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Review

Potential Health Benefits of Olive Oil and Plant Polyphenols

by
Monika Gorzynik-Debicka
1,†,
Paulina Przychodzen
1,†,
Francesco Cappello
2,3,
Alicja Kuban-Jankowska
1,
Antonella Marino Gammazza
2,3,
Narcyz Knap
1,
Michal Wozniak
1 and
Magdalena Gorska-Ponikowska
1,4,*
1
Department of Medical Chemistry, Medical University of Gdansk, 80-211 Gdańsk, Poland
2
Department of Experimental Biomedicine and Clinical Neurosciences (BioNeC), University of Palermo, 90127 Palermo, Italy
3
Euro-Mediterranean Institute of Science and Technology (IEMEST), 90136 Palermo, Italy
4
Institute of Biomaterials and Biomolecular Systems, Department of Biophysics, University of Stuttgart, 70569 Stuttgart, Germany
*
Author to whom correspondence should be addressed.
These authors contributed equally to this work.
Int. J. Mol. Sci. 2018, 19(3), 686; https://doi.org/10.3390/ijms19030686
Submission received: 11 January 2018 / Revised: 11 February 2018 / Accepted: 25 February 2018 / Published: 28 February 2018
(This article belongs to the Special Issue Natural Bioactives and Phytochemicals in Cancer Prevention)

Abstract

:
Beneficial effects of natural plant polyphenols on the human body have been evaluated in a number of scientific research projects. Bioactive polyphenols are natural compounds of various chemical structures. Their sources are mostly fruits, vegetables, nuts and seeds, roots, bark, leaves of different plants, herbs, whole grain products, processed foods (dark chocolate), as well as tea, coffee, and red wine. Polyphenols are believed to reduce morbidity and/or slow down the development of cardiovascular and neurodegenerative diseases as well as cancer. Biological activity of polyphenols is strongly related to their antioxidant properties. They tend to reduce the pool of reactive oxygen species as well as to neutralize potentially carcinogenic metabolites. A broad spectrum of health-promoting properties of plant polyphenols comprises antioxidant, anti-inflammatory, anti-allergic, anti-atherogenic, anti-thrombotic, and anti-mutagenic effects. Scientific studies present the ability of polyphenols to modulate the human immune system by affecting the proliferation of white blood cells, and also the production of cytokines or other factors that participate in the immunological defense. The aim of the review is to focus on polyphenols of olive oil in context of their biological activities.

1. Beneficial Effects of Polyphenols

As the name suggests, polyphenols are natural, synthetic, or semisynthetic organic compounds with multiple phenolic groups in the structure. It means that polyphenols typically contain one or more aromatic rings with hydroxyl groups attached to them [1,2]. There is a growing body of evidence for beneficial roles of natural plant polyphenols in the human body. Natural bioactive polyphenols are compounds of varied chemical structures. Polyphenols are arguably the largest group of chemical substances in the plant kingdom. There are more than 8000 different polyphenolic structures known, including several hundred isolated from edible plants [3,4]. Their sources are, among others, fruits, vegetables, nuts and seeds, roots, bark, leaves of different plants, herbs, whole grain products, processed foods, as well as tea, coffee, and red wine. These compounds are characterized by a broad spectrum of biological activities. The beneficial impact of vegetables, fruits, and herbs on human health has been well known for centuries. Today, we understand the reasons for that as many plant-derived products are rich in nutrients, vitamins, minerals, and very importantly, bioactive polyphenols. Some vitamins as well as polyphenols present powerful antioxidant and anti-inflammatory properties that make them natural and efficient anticancer agents to be found in a well-balanced diet. Unlike vitamins and minerals, polyphenols are not the essential elements of the primary plant metabolism. Natural polyphenolic compounds are rather products of the secondary plant metabolism. Anyhow, they do play critical metabolic roles in the human organism [2,5,6,7].
Polyphenols were determined to reduce morbidity and/or slow down the progression of cardiovascular, neurodegenerative, and cancer diseases. The mechanism of action of polyphenols strongly relates to their antioxidant activity. Polyphenols are known to decrease the level of reactive oxygen species in the human body. Other than that, health-promoting properties of plant polyphenols comprise anti-inflammatory, anti-allergic, anti-atherogenic, anti-thrombotic, and anti-mutagenic effects [8]. There is a body of research presenting their ability to modulate the human immune system by affecting the proliferation and activity of white blood cells, as well as the production of cytokines or other factors that participate in the immunological defense [9].
A daily intake of polyphenols ranges from 0.1 to 1.0 g per day [10] with the main dietary source being fruits and vegetables, as well as herbs, spices, seasonings, coffee, tea, or wine [11]. The polyphenols of olive oil are especially interesting with respect to their well-established beneficial effects on human health and metabolism, as well as the popularity of olive oil in many different diets, and specifically the Mediterranean cuisine. Herein, we mostly focus on the anticancer properties of polyphenols available from olive oil.

2. Chemical Composition of Olive Oil

The chemical composition of olive oil varies depending on the extraction technology that is applied in order to obtain oil form the fruits (Figure 1). The process of extraction of olive oil depends on crushing olives and then separating the oil from the fruit pulp under elevated pressure. Additionally, olive oil can be extruded, post-pressured, re-pressed with or without the use of hot water. The olive oil obtained from this kind of process is usually characterized by stronger color intensity, weaker aroma, and a higher content of free fatty acids [12,13,14].
The oil obtained by chemical extraction can be used for consumption only after refining. A refining process is meant to purify the extracted oil from any residual solvent and other impurities. Refined olive oil is devoid of vitamins, polyphenols, phytosterols, and other low molecular natural ingredients [15]. Extra virgin olive oil by its low yield is more expensive than other types of olive oil, but it contains the highest level of polyphenols [16]. Due to the removal of free fatty acids, extra virgin olive oil has a delicate flavor, aroma, and light color [14,17,18,19,20,21,22,23,24]. Another interesting feature affecting virgin olive oil properties is filtration. Unfiltered olive oil preserves additional polyphenols of higher polarity that are typically lost with small amounts of water that are removed upon filtration.
Due to multiple technological processes, the content of polyphenols may vary in olive oil. Figure 1 represents the level of polyphenols in olive oil dependent on the technological process of olive oil production.
Olive oil mostly consists of triacylglycerols (98–99%). Triacylglycerols (TGA) are a diverse group of glycerol esters with different fatty acids. The predominant fatty acid present in olive oil TGAs is monounsaturated oleic acid (up to 83% w/w). There is also palmitic acid, linoleic acid, stearic acid, and palmitoleic acid making up the remainder of olive oil TGAs. There is a plethora of lipophilic or amphiphilic microconstituents present in virgin olive oil, among them, phytosterols, squalene, tocopherols, phenolic compounds, terpenic acid derivatives, etc. [26,27,28]. Phenolic compounds occur in the form of: phenolic acids or alcohols, oleuropein derivatives, lignans, and flavonoids. In olive oil, the content of polyphenols ranges from 50 to 1000 mg/kg. As a matter of fact, it depends on the agronomic factors, the ripeness of olives, as well as extraction technology, along with storage or packaging processes [29,30,31,32,33].
The flesh of healthy olives contains about 2–3% of phenolic substances in the form of glucosides and esters. Virgin olive oil contains about 500 mg/L of polyphenols. The quantity and quality of polyphenols in olive oil is closely related to the process of olive milling and further processing. Therefore, virgin olive oils have substantially higher amounts of polyphenols than refined olive oils [30,33]. The phenolic compounds in olive oil are mostly glycides (e.g., oleuropein), alcohols and phenols (tyrosol, hydroxytyrosol), and also flavonoids [26,28,34]. Phenolic compounds are mainly responsible for the characteristic gustatory property of virgin olive oil, namely the bitter taste. Some micro constituents of olive oil are soluble in water, and thus, the content of phenolic compounds that are present in olive oil depends to a large extent on the extraction process [29,34,35,36].

3. Beneficial Effects of Olive Oil and Olive Leaf Extract

Conventional medicine and phytotherapy both use olive leaf extracts to treat and prevent arterial hypertension or as diuretics and antiseptics [37,38]. Many studies on olive leaf extract showed that it is able to lower the blood pressure in animals as well as to increase blood flow through the coronary arteries, slow down the heart rate and normalize intestinal muscle contractions [37,39,40]. In clinical studies including patients with first-degree hypertension treated with olive leaf extract, the tendency to lowering the blood pressure was observed. Twice-daily dosing of 500 mg (1 g/day) of the olive leaf extract was as effective as an alternative medicine that is typically prescribed in order to lower blood pressure [41].
Recently, a chemopreventive activity of olive oil has been attributed to its unique phenolic compounds represented by phenolic alcohols like hydroxytyrosol (3,4-dihydroxyphenylethanol: 3,4-DHPEA) and tyrosol (p-hydroxyphenylethanol: p-HPEA), and their secoiridoid derivatives 3,4-DHPEA-EA (oleuropein aglycon), p-HPEA-EA (ligstroside aglycon), 3,4-DHPEA-EDA, p-HPEA-EDA (oleocanthal), and oleuropein [42].
Anticancer properties of olive oil seem to correlate with the antioxidant activity of phenolic and polyphenolic compounds present therein that are capable of scavenging free radicals and reactive oxygen species. Oleuropein, tyrosol, hydroxytyrosol, verboscoside, ligustroide, demethyleuropein were all proven to protect against the coronary artery disease [43,44,45,46] or cancer [43,47,48]. They also display antimicrobial and antiviral effects [43,49,50,51]. Antioxidant and anti-atherogenic effects of olive oil polyphenols, like oleuropein and hydroxytyrosol, have been vastly confirmed in the literature [52,53].

3.1. Health Benefits of Hydroxytyrosol

Hydroxytyrosol (HT) belongs to polyphenols, which are abundant in olives (Olea europea L.) and consequently in virgin olive oil. Its beneficial properties for human health are strongly related to the ability of the molecule to scavenge free radicals and reactive oxygen/nitrogen species as well as to activate endogenous antioxidant systems in the body. Free radical scavenging properties of HT have been convincingly confirmed in studies on rats with alloxan-induced diabetes mellitus [54].
The studies on the 3T3-L1 adipocyte cell line have shown that HT stimulates mitochondrial biosynthesis which is reduced in the course of diabetes mellitus. Most likely, HT increases mitochondrial biosynthesis pathway via upregulation of PGC-1α. Relatively low concentrations of hydroxytyrosol in adipocytes increase the expression of all mitochondrial respiratory chain complexes, including ATP synthase. HT protects mitochondria against the reduction of mitochondrial DNA synthesis, and modulates activity of the critical transcription factors, such as Nrf1 (nuclear respiratory factor 1) and Tfam (transcription factor A, mitochondrial). All of these unique properties of HT are attributed to a potential risk reduction for developing type 2 diabetes mellitus [55].

3.2. Beneficial Properties of Oleuropein

Oleuropein belongs to a group of coumarin derivative, secoiridoids [56]. It was found to be effective against various strains of bacteria, viruses, fungi and also molds or even parasites. Moreover, it inhibits platelet aggregation [57]. It is also a major constituent of a patented formulation of an endothelial proliferation inhibitor. Oral treatment with oleuropein results in a decreased number of blood vessels proving strong anti-angiogenic properties [58]. Phenolic compounds (oleuropein, protocatechuic acid) of virgin olive oil have also been shown to inhibit macrophage-mediated LDL oxidation [59]. Leaf and olive fruit extracts containing oleuropein protect insulin-producing β-cell line (INS-1) against the deleterious effect of cytokines [60].

4. Antineoplastic Properties of Olive Oil Polyphenols and the Mechanism of Action

Research has shown that some natural plant-derived polyphenols can directly or indirectly prevent cells from the initiation of neoplastic transformation due to xenobiotics and carcinogenic factors, and thus contribute to a lower risk of developing cancer. Carcinogenesis is characterized by a change in the transcriptional activity of many genes, and consequently in the biological function of the proteins that are encoded by those genes. There are many studies pointing out an essential role of polyphenolic compounds as derived from vegetables, fruits, or herbs in the regulation of epigenetic modifications, resulting in the antiproliferative protection [61]. Mechanisms of anticancer activity of olive oil polyphenols are presented in Figure 2.
Researchers reported anticancer properties of olive leaf extract in an animal skin cancer model. The extract caused cancer cell death, starting with early apoptosis and completing by the following necrosis [63,64]. Polyphenols from olive leaf extract showed synergistic effects as combined with standard chemotherapeutic agents [63].
Our studies on polyphenols of olive oil (especially oleuropein and hydroxytyrosol) also confirmed their anticancer potential on proliferation and cell death of number of cancers (osteosarcoma, neuroblastoma, breast cancer). The obtained data indicate as well the plausible synergism between polyphenols of olive oil and standard chemotherapeutics (data not published yet).
Epidemiological studies show that people of the Mediterranean region have a lower incidence of several cancers when compared to other populations [65]. The consumption of olive oil is an important factor in the Mediterranean diet, and is generally believed to be beneficial for health [66]. Olive oil consumption was proven to prevent from colorectal cancer, breast cancer and skin cancer [67,68,69]. Several mechanisms of antitumor activity of virgin olive oil have been determined. Interestingly, olive oil polyphenols were proven to protect biological membranes against oxidative modification and losing structural integrity. Similarly, polyphenolic compounds decreased oxidative damage to cellular DNA effectively decreasing promotion of colon cancer. In addition to that, HT inhibited lipooxygenase, the enzyme responsible for leukotriene synthesis, and thus modulating the inflammatory response. An alteration of the hormonal status was also observed, specifically due to antiestrogenic effects of lignans that are present in virgin olive oil [70,71].
There are pleiotropic effects of olive oil polyphenols, as observed on the molecular level. It seems however that the antioxidant potential of olive oil is the primary factor contributing to protection against cancer [72,73].
Olive oil can also protect against carcinogenic agents that are abundant in the environment and food. Again, the most important protection mechanism is alleviation of oxidative stress phenomena. It is worth mentioning that oleic acid being the major fatty acid present in olive oil TAGs is much less susceptible to oxidation than polyunsaturated acids that are abundant in seed oils. High content of antioxidant polyphenols (hydroxytyrosol, oleuropein) makes virgin olive oil relatively stable and resistant to oxidation, and thus minimizing the risk of formation of potentially carcinogenic products of lipid peroxidation upon storage. Moreover, olive oil polyphenols have been reported to induce beneficial epigenetic modifications [74] and miRNA expression pattern, lowering cancer risk [75,76].
Studies have shown that both oleuropein and hydroxytyrosol, inhibited angiogenesis and specifically endothelial tube formation by HUVEC cells on Matrigel as well as lowered migration in wound healing assays [77].

4.1. Anticancer Activity of Hydroxytyrosol

Treatment of human colon adenocarcinoma cells with olive oil polyphenols significantly inhibited cell proliferation [78,79,80]. In spite of the relatively low concentrations of hydroxytyrosol in olive oil, polyphenols are in high micromolar concentration range in the colon after gastric hydrolysis and colonic fermentation of secoiridoids that are naturally present in olive oil [81]. In colon cancer cells HT reduces epidermal growth factor receptor (EGFR) level by promoting its degradation. EGRF is one of the key receptors triggering colon carcinogenesis as it regulates the proliferation, apoptosis, angiogenesis, and invasion of cancer cells [8,82]. Moreover, HT was found to be an effective cytotoxic agent in breast cancer cell models. It inhibited cell cycle in the G0/G1 phase by decreasing the level of cyclin D1 [8,62].

4.2. Oleuropein as Anticancer Agent

There are numerous studies confirming the anticancer activity of oleuropein, as observed in human cancer cell lines, such as: breast adenocarcinoma (cell line MCF-7, MDA) [83,84,85,86,87], melanoma (cell line RPMI 7951) [86], urinary bladder carcinoma (cell line T-24) [86], colorectal adenocarcinoma (cell line HT 29, Caco-2, LoVo) [86,88,89], prostate cancer (cell line TF1) [87], lung carcinoma (cell line A549) [90], glioblastoma (cell line LN 18), renal cell adenocarcinoma (cell line 786-O) [87], and glioma (cell line U251, A172) [91].
Oleuropein was found to display antiproliferative, proapoptotic effects [92], overall anticancer activity [93], and specifically an ability to decrease cancer cell viability [94], as well as induction of cancer cell apoptosis [95,96,97,98]. Oleuropein induces apoptosis in breast cancer cells (MCF-7) via the p53-dependent pathway and through the regulation of Bax and Bcl2 genes. Therefore, oleuropein may have a great therapeutic potential for breast cancer treatment [99]. Interestingly, oleuropein has been reported to inhibit aromatase, a cytochrome P450 enzyme, which is an important pharmacological target in breast cancer therapy [100]. Moreover, it increases cancer cell sensitivity to trastuzumab (>1000-fold increase) in SKBR3/Tzb100 cell model of acquired resistance [62]. Studies in animal models have shown that oleuropein administration prevents breast cancer [87], skin cancer [101], and various soft tissue cancers [86].
Interestingly, oleuropein showed uroprotective effect against cyclophosphamide-induced hemorrhagic cystitis in a rat model mostly through its antioxidant and anti-inflammatory activities. [102]. Thus, it can be considered as a new anticancer compound for adjuvant therapy not only targeting different stages of cancer development, but also alleviating certain adverse effects in the course of cancer chemotherapy. With respect to the pronounced antioxidant properties of oleuropein, it protects cells from genetic damage, potentially leading to oncogenesis. Anti-angiogenic properties of oleuropein prevent or at least slow down tumor development [86].

5. Valuable Properties of Other Plant Polyphenols

Except from the European olive, known as Olea europea, there are many other plants rich in invaluable polyphenols. Epigallocatechin and genistein, present in tea and soy, contribute to the DNA hypomethylation, and thus reactivation of the previously suppressed suppressor genes such as p16, RARbeta, MGMT, resulting in the inhibition of cancer induction or growth [103]. Anthocyanins of black raspberries decrease DNA methyltransferase (DNMT1) activity, and also lead to the activation of the suppressor genes via promoter demethylation mechanism [104].
Other kinds of polyphenols, also classified as phytoestrogens, such as resveratrol and genistein, interact with estrogen receptors and influence the regulation of estrogen-dependent gene expression of P21 gene [105,106].
Resveratrol, as observed in animal models with chemically induced tumor lesions, showed anti-tumor and anti-atherogenic properties. On the other hand, in human tumor cell line models, resveratrol inhibited cell proliferation (cell cycle blockage) with no apoptosis induction [107]. The hydroxytyrosol-rich extracts that are available from different plants induce inhibition of breast cancer cell growth [108]. Interestingly, many studies reported ginger (Zingiber officinale Roscoe) to contain numerous chemical constituents of potential health benefits. According to some, pulp and peel of ginger rhizomes exhibit in vitro antiproliferative activity against colon cancer cells. They also show anti-inflammatory properties due to inhibition of cellular nitric oxide production. The anticancer activity of ginger rhizome against colorectal carcinoma is attributed to the main compound of the extract—α-zingiberene and its derivatives [109]. In addition to that, 6-shogaol, another phenolic constituent of ginger, decreased metastatic potential of lung and breast cancer in mice. Studies confirm that 6-shogaol exerts significant anticancer activity both in vivo and in vitro, and at present is concerned as an efficacious immunotherapeutic agent for cancer treatment [110].
Other noteworthy polyphenols are chlorogenic and caffeic acids that are found in coffee and other plants. They are both powerful antioxidants as observed in vitro and they effectively inhibit N-nitrosation reaction, as observed in vivo. Furthermore, chlorogenic acid can inhibit DNA damage as observed in vitro since it inhibits lipid peroxidation and suppresses reactive oxygen species-mediated nuclear factor NF-κB [111,112,113]. Interestingly, recent studies have demonstrated a reciprocal relationship between coffee intake and the risk of colon, liver, breast, or endometrial cancer. It was found that the consumption of at least one cup of coffee per day lowered the risk of upper gastrointestinal cancer in the Japanese population by 49% [111,114]. There are, without doubt, plants containing numerous chemicals invaluable for human health that are still waiting to be discovered.

6. Conclusions

Beneficial roles of natural plant polyphenols in the human body have been known for ages. Their sources are fresh fruits, vegetables and certain processed plant foods. Polyphenols have been reported to reduce morbidity and slow down the progression of cardiovascular, neurodegenerative and cancer diseases. Figure 3 presents a wide range of different benefits of olive oil polyphenols.
The action mechanism of polyphenols is pleiotropic, however, it mostly relates to their antioxidant activity. Natural polyphenols decrease the level of reactive oxygen species protecting biomolecules against oxidative damage. They are also found to modulate the human immune system, affecting proliferation of the white blood cells and the production of cytokines.
Oleuropein, hydroxytyrosol, and their derivatives are polyphenolic compounds that are abundant in olive oil. They are powerful antioxidants displaying anticancer, anti-angiogenic and anti-inflammatory properties.
It should be emphasized that the unique properties of olive oil polyphenols have been evaluated mostly based on in vitro models. In order to verify their beneficial impact on human health, more in vivo studies and well-designed clinical trials are still necessary. Nonetheless, the preliminary results seem to be pretty encouraging in terms of prevention and treatment of cancer or cardiovascular and neurodegenerative diseases.
An increase in consumption of virgin olive oil and other plant products rich in polyphenolic compounds, specifically in populations with low olive oil intake, does seem to be rational and provide diverse health benefits.

Acknowledgments

The manuscript and studies concerning anticancer influence of polyphenols of olive oil were funded by the MN grant No. 01-0276/08/259 from Medical University of Gdansk (Gdansk, Poland) and Polish Ministry of Science and Higher Education. The authors kindly thank Prof. Stephan Nussberger (Institute of Biomaterials and Biomolecular Systems, Department of Biophysics, University of Stuttgart, Stuttgart, Germany) for his valuable comments on our article.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Bravo, L. Polyphenols: Chemistry, dietary sources, metabolism, and nutritional significance. Nutr. Rev. 1998, 56, 317–333. [Google Scholar] [CrossRef] [PubMed]
  2. Del Rio, D.; Rodriguez-Mateos, A.; Spencer, J.P.; Tognolini, M.; Borges, G.; Crozier, A. Dietary (poly) phenolics in human health: Structures, bioavailability, and evidence of protective effects against chronic diseases. Antioxid. Redox Signal. 2013, 18, 1818–1892. [Google Scholar] [CrossRef] [PubMed]
  3. Pandey, K.B.; Rizvi, S.I. Plant polyphenols as dietary antioxidants in human health and disease. Oxid. Med. Cell. Longev. 2009, 2, 270–278. [Google Scholar] [CrossRef] [PubMed]
  4. Ross, J.A.; Kasum, C.M. Dietary flavonoids: Bioavailability, metabolic effects, and safety. Annu. Rev. Nutr. 2002, 22, 19–34. [Google Scholar] [CrossRef] [PubMed]
  5. Cicerale, S.; Conlan, X.A.; Sinclair, A.J.; Keast, R.S. Chemistry and health of olive oil phenolics. Crit. Rev. Food Sci. Nutr. 2008, 49, 218–236. [Google Scholar] [CrossRef] [PubMed]
  6. Cicerale, S.; Lucas, L.; Keast, R. Biological activities of phenolic compounds present in virgin olive oil. Int. J. Mol. Sci. 2010, 11, 458–479. [Google Scholar] [CrossRef] [PubMed]
  7. Boss, A.; Bishop, K.S.; Marlow, G.; Barnett, M.P.; Ferguson, L.R. Evidence to support the Anti-Cancer effect of olive leaf extract and future Directions. Nutrients 2016, 8, 513. [Google Scholar] [CrossRef] [PubMed]
  8. Ellis, L.Z.; Liu, W.; Luo, Y.; Okamoto, M.; Qu, D.; Dunn, J.H.; Fujita, M. Green tea polyphenol epigallocatechin-3-gallate suppresses melanoma growth by inhibiting inflammasome and IL-1β secretion. Biochem. Biophys. Res. Commun. 2011, 414, 551–556. [Google Scholar] [CrossRef] [PubMed]
  9. John, C.M.; Sandrasaigaran, P.; Tong, C.K.; Adam, A.; Ramasamy, R. Immunomodulatory activity of polyphenols derived from Cassia auriculata flowers in aged rats. Cell. Immunol. 2011, 271, 474–479. [Google Scholar] [CrossRef] [PubMed]
  10. Panickar, K.S.; Anderson, R.A. Effect of polyphenols on oxidative stress and mitochondrial dysfunction in neuronal death and brain edema in cerebral ischemia. Int. J. Mol. Sci. 2011, 12, 8181–8207. [Google Scholar] [CrossRef] [PubMed]
  11. Han, X.; Shen, T.; Lou, H. Dietary polyphenols and their biological significance. Int. J. Mol. Sci. 2007, 8, 950–988. [Google Scholar] [CrossRef]
  12. Gökçebağ, M.; Dıraman, H.; Özdemir, D. Classification of Turkish Monocultivar (Ayvalık and Memecik cv.) Virgin Olive Oils from north and south zones of Aegean region based on their triacyglycerol profiles. J. Am. Oil Chem. Soc. 2013, 90, 1661–1671. [Google Scholar] [CrossRef]
  13. Ozkaya, M.T.; Ergulen, E.; Ulger, S.; Ozilbey, N. Genetic and biologic characterization of some olive (Olea europaea L.) cultivars grown in Turkey. J. Agric. Sci. Ankara Univ. 2004, 10, 231–236. [Google Scholar]
  14. Fernández, A.G.; Adams, M.R.; Fernández-Díez, M. Table Olives: Production and Processing; Springer: Berlin, Germany, 1997. [Google Scholar]
  15. Kamm, W.; Dionisi, F.; Hischenhuber, C.; Engel, K.-H. Authenticity assessment of fats and oils. Food Rev. Int. 2001, 17, 249–290. [Google Scholar] [CrossRef]
  16. Kalogeropoulos, N.; Tsimidou, M.Z. Antioxidants in Greek virgin olive oils. Antioxidants 2014, 3, 387–413. [Google Scholar] [CrossRef] [PubMed]
  17. Fragaki, G.; Spyros, A.; Siragakis, G.; Salivaras, E.; Dais, P. Detection of extra virgin olive oil adulteration with lampante olive oil and refined olive oil using nuclear magnetic resonance spectroscopy and multivariate statistical analysis. J. Agric. Food Chem. 2005, 53, 2810–2816. [Google Scholar] [CrossRef] [PubMed]
  18. Grossi, M.; Di Lecce, G.; Toschi, T.G.; Riccò, B. Fast and accurate determination of olive oil acidity by electrochemical impedance spectroscopy. IEEE Sens. J. 2014, 14, 2947–2954. [Google Scholar] [CrossRef]
  19. Luna, G.; Morales, M.; Aparicio, R. Changes induced by UV radiation during virgin olive oil storage. J. Agric. Food Chem. 2006, 54, 4790–4794. [Google Scholar] [CrossRef] [PubMed]
  20. Angerosa, F. Influence of volatile compounds on virgin olive oil quality evaluated by analytical approaches and sensor panels. Eur. J. Lipid Sci. Technol. 2002, 104, 639–660. [Google Scholar] [CrossRef]
  21. Youssef, O.; Guido, F.; Mokhar, G.; Nabil, B.Y.; Daoud, D.; Mokhtar, Z. The compositional quality and volatile compounds of samples from the blend of monovarietal olive oils cultivated in Tunisia. Int. J. Food Sci. Technol. 2011, 46, 678–686. [Google Scholar] [CrossRef]
  22. Kesen, S.; Kelebek, H.; Selli, S. Characterization of the volatile, phenolic and antioxidant properties of monovarietal olive oil obtained from cv. Halhali. J. Am. Oil Chem. Soc. 2013, 90, 1685–1696. [Google Scholar] [CrossRef]
  23. Šarolić, M.; Gugić, M.; Friganović, E.; Tuberoso, C.I.G.; Jerković, I. Phytochemicals and other characteristics of Croatian monovarietal extra virgin olive oils from Oblica, Lastovka and Levantinka varieties. Molecules 2015, 20, 4395–4409. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  24. Lynch, B.; Rozema, A. Olive Oil: Conditions of Competition between Us and Major Foreign Supplier Industries; United States International Trade Commission: Washington, DC, USA, 2013. [Google Scholar]
  25. Types of Olive Oil. Available online: http://www.nuproas.se/nuproas/olive/types-of-olive-oil/ (accesed on 26 February 2018.
  26. Boskou, D. Other important minor constituents. In Olive Oil: Minorconstituents and Health; CRC Press: Boca Raton, FL, USA, 2009; pp. 45–54. [Google Scholar]
  27. Luchetti, F. Importance and future of olive oil in the world market—An introduction to olive oil. Eur. J. Lipid Sci. Technol. 2002, 104, 559–563. [Google Scholar] [CrossRef]
  28. Ramirez-Tortosa, M.C.; Granados, S.; Quiles, J.L. Chemical composition, types and characteristics of olive oil. Olive Oil Health 2006, 45–61. [Google Scholar] [CrossRef]
  29. Tuck, K.L.; Hayball, P.J. Major phenolic compounds in olive oil: Metabolism and health effects. J. Nutr. Biochem. 2002, 13, 636–644. [Google Scholar] [CrossRef]
  30. Naczk, M.; Shahidi, F. Extraction and analysis of phenolics in food. J. Chromatogr. A 2004, 1054, 95–111. [Google Scholar] [CrossRef]
  31. Litridou, M.; Linssen, J.; Schols, H.; Bergmans, M.; Posthumus, M.; Tsimidou, M.; Boskou, D. Phenolic compounds in virgin olive oils: Fractionation by solid phase extraction and antioxidant activity assessment. J. Sci. Food Agric. 1997, 74, 169–174. [Google Scholar] [CrossRef]
  32. Baldioli, M.; Servili, M.; Perretti, G.; Montedoro, G. Antioxidant activity of tocopherols and phenolic compounds of virgin olive oil. J. Am. Oil Chem. Soc. 1996, 73, 1589–1593. [Google Scholar] [CrossRef]
  33. Bianco, A.; Coccioli, F.; Guiso, M.; Marra, C. The occurrence in olive oil of a new class of phenolic compounds: Hydroxy-isochromans. Food Chem. 2002, 77, 405–411. [Google Scholar] [CrossRef]
  34. Boskou, D.; Blekas, G.; Tsimidou, M. Olive oil composition. In Olive Oil: Chemistry and Technology; American Oil Chemists’ Society Press: Champaign, IL, USA, 2006; Volume 4. [Google Scholar]
  35. Firestone, D. Olive oil. In Bailey’s Industrial Oil and Fat Products; John Wiley & Sons: Hoboken, NJ, USA, 2005. [Google Scholar]
  36. Visioli, F.; Grande, S.; Bogani, P.; Galli, C.; Quiles, J.; Ramirez-Tortosa, M.; Yaqoob, P. Antioxidant properties of olive oil phenolics. In Olive Oil Health; CABI Publishing: Oxford, UK, 2006; pp. 109–118. [Google Scholar]
  37. Ferreira, I.C.; Barros, L.; Soares, M.E.; Bastos, M.L.; Pereira, J.A. Antioxidant activity and phenolic contents of Olea europaea L. leaves sprayed with different copper formulations. Food Chem. 2007, 103, 188–195. [Google Scholar] [CrossRef]
  38. Gryszczyńska, A.; Gryszczyńska, B.; Opala, B. The leaves of european olive (Olea europaea L.)—Chemistry and application in medicine. Postępy Fitoterapii 2010, 11, 30–37. [Google Scholar]
  39. Samuelsson, G. The blood pressure lowering factor in leaves of Olea europaea. Farmacevtisk Revy 1951, 15, 229–239. [Google Scholar]
  40. Zarzuelo, A.; Duarte, J.; Jimenez, J.; Gonzalez, M.; Utrilla, M. Vasodilator effect of olive leaf. Planta Med. 1991, 57, 417–419. [Google Scholar] [CrossRef] [PubMed]
  41. Susalit, E.; Agus, N.; Effendi, I.; Tjandrawinata, R.R.; Nofiarny, D.; Perrinjaquet-Moccetti, T.; Verbruggen, M. Olive (Olea europaea) leaf extract effective in patients with stage-1 hypertension: Comparison with Captopril. Phytomedicine 2011, 18, 251–258. [Google Scholar] [CrossRef] [PubMed]
  42. Fabiani, R. Anti-cancer properties of olive oil secoiridoid phenols: A systematic review of in vivo studies. Food Funct. 2016, 7, 4145–4159. [Google Scholar] [CrossRef] [PubMed]
  43. Malik, N.S.; Bradford, J.M. Changes in oleuropein levels during differentiation and development of floral buds in ‘Arbequina’olives. Sci. Horticult. 2006, 110, 274–278. [Google Scholar] [CrossRef]
  44. Manna, C.; D’Angelo, S.; Migliardi, V.; Loffredi, E.; Mazzoni, O.; Morrica, P.; Galletti, P.; Zappia, V. Protective effect of the phenolic fraction from virgin olive oils against oxidative stress in human cells. J. Agric. Food Chem. 2002, 50, 6521–6526. [Google Scholar] [CrossRef] [PubMed]
  45. Visioli, F.; Bellosta, S.; Galli, C. Oleuropein, the bitter principle of olives, enhances nitric oxide production by mouse macrophages. Life Sci. 1998, 62, 541–546. [Google Scholar] [CrossRef]
  46. Wiseman, S.A.; Mathot, J.N.; de Fouw, N.J.; Tijburg, L.B. Dietary non-tocopherol antioxidants present in extra virgin olive oil increase the resistance of low density lipoproteins to oxidation in rabbits. Atherosclerosis 1996, 120, 15–23. [Google Scholar] [CrossRef]
  47. Owen, R.; Giacosa, A.; Hull, W.; Haubner, R.; Spiegelhalder, B.; Bartsch, H. The antioxidant/anticancer potential of phenolic compounds isolated from olive oil. Eur. J. Cancer 2000, 36, 1235–1247. [Google Scholar] [CrossRef]
  48. Tripoli, E.; Giammanco, M.; Tabacchi, G.; Di Majo, D.; Giammanco, S.; la Guardia, M. The phenolic compounds of olive oil: Structure, biological activity and beneficial effects on human health. Nutr. Res. Rev. 2005, 18, 98–112. [Google Scholar] [CrossRef] [PubMed]
  49. Bisignano, G.; Tomaino, A.; Cascio, R.L.; Crisafi, G.; Uccella, N.; Saija, A. On the in-vitro antimicrobial activity of oleuropein and hydroxytyrosol. J. Pharm. Pharmacol. 1999, 51, 971–974. [Google Scholar] [CrossRef] [PubMed]
  50. Fleming, H.; Walter, W.; Etchells, J. Antimicrobial properties of oleuropein and products of its hydrolysis from green olives. Appl. Microbiol. 1973, 26, 777–782. [Google Scholar] [PubMