PBS and trypsinized using trypsin–EDTA for 5 min at room temperature (22–25 °C) [61,62]. Quantification of GSH and GSSG from cell lysate was performed using DetectX Glutathione (GSH) Fluorescent Detection kit (ArborAssaysTM, Ann Arbor, MI, USA) following the manufacturer’s instructions, and fluorescence was measured by a microplate reader (Synergy H1 microplate reader, Biotek, Santa Clara, CA, USA) at 510 nm emission and 370–410 nm excitation wavelength, respectively.

4.11. Determination of the Superoxide Dismutase Activity

Superoxide dismutase (SOD) activity of J. adhatoda leaf extract (50 µg/mL, 100 µg/mL, 150 µg/mL, 200 µg/mL, and 250 µg/mL) was determined by SOD Determination Kit (Sigma-Aldrich, Catalogue no. 19160) following manufacturer’s instructions. The absorbance was measured using a microplate reader (Synergy H1 microplate reader, Biotek) at 450 nm to assess the SOD mimetic activity of J. adhatoda leaf extract in an aqueous solution at 25 °C. A plot of percentage SOD inhibition vs. J. adhatoda leaf extract concentration (µg/mL) at different time points was used to establish the IC50 value for WST (water-soluble tetrazolium salt) inhibition [63].

4.12. Quantification of Apoptotic Cells by Annexin V-PI

Apoptotic cell quantification was performed by annexin V-FITC and propidium iodide (PI) double staining method. MCF-7 cells were seeded into 12-well plates (1 × 105 cells/well) and incubated for 24 h. Cells were treated with 100 µg/mL and 150 µg/mL of J. adhatoda leaf extract for 24 h. Next, the cells were washed twice with ice-cold 1X PBS and centrifuged at 500× g for 5 min at 4 °C. The cells were subjected to annexin V and PI staining, and the samples were run in a flow cytometer using BD LSRFortessaTM Cell Analyzer. Apoptotic cells were quantified by using FACS analysis software (FlowJoTM v 10.8 BD bioscience, San Jose, CA, USA).

4.13. Cell Cycle Analysis

Cell cycle analysis is essential in identifying the precise mechanism of cell arrest in a specific phase of the cell cycle [64]. For cell cycle analysis, MCF-7 cells were seeded in 12-well plates (1 × 105 cells/well) and incubated at 37 °C with 5% CO2 for 24 h. The cells were treated with 100 µg/mL and 150 µg/mL concentrations of J. adhatoda leaf extract for 24 h. After 24 h, cells were centrifuged at 500× g for 5 min. The supernatant was discarded, and the pellet was redissolved in 70% ethanol. The cells were incubated at 4 °C overnight [65]. After incubation, the cells were centrifuged, and the cell pellet was washed twice with 1X PBS. Next, cells were resuspended in 100 μL of 1X PBS. RNAse was added, and the cells were incubated at 37 °C for 4 h. The centrifugation and washing steps were repeated. The cells were resuspended in 100 μL of 1X PBS, and 5 μL (5 mg/mL) of propidium iodide (PI) was added, and samples were incubated for 30 min at room temperature. The samples were run in a flow cytometer by using BD LSRFortessaTM Cell Analyzer, and data were analyzed using FACS analysis software (FlowJoTM v 10.8 BD bioscience, San Jose, CA, USA) [66].

4.14. Western Blot Analysis

MCF-7 cells were cultured for 24 h and treated with 100 µg/mL and 150 µg/mL concentrations of J. adhatoda leaf extract. Total protein from each sample was extracted using a radioimmunoprecipitation assay (RIPA Lysis and Extraction Buffer #89900) lysis solution, including phosphatase inhibitors. Using a Pierce™ BCA Protein Assay kit (Pierce™ BCA Protein Assay Kit #23225), the protein concentration was determined [67]. For each sample, an equivalent amount of protein was mixed with loading buffer to form an equal volume, and then the sample was denatured at 95 °C for 15 min. Further, the protein was separated on a 10% SDS-PAGE gel and transferred to the PVDF membrane [68]. The membranes were blocked for 2 h with blocking buffer (5% skim milk in 1X PBS buffer with 0.1% Tween 20), followed by incubation at 4 °C overnight with primary antibodies against β-actin (1:1000, Rabbit, Cell signaling #5174S), Bax (1:1000, Rabbit pAb, ABclonal #A19684), Caspase-3 (1:1000, Rabbit pAb, ABclonal #A2156) and cleaved-PARP (poly ADP-ribose polymerase, 1:1000, Rabbit, Cell signaling #9542). Next, the membranes were washed with 1X PBST buffer twice at 5 min intervals. Further, the membranes were incubated with horseradish peroxidase (HRP)-conjugated secondary antibody (Goat Anti-Rabbit, 1:4000, ABclonal #AS014) for 1 hr. The protein expression levels were determined using enhanced chemiluminescence (ECL) with ChemiDoc TM XRS+ (Biorad).

4.15. Clonogenic Assay

For the clonogenic assay, MCF-7 cells were seeded in 12-well plates. On reaching 80–90% confluency, cells were treated with 100 µg/mL and 150 µg/mL of J. adhatoda leaf extract for 24 h. After 24 h, the cells were trypsinized and seeded at a density of 5 × 103 cells per well in a 12-well plate, followed by incubation for 14 days. Further, the cells were rinsed with 1X PBS and fixed in a 3.7% formaldehyde solution for 30 min. The fixed cells were then stained with bromophenol and incubated for another 30 min. The plates were washed with 1X PBS and allowed to dry at room temperature. Images were captured, and colonies were counted manually [69].

4.16. Wound Healing/Scratch Assay/Cell Migration Assay

For wound healing (scratch) assay, MCF-7 cells were seeded in a 12-well plate and were allowed to reach confluency up to 80–90%. A uniform scratch was made on the monolayer in each well using a 2.5 μL sterile pipette tip. The cells were rinsed with sterile 1X PBS to remove debris before being treated with 100 µg/mL and 150 µg/mL J. adhatoda leaf extract for 24 h and 48 h. The images of the cells were acquired with the help of an inverted microscope (Nikon-SC600) with 10× magnification to record the data, and the % wound closure was measured using ImageJ (Software 1.53 s, Wayne Rasband, National Institutes of Health, Bethesda, MD, USA). The percentage of wound closure area was determined as
% wound closure = [(Area of wound at 0 h − Area of wound at 24 h and 48 h)/Area of wound at 0 h] × 100
The experiment was repeated in triplicate.

4.17. Translocation of NF-κB

For nuclear factor κB (NF-κB) translocation analysis, cells were plated in a confocal plate (1 × 104 cells/well). After 24 h, the cells were treated with 100 µg/mL and 150 µg/mL of J. adhatoda leaf extract for 24 h. Next, the cells were washed with 1X PBS and fixed with 4% formaldehyde in 1X PBS for 15 min. The fixed cells were permeabilized with 0.5% Triton-X100 in 1X PBS for 15 min, followed by blocking with 3% BSA for 1 h. Further, the cells were incubated with anti-NF-κB p65 (Cell signaling #3033) primary monoclonal antibody overnight at 4 °C. The cells were then washed with 1X PBS and further incubated with a secondary antibody conjugated with Alexa Fluor 488 (1:500, Anti-Rabbit; Cell signaling #4412S) for another 1 h. Samples were washed with 1X PBS. Cells were stained with DAPI for 1 h at 37 °C, and images were acquired using a confocal microscope (STELLARIS5, Leica Biosystems, Wetzlar, Germany) with 100× magnification [70,71].

5. Conclusions

The current study was undertaken to check the potential of J. adhatoda leaf extract as an anticancer agent. In silico studies with the five major alkaloid phytoconstituents of the extract indicated significant binding affinity towards the active site of NF-κB and potential as an NF-κB inhibitor. The extract increased NO and ROS production, whereas superoxide dismutase and glutathione activities were decreased when MCF-7, a breast cancer cell line, was treated with it. The extract inhibited cell migration and colony formation and altered mitochondrial membrane potential. The extract showed anti-breast cancer potential, as it induces apoptosis by activating apoptotic proteins like caspase-3, Bax, and cleaved-PARP. The extract also prevented cells from entering in Sub-G0 phase of the cell cycle. All of these in vitro studies clearly indicated the anti-breast cancer potential of the extract. When compared with Paclitaxel, one of the currently available drugs to treat breast cancer, the extract showed similar results. Natural products, when used for treatments, show minimal adverse effects. Currently available breast cancer chemotherapeutics sometimes fail to provide desired results and show different side effects as well as resistance to chemotherapy. To overcome these problems, anticancer agents from natural sources are being investigated worldwide. It can be concluded from the findings of the current study that J. adhatoda leaf extract has a high potential as an alternative therapy for breast cancer. Further pre-clinical studies need to be conducted to develop it as an anti-breast cancer agent.

Supplementary Materials

The following are available online at https://www.mdpi.com/article/10.3390/molecules27238222/s1, Figure S1: LCMS Justicia adhatoda leaf extract. The chromatogram was obtained by Q-TOF-LCMS analysis of Justicia adhatoda leaf extract to determine its phytoconstituents, Figure S2: MTT assay of J. adhatoda leaf extract in different cell lines, Table S1: List of phytochemicals obtained by LC-MS analysis of J. adhatoda methanolic extract, Table S2: The gradient of the mobile phase for chromatographic separation.

Author Contributions

Conceptualization, R.S., S.K. and S.S.; Methodology, R.S. and S.K.; Software, A.B.; Validation, R.S., Formal Analysis, R.S., A.B. and S.S.; Resources, S.C. and V.R.; Writing—Original Draft Preparation, S.K.; Writing—Review and Editing, D.D. and S.S.; Visualization, R.S. and S.S.; Supervision, S.S. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The datasets used and analyzed during the study are available from the corresponding author upon reasonable request.

Acknowledgments

The authors wish to thank NIPER-Kolkata for providing infrastructural support and funding. The authors thank Soma Das for her help in acquiring the LC-MS data.

Conflicts of Interest

The authors declare that there is no conflict of interest to report.

Sample Availability

Samples of the compounds are available from the corresponding authors.

References

  1. Global Burden of Disease Cancer Collaboration; Fitzmaurice, C.; Abate, D.; Abbasi, N.; Abbastabar, H.; Abd-Allah, F.; Abdel-Rahman, O.; Abdelalim, A.; Abdoli, A.; Abdollahpour, I.; et al. Global, regional, and national cancer incidence, mortality, years of life lost, years lived with disability, and disability-adjusted life-years for 29 cancer groups, 1990 to 2017: A systematic analysis for the global burden of disease study. JAMA Oncol. 2019, 5, 1749–1768. [Google Scholar] [PubMed] [Green Version]
  2. Coughlin, S.S. Epidemiology of breast cancer in women. Adv. Exp. Med. Biol. 2019, 1152, 9–29. [Google Scholar] [PubMed]
  3. Harbeck, N.; Penault-Llorca, F.; Cortes, J.; Gnant, M.; Houssami, N.; Poortmans, P.; Ruddy, K.; Tsang, J.; Cardoso, F. Breast cancer. Nat. Rev. Dis. Prim. 2019, 5, 66. [Google Scholar] [CrossRef] [PubMed]
  4. Khamis, A.A.A.; Ali, E.M.M.; El-Moneim, M.A.A.; Abd-Alhaseeb, M.M.; El-Magd, M.A.; Salim, E.I. Hesperidin, piperine and bee venom synergistically potentiate the anticancer effect of tamoxifen against breast cancer cells. Biomed. Pharmacother. 2018, 105, 1335–1343. [Google Scholar] [CrossRef] [PubMed]
  5. Lukong, K.E. Understanding breast cancer–The long and winding road. BBA Clin. 2017, 7, 64–77. [Google Scholar] [CrossRef] [PubMed]
  6. Davies, C.; Pan, H.; Godwin, J.; Gray, R.; Arriagada, R.; Raina, V.; Abraham, M.; Medeiros Alencar, V.H.; Badran, A.; Bonfill, X.; et al. Long-term effects of continuing adjuvant tamoxifen to 10 years versus stopping at 5 years after diagnosis of oestrogen receptor-positive breast cancer: ATLAS, a randomised trial. Lancet 2013, 381, 805–816. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  7. Bournine, L.; Bensalem, S.; Fatmi, S.; Bedjou, F.; Mathieu, V.; Iguer-Ouada, M.; Kiss, R.; Duez, P. Evaluation of the cytotoxic and cytostatic activities of alkaloid extracts from different parts of Peganum harmala L. (Zygophyllaceae). Eur. J. Integr. Med. 2017, 9, 91–96. [Google Scholar] [CrossRef]
  8. Greenwell, M.; Rahman, P. Medicinal Plants: Their Use in Anticancer Treatment. Int. J. Pharm. Sci. Res. 2015, 6, 4103–4112. [Google Scholar]
  9. Fridlender, M.; Kapulnik, Y.; Koltai, H. Plant derived substances with anti-cancer activity: From folklore to practice. Front. Plant Sci. 2015, 6, 799. [Google Scholar] [CrossRef]
  10. Alam, S.; Katiyar, D.; Goel, R.; Vats, A.; Mittal, A. Role of herbals in cancer management. J. Phytopharm. 2013, 2, 46–51. [Google Scholar] [CrossRef]
  11. Jain, S.K. Dictionary of Indian Folk Medicine and Ethnobotany; Deep Publications: New Delhi, India, 1991. [Google Scholar]
  12. Chowdhury, I.I.; Rahman, A.; Hashem, M.A.; Bhuiyan, M.M.H.; Hajjar, D.; Alelwani, W.; Makki, A.A.; Haque, A.; Tangpong, J.; Bin Bakhtiar, M.T. Supplements of an aqueous combination of Justicia adhatoda and Ocimum tenuiflorum boost antioxidative effects and impede hyperlipidemia. Anim. Model. Exp. Med. 2020, 3, 140–151. [Google Scholar] [CrossRef] [PubMed]
  13. Bobkov, V.; van der Woning, B.; de Haard, H. Display Technologies for Generation of Ig Single Variable Domains; Methods in Molecuar Biology Series; Humana Press: New York, NY, USA, 2018; Volume 1827, pp. 129–144. [Google Scholar]
  14. Eep, D.; Ramanjeet, K.; Seema, D. A review on Justicia adhatoda: A potential source of natural medicine. Afr. J. Plant Sci. 2013, 5, 620–627. [Google Scholar]
  15. Khan, A.M.; Bhadauria, S. Isolation of Some Potential Phytocompounds from Adhatoda Vasica through Gas Chromatography-Mass Spectroscopy Analysis. Asian J. Pharm. Clin. Res. 2017, 10, 328–332. [Google Scholar] [CrossRef] [Green Version]
  16. Rastogi, R.P.; Mehrotra, B. Compendium of Indian Medicinal Plants; Central Drug Research Institute: Uttar Pradesh, India, 1990. [Google Scholar]
  17. Chopra, N.R.; Chopra, I.C. Indigenous Drugs of India; Academic Publishers: Kolkata, India, 1994. [Google Scholar]
  18. Gutti, U.; Komati, J.K.; Kotipalli, A.; Saladi, R.G.V.; Gutti, R.K. Justicia adhatoda induces megakaryocyte differentiation through mitochondrial ROS generation. Phytomedicine 2018, 43, 135–139. [Google Scholar] [CrossRef] [PubMed]
  19. Khan, R.; Shamsi, Y.; Nikhat, S. Medicinal benefits of Adhatoda vasica Nees.-in unani and contemporary medicine. Cellmed 2020, 10, 13.1–13.7. [Google Scholar]
  20. Khan, R.; Shamsi, Y.; Nikhat, S. Modulatory influence of Adhatoda vesica (Justicia adhatoda) leaf extract on the enzymes of xenobiotic metabolism, antioxidant status and lipid peroxidation in mice. Mol. Cell Biochem. 2000, 213, 99–109. [Google Scholar]
  21. Badmanaban, R.; Prajapati Milan, G.; Patel, C.N.; Sen, D.J.; Bibhuranjan, P. Studies on leaf extracts of drug Punarnava by comparing its antioxidant potential by spectrophotometric method. Res. J. Pharm. Technol. 2010, 3, 566–569. [Google Scholar]
  22. Gatadi, S.; Lakshmi, T.V.; Nanduri, S. 4(3H)-Quinazolinone derivatives: Promising antibacterial drug leads. Eur. J. Med. Chem. 2019, 170, 157–172. [Google Scholar] [CrossRef]
  23. Du, H.; Jiang, X.; Ma, M.; Xu, H.; Liu, S.; Ma, F. Novel deoxyvasicinone and tetrahydro-beta-carboline hybrids as inhibitors of acetylcholinesterase and amyloid beta aggregation. Bioorganic Med. Chem. Lett. 2020, 30, 127659. [Google Scholar] [CrossRef]
  24. Shoaib, A.J.C. A systematic ethnobotanical review of Adhatoda vasica (L.), Nees. Cell. Mol. Biol. 2021, 67, 248–263. [Google Scholar] [CrossRef] [PubMed]
  25. Avula, B.; Begum, S.; Ahmed, S.; Choudhary, M.I.; Khan, I.A. Quantitative determination of vasicine and vasicinone in Adhatoda vasica by high performance capillary electrophoresis. Pharm.-Int. J. Pharm. Sci. 2008, 63, 20–22. [Google Scholar]
  26. Suryanarayana, A.A.; Shankar, S.; Manoharan, J.P.; Subramanian, V. In-Silico analysis and molecular docking studies of phytoconstituents of Justicia adhatoda as potential inhibitors of SARS-CoV2 target proteins. In Proceedings of the First International Conference on Combinatorial and Optimization, ICCAP 2021, Chennai, India, 7–8 December 2021. [Google Scholar]
  27. Ranganatha, S.; Shruthi, S.D.; Govindappa, M.; Ramachandra, Y.L. In silico studies of NF-κB protein as anti-cancer and anti-inflammatory target. J. Comput. Methods Mol. 2013, 3, 26–33. [Google Scholar]
  28. Esparza-López, J.; Longoria, O.; La Cruz-Escobar, D.; Neftali, E.; Garibay-Díaz, J.C.; León-Rodríguez, E.; Ibarra-Sánchez MD, J. Paclitaxel resistance is mediated by NF-κB on mesenchymal primary breast cancer cells. Oncol. Lett. 2022, 23, 50. [Google Scholar] [CrossRef] [PubMed]
  29. Kastrati, I.; Joosten, S.E.P.; Semina, S.E.; Alejo, L.H.; Brovkovych, S.D.; Stender, J.D.; Horlings, H.M.; Kok, M.; Alarid, E.T.; Greene, G.L.; et al. The NF-κB Pathway Promotes Tamoxifen Tolerance and Disease Recurrence in Estrogen Receptor–Positive Breast Cancers. Mol. Cancer Res. 2020, 18, 1018–1027. [Google Scholar] [CrossRef] [Green Version]
  30. Vannini, F.; Kashfi, K.; Nath, N. The dual role of iNOS in cancer. Redox Biol. 2015, 6, 334–343. [Google Scholar] [CrossRef] [Green Version]
  31. Britt, K.L.; Cuzick, J.; Phillips, K.-A. Key steps for effective breast cancer prevention. Nat. Cancer 2020, 20, 417–436. [Google Scholar] [CrossRef]
  32. Doyle, L.A.; Yang, W.; Abruzzo, L.V.; Krogmann, T.; Gao, Y.; Rishi, A.K.; Ross, D.D. A multidrug resistance transporter from human MCF-7 breast cancer cells. Proc. Natl. Acad. Sci. USA 1998, 95, 15665–15670. [Google Scholar] [CrossRef] [PubMed]
  33. Mitra, S.; Dash, R. Natural Products for the Management and Prevention of Breast Cancer. Evidence-Based Complement. Altern. Med. 2018, 2018, 8324696. [Google Scholar] [CrossRef]
  34. Preet, R.; Mohapatra, P.; Mohanty, S.; Sahu, S.K.; Choudhuri, T.; Wyatt, M.D.; Kundu, C.N. Quinacrine has anticancer activity in breast cancer cells through inhibition of topoisomerase activity. Int. J. Cancer 2012, 130, 1660–1670. [Google Scholar] [CrossRef]
  35. Jani, T.S.; DeVecchio, J.; Mazumdar, T.; Agyeman, A.; Houghton, J.A. Inhibition of NF-κB signaling by quinacrine is cytotoxic to human colon carcinoma cell lines and is synergistic in combination with tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) or oxaliplatin. J. Biol. Chem. 2010, 285, 19162–19172. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  36. Bourgeois-Daigneault, M.-C.; St-Germain, L.E.; Roy, D.G.; Pelin, A.; Aitken, A.S.; Arulanandam, R.; Falls, T.; Garcia, V.; Diallo, J.-S.; Bell, J.C. Combination of Paclitaxel and MG1 oncolytic virus as a successful strategy for breast cancer treatment. Breast Cancer Res. 2016, 18, 83. [Google Scholar] [CrossRef] [Green Version]
  37. Zeng, F.; Ju, R.-J.; Liu, L.; Xie, H.-J.; Mu, L.-M.; Lu, W.-L. Efficacy in Treating Lung Metastasis of Invasive Breast Cancer with Functional Vincristine Plus Dasatinib Liposomes. Pharmacology 2018, 101, 43–53. [Google Scholar] [CrossRef]
  38. Wang, L.; Huang, X.-E.; Cao, J. Clinical Study on Safety of Cantharidin Sodium and Shenmai Injection Combined with Chemotherapy in Treating Patients with Breast Cancer Postoperatively. Asian Pac. J. Cancer Prev. 2014, 15, 5597–5600. [Google Scholar] [CrossRef] [Green Version]
  39. Ranaware, A.M.; Banik, K.; Deshpande, V.; Padmavathi, G.; Roy, N.K.; Sethi, G.; Fan, L.; Kumar, A.P.; Kunnumakkara, A.B. Magnolol: A Neolignan from the Magnolia Family for the Prevention and Treatment of Cancer. Int. J. Mol. Sci. 2018, 19, 2362. [Google Scholar] [CrossRef] [Green Version]
  40. Wang, X.; Yang, Y.; An, Y.; Fang, G. The mechanism of anticancer action and potential clinical use of kaempferol in the treatment of breast cancer. Biomed. Pharmacother. 2019, 117, 109086. [Google Scholar] [CrossRef] [PubMed]
  41. Pijuan, J.; Barceló, C.; Moreno, D.F.; Maiques, O.; Sisó, P.; Marti, R.M.; Macià, A.; Panosa, A. In vitro Cell Migration, Invasion, and Adhesion Assays: From Cell Imaging to Data Analysis. Front. Cell Dev. Biol. 2019, 7, 107. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  42. Clemente, N.; Argenziano, M.; Gigliotti, C.L.; Ferrara, B.; Boggio, E.; Chiocchetti, A.; Caldera, F.; Trotta, F.; Benetti, E.; Annaratone, L.; et al. Paclitaxel-Loaded Nanosponges Inhibit Growth and Angiogenesis in Melanoma Cell Models. Front. Pharmacol. 2019, 10, 776. [Google Scholar] [CrossRef]
  43. Mishra, D.; Patel, V.; Banerjee, D. Nitric Oxide and S-Nitrosylation in Cancers: Emphasis on Breast Cancer. Breast Cancer Basic Clin. Res. 2020, 14. [Google Scholar] [CrossRef]
  44. Qian, Q.; Chen, W.; Cao, Y.; Cao, Q.; Cui, Y.; Li, Y.; Wu, J. Targeting Reactive Oxygen Species in Cancer via Chinese Herbal Medicine. Oxidative Med. Cell. Longev. 2019, 2019, 9240426. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  45. Salaroglio, I.C.; Gazzano, E.; Abdullrahman, A.; Mungo, E.; Castella, B.; Abd-Ellatef, G.E.; Massaia, M.; Donadelli, M.; Rubinstein, M.; Riganti, C.; et al. Increasing intratumor C/EBP-β LIP and nitric oxide levels overcome resistance to doxorubicin in triple negative breast cancer. J. Exp. Clin. Cancer Res. 2018, 37, 286. [Google Scholar] [CrossRef] [Green Version]
  46. Ren, X.; Zhao, B.; Chang, H.; Xiao, M.; Wu, Y.; Liu, Y. Paclitaxel suppresses proliferation and induces apoptosis through regulation of ROS and the AKT/MAPK signaling pathway in canine mammary gland tumor cells. Mol. Med. Rep. 2018, 17, 8289–8299. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  47. Khongthong, P.; Roseweir, A.K.; Edwards, J. The NF-KB pathway and endocrine therapy resistance in breast cancer. Endocr.-Relat. Cancer 2019, 26, R369–R380. [Google Scholar] [CrossRef] [PubMed]
  48. Nehra, R.; Riggins, R.B.; Shajahan, A.N.; Zwart, A.; Crawford, A.C.; Clarke, R. BCL2 and CASP8 regulation by NF-κB differentially affect mitochondrial function and cell fate in antiestrogen-sensitive and-resistant breast cancer cells. FASEB J. 2010, 24, 2040–2055. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  49. Sudevan, S.; Parasivam, R.; Sundar, S.; Velauthan, H.; Ramasamy, V. Investigation of anti-inflammatory and anti-cancer activity of Justicia adathoda metabolites. Pak. J. Pharm. Sci. 2019, 32, 1555–1561. [Google Scholar]
  50. Yan, N.; Wen, D.S.; Zhao, Y.R.; Xu, S.J. Epimedium sagittatum inhibits TLR4/MD-2 mediated NF-κB signaling pathway with anti-inflammatory activity. BMC Complement. Altern. Med. 2018, 18, 303. [Google Scholar] [CrossRef] [Green Version]
  51. Naqvi, S.A.R.; Waseem, R.; Mahmood, N.; Hussain, Z.; Khan, Z.A.; Shahzad, S.A.; Yar, M.; Amin, R.; Bukhari, S.A.; Zahoor, A.F.; et al. Phenolic acid content, antioxidant properties, and antibacterial potential of flowers and fruits from selected Pakistani indigenous medicinal plants. ScienceAsia 2013, 39, 340–345. [Google Scholar] [CrossRef] [Green Version]
  52. Naqvi, S.A.R.; Ali, S.; Sherazi, T.A.; Haq, A.-U.; Saeed, M.; Sulman, M.; Rizwan, M.; Alkahtani, S.; Abdel-Daim, M.M. Antioxidant, antibacterial, and anticancer activities of bitter gourd fruit extracts at three different cultivation stages. J. Chem. 2020, 2020, 7394751. [Google Scholar] [CrossRef]
  53. Michael, S.; Montag, M.; Dott, W. Pro-inflammatory effects and oxidative stress in lung macrophages and epithelial cells induced by ambient particulate matter. Environ. Pollut. 2013, 183, 19–29. [Google Scholar] [CrossRef] [PubMed]
  54. Huang, C.-Y.; Sivalingam, K.; Shibu, M.A.; Liao, P.-H.; Ho, T.-J.; Kuo, W.-W.; Chen, R.-J.; Day, C.-H.; Viswanadha, V.P.; Ju, D.-T. Induction of Autophagy by Vasicinone Protects Neural Cells from Mitochondrial Dysfunction and Attenuates Paraquat-Mediated Parkinson’s Disease Associated α-Synuclein Levels. Nutrients 2020, 12, 1707. [Google Scholar] [CrossRef]
  55. Wu, J.; Chen, Y.; Bai, L.; Liu, Y.; Fu, X.; Zhu, P.; Li, J.; Chou, J.; Yin, C.; Wang, Y.; et al. Chrysoeriol ameliorates TPA-induced acute skin inflammation in mice and inhibits NF-κB and STAT3 pathways. Phytomedicine 2020, 68, 153173. [Google Scholar] [CrossRef]
  56. Fan, H.; Gao, Z.; Ji, K.; Li, X.; Wu, J.; Liu, Y.; Wang, X.; Liang, H.; Liu, Y.; Li, X.; et al. The in vitro and in vivo anti-inflammatory effect of osthole, the major natural coumarin from Cnidium monnieri (L.) Cuss, via the blocking of the activation of the NF-κB and MAPK/p38 pathways. Phytomedicine 2019, 58, 152864. [Google Scholar] [CrossRef]
  57. Gasparrini, M.; Forbes-Hernandez, T.Y.; Giampieri, F.; Afrin, S.; Alvarez-Suarez, J.M.; Mazzoni, L.; Mezzetti, B.; Quiles, J.L.; Battino, M. Anti-inflammatory effect of strawberry extract against LPS-induced stress in RAW 264.7 macrophages. Food Chem. Toxicol. 2017, 102, 1–10. [Google Scholar] [CrossRef]
  58. Zou, Y.; Wang, A.; Shi, M.; Chen, X.; Liu, R.; Li, T.; Zhang, C.; Zhang, Z.; Zhu, L.; Ju, Z.; et al. Analysis of redox landscapes and dynamics in living cells and in vivo using genetically encoded fluorescent sensors. Nat. Protoc. 2018, 13, 2362–2386. [Google Scholar] [CrossRef] [PubMed]
  59. Oh, B.; Lee, C.H. Development of Thiolated-Graphene Quantum Dots for Regulation of ROS in macrophages. Pharm Res. 2016, 33, 2736–2747. [Google Scholar] [CrossRef] [PubMed]
  60. Sivandzade, F.; Bhalerao, A.; Cucullo, L. Analysis of the Mitochondrial Membrane Potential Using the Cationic JC-1 Dyeas a Sensitive Fluorescent Probe. Bio-Protoc. 2019, 9, e3128. [Google Scholar] [CrossRef] [PubMed]
  61. Rahman, I.; Kode, A.; Biswas, S.K. Assay for quantitative determination of glutathione and glutathione disulfide levels using enzymatic recycling method. Nat. Protoc. 2006, 1, 3159–3165. [Google Scholar] [CrossRef]
  62. Li, C.; Zhang, S.; Li, L.; Hu, Q.; Ji, S. Ursodeoxycholic Acid Protects Against Arsenic Induced Hepatotoxicity by the Nrf2 Signaling Pathway. Front. Pharmacol. 2020, 11, 594496. [Google Scholar] [CrossRef]
  63. Al–Asbahy, W.M.; Shamsi, M. Dynamics, Synthesis and characterization of Copper–based anticancer compound; in vitro interaction studies with DNA/HSA, SOD mimetic, cytotoxic activity and molecular docking investigation. J. Biomol. Struct. Dyn. 2021, 39, 1431–1446. [Google Scholar] [CrossRef]
  64. Buolamwini, J.K. Cell cycle molecular targets in novel anticancer drug discovery. Curr. Pharm. Des. 2000, 6, 379–392. [Google Scholar] [CrossRef]
  65. Verma, K.A.; Singh, S. Phytochemical analysis and in vitro cytostatic potential of ethnopharmacological important medicinal plants. Toxicol. Rep. 2020, 7, 443–452. [Google Scholar] [CrossRef]
  66. Nair, A.; Manohar, S.M. A flow cytometric journey into cell cycle analysis. Bioanalysis 2021, 13, 1627–1644. [Google Scholar] [CrossRef] [PubMed]
  67. Zhang, T.; Zhao, G.; Zhu, X.; Jiang, K.; Wu, H.; Deng, G.; Qiu, C. Sodium selenite induces apoptosis via ROS-mediated NF-κB signaling and activation of the Bax–caspase-9–caspase-3 axis in 4T1 cells. J. Cell. Physiol. 2019, 234, 2511–2522. [Google Scholar] [CrossRef] [PubMed]
  68. Wu, R.; Tang, S.; Wang, M.; Xu, X.; Yao, C.; Wang, S. MicroRNA-497 induces apoptosis and suppresses proliferation via the Bcl-2/Bax-caspase9-caspase3 pathway and cyclin D2 protein in HUVECs. PLoS ONE 2016, 11, e0167052. [Google Scholar] [CrossRef] [PubMed]
  69. Nelson, V.K.; Sahoo, N.K.; Sahu, M.; Sudhan, H.H.; Pullaiah, C.P.; Muralikrishna, K.S. In vitro anticancer activity of Eclipta alba whole plant extract on colon cancer cell HCT-116. BMC Complement. Med. Ther. 2020, 20, 355. [Google Scholar] [CrossRef] [PubMed]
  70. Sinjari, B.; Pizzicannella, J.; D’Aurora, M.; Zappacosta, R.; Gatta, V.; Fontana, A.; Trubiani, O.; Diomede, F. Curcumin/Liposome Nanotechnology as Delivery Platform for Anti-inflammatory Activities via NFkB/ERK/pERK Pathway in Human Dental Pulp Treated With 2-HydroxyEthyl MethAcrylate (HEMA). Front. Physiol. 2019, 10, 633. [Google Scholar] [CrossRef]
  71. Diomede, F.; Zingariello, M.; Cavalcanti, M.F.X.B.; Merciaro, I.; Pizzicannella, J.; de Isla, N.; Caputi, S.; Ballerini, P.; Trubiani, O. MyD88/ERK/NFkB pathways and pro-inflammatory cytokines release in periodontal ligament stem cells stimulated by Porphyromonas gingivalis. Eur. J. Histochem. 2017, 61, 2791. [Google Scholar] [CrossRef]
Molecules 27 08222 g001 550
Figure 1. DPPH radical scavenging activity of J. adhatoda leaf extract. Different concentrations of J. adhatoda extract showed concentration-dependent increase in free radical scavenging activity by DPPH radical scavenging assay. One-way ANOVA test was used to perform the statistical analysis. Data represented as mean ± SD (n = 3), ** p < 0.01 vs. control; * p ≤ 0.05 and ns (non-significant) p > 0.05.
Figure 1. DPPH radical scavenging activity of J. adhatoda leaf extract. Different concentrations of J. adhatoda extract showed concentration-dependent increase in free radical scavenging activity by DPPH radical scavenging assay. One-way ANOVA test was used to perform the statistical analysis. Data represented as mean ± SD (n = 3), ** p < 0.01 vs. control; * p ≤ 0.05 and ns (non-significant) p > 0.05.
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Figure 2. Docking study with NF-κB. Docking study was conducted to assess the binding affinity of major phytoconstituents of J. adhatoda with the active site of NF-κB. The (A) 3D structure of NF-κB protein (left) spiral structure (right) space-filling model. The poses are shown for the structures of (B) Vasicine (left) 3D interaction (right) 2D interaction, (C) Vasicinol (left) 3D interaction (right) 2D interaction, (D) Vasicinone (left) 3D interaction (right) 2D interaction, (E) Deoxyvasicinone (left) 3D interaction (right) 2D interaction, (F) Vasicinolone (left) 3D interaction (right) 2D interaction.
Figure 2. Docking study with NF-κB. Docking study was conducted to assess the binding affinity of major phytoconstituents of J. adhatoda with the active site of NF-κB. The (A) 3D structure of NF-κB protein (left) spiral structure (right) space-filling model. The poses are shown for the structures of (B) Vasicine (left) 3D interaction (right) 2D interaction, (C) Vasicinol (left) 3D interaction (right) 2D interaction, (D) Vasicinone (left) 3D interaction (right) 2D interaction, (E) Deoxyvasicinone (left) 3D interaction (right) 2D interaction, (F) Vasicinolone (left) 3D interaction (right) 2D interaction.
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Figure 3. Determination of cell viability by MTT assay. Cell viability was assessed using the MTT assay for HEK-293 cells, RAW 264.7 cells, SHSY-5Y cells, MCF-7, and A549 cells treated for 24 h with various concentrations of J. adhatoda leaf extract: 50, 100, 150, 200, and 250 μg/mL (A) and for different concentrations of paclitaxel in MCF-7 cells post 24 h treatment as standard drug control (B). One-way ANOVA test was used to perform the statistical analysis, and the IC50 values of the extract on the cell lines were determined. Data represented as mean ± SD (n = 5), **** p < 0.0001 vs. control.
Figure 3. Determination of cell viability by MTT assay. Cell viability was assessed using the MTT assay for HEK-293 cells, RAW 264.7 cells, SHSY-5Y cells, MCF-7, and A549 cells treated for 24 h with various concentrations of J. adhatoda leaf extract: 50, 100, 150, 200, and 250 μg/mL (A) and for different concentrations of paclitaxel in MCF-7 cells post 24 h treatment as standard drug control (B). One-way ANOVA test was used to perform the statistical analysis, and the IC50 values of the extract on the cell lines were determined. Data represented as mean ± SD (n = 5), **** p < 0.0001 vs. control.
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Figure 4. Quantification of NO production in MCF-7 cells by Griess reagent. μM of NO production from cell supernatant of MCF-7 cell treated with 100 μg/mL and 150 μg/mL J. adhatoda leaf extract and 0.1 µM paclitaxel as standard drug. The experiment was performed in triplicate and the result presented as mean ± SD (n = 3). **** p < 0.0001 vs. control.
Figure 4. Quantification of NO production in MCF-7 cells by Griess reagent. μM of NO production from cell supernatant of MCF-7 cell treated with 100 μg/mL and 150 μg/mL J. adhatoda leaf extract and 0.1 µM paclitaxel as standard drug. The experiment was performed in triplicate and the result presented as mean ± SD (n = 3). **** p < 0.0001 vs. control.
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Figure 5. J. adhatoda leaf extract induced ROS production and mitochondrial membrane depolarization in MCF-7 cells. (A) MCF-7 cells showed elevated ROS production in a concentration-dependent manner as compared to control cells 24 h post-treatment with 100 μg/mL and 150 μg/mL of J. adhatoda leaf extract similar to 0.1 µM paclitaxel treated MCF-7 cells after staining with DCFDA. (B) Mitochondrial membrane potential was measured by confocal microscopy imaging (100x magnification) in MCF-7 cells stained with JC-1. Graphical data representing the (C) (i) mean fluorescence intensity of JC-1 monomer and JC-1 aggregates of the extract compared to control and (ii) ratio of JC-1 monomer vs. JC-1 aggregates. (D) Total GSH, free GSH, and GSSG levels in extract-treated MCF-7 cells. (E) % SOD activity. Data represented as mean ± SD (n = 3), **** p < 0.0001 vs. control, ns(non-significant) p > 0.05.
Figure 5. J. adhatoda leaf extract induced ROS production and mitochondrial membrane depolarization in MCF-7 cells. (A) MCF-7 cells showed elevated ROS production in a concentration-dependent manner as compared to control cells 24 h post-treatment with 100 μg/mL and 150 μg/mL of J. adhatoda leaf extract similar to 0.1 µM paclitaxel treated MCF-7 cells after staining with DCFDA. (B) Mitochondrial membrane potential was measured by confocal microscopy imaging (100x magnification) in MCF-7 cells stained with JC-1. Graphical data representing the (C) (i) mean fluorescence intensity of JC-1 monomer and JC-1 aggregates of the extract compared to control and (ii) ratio of JC-1 monomer vs. JC-1 aggregates. (D) Total GSH, free GSH, and GSSG levels in extract-treated MCF-7 cells. (E) % SOD activity. Data represented as mean ± SD (n = 3), **** p < 0.0001 vs. control, ns(non-significant) p > 0.05.
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Figure 6. J. adhatoda leaf extract induced apoptosis and cell cycle arrest in MCF-7 cells. (A) Early and late apoptotic cells in MCF-7 cells treated with 100 μg/mL and 150 μg/mL J. adhatoda leaf extract after staining with annexin V/PI. (B) The distribution of MCF-7 cells at the various phases of the cell cycle 24 h post-treatment with 100 μg/mL and 150 μg/mL of J. adhatoda leaf extract was determined compared to control cells. (C) Level of Bax, caspase-3, and cleaved-PARP1 analyzed by Western blotting with specific antibodies; β-actin was used as loading control. (D) Representative graph showing expression levels of caspase-3, Bax, and cleaved-PARP1. Data represented as the mean ± SD (n = 3) **** p < 0.0001 vs. control; *** p ≤ 0.001; ** p ≤ 0.01 and ns (non-significant), p > 0.05.
Figure 6. J. adhatoda leaf extract induced apoptosis and cell cycle arrest in MCF-7 cells. (A) Early and late apoptotic cells in MCF-7 cells treated with 100 μg/mL and 150 μg/mL J. adhatoda leaf extract after staining with annexin V/PI. (B) The distribution of MCF-7 cells at the various phases of the cell cycle 24 h post-treatment with 100 μg/mL and 150 μg/mL of J. adhatoda leaf extract was determined compared to control cells. (C) Level of Bax, caspase-3, and cleaved-PARP1 analyzed by Western blotting with specific antibodies; β-actin was used as loading control. (D) Representative graph showing expression levels of caspase-3, Bax, and cleaved-PARP1. Data represented as the mean ± SD (n = 3) **** p < 0.0001 vs. control; *** p ≤ 0.001; ** p ≤ 0.01 and ns (non-significant), p > 0.05.
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Figure 7. Clonogenic and wound healing assay on MCF-7 cells. (A) MCF-7 cells treated with 100 μg/mL and 150 μg/mL of J. adhatoda leaf extract showed a significant reduction in the number of colonies as compared to the control group. (B) Representative histogram showing the number of colonies. (C) Representative images of wound healing after 24 h and 48 h of treatment. (D) Representative graph showing % wound closure. Data represented as the mean ± SD of triplicate experiments **** p < 0.0001 vs. control.
Figure 7. Clonogenic and wound healing assay on MCF-7 cells. (A) MCF-7 cells treated with 100 μg/mL and 150 μg/mL of J. adhatoda leaf extract showed a significant reduction in the number of colonies as compared to the control group. (B) Representative histogram showing the number of colonies. (C) Representative images of wound healing after 24 h and 48 h of treatment. (D) Representative graph showing % wound closure. Data represented as the mean ± SD of triplicate experiments **** p < 0.0001 vs. control.
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Figure 8. Evaluation of J. adhatoda leaf extract on NF-κB p65 translocation. (A) Immunofluorescence staining images of p65 translocation in MCF-7 cells post 24 h treatment with 100 μg/mL and 150 μg/mL of J. adhatoda leaf extract, measured by confocal microscopy imaging (100· magnification). (B) Representative histogram of translocation of p65 into nucleus in MCF-7 cells. (C) The histogram representing the ratio of mean fluorescent intensity between nucleus and cytoplasm. Data represented as the mean ± SD. **** p < 0.0001 vs. control; *** p ≤ 0.001.
Figure 8. Evaluation of J. adhatoda leaf extract on NF-κB p65 translocation. (A) Immunofluorescence staining images of p65 translocation in MCF-7 cells post 24 h treatment with 100 μg/mL and 150 μg/mL of J. adhatoda leaf extract, measured by confocal microscopy imaging (100· magnification). (B) Representative histogram of translocation of p65 into nucleus in MCF-7 cells. (C) The histogram representing the ratio of mean fluorescent intensity between nucleus and cytoplasm. Data represented as the mean ± SD. **** p < 0.0001 vs. control; *** p ≤ 0.001.
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Table
Table 1. Docking score of the J. adhatoda ligands with NF-κB.
Table 1. Docking score of the J. adhatoda ligands with NF-κB.
TargetPDB IDCompounds Binding Energy (k Cal/mol)
NF-κB1LE5Vasicine−8.71
Vasicinol−8.167
Vasicinone−7.604
Deoxyvasicinone−7.56
Vasicinolone−7.141
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Kumar, S.; Singh, R.; Dutta, D.; Chandel, S.; Bhattacharya, A.; Ravichandiran, V.; Sukla, S. In Vitro Anticancer Activity of Methanolic Extract of Justicia adhatoda Leaves with Special Emphasis on Human Breast Cancer Cell Line. Molecules 2022, 27, 8222. https://doi.org/10.3390/molecules27238222

AMA Style

Kumar S, Singh R, Dutta D, Chandel S, Bhattacharya A, Ravichandiran V, Sukla S. In Vitro Anticancer Activity of Methanolic Extract of Justicia adhatoda Leaves with Special Emphasis on Human Breast Cancer Cell Line. Molecules. 2022; 27(23):8222. https://doi.org/10.3390/molecules27238222

Chicago/Turabian Style

Kumar, Sonu, Rajveer Singh, Debrupa Dutta, Shivani Chandel, Arka Bhattacharya, Velayutham Ravichandiran, and Soumi Sukla. 2022. "In Vitro Anticancer Activity of Methanolic Extract of Justicia adhatoda Leaves with Special Emphasis on Human Breast Cancer Cell Line" Molecules 27, no. 23: 8222. https://doi.org/10.3390/molecules27238222

APA Style

Kumar, S., Singh, R., Dutta, D., Chandel, S., Bhattacharya, A., Ravichandiran, V., & Sukla, S. (2022). In Vitro Anticancer Activity of Methanolic Extract of Justicia adhatoda Leaves with Special Emphasis on Human Breast Cancer Cell Line. Molecules, 27(23), 8222. https://doi.org/10.3390/molecules27238222

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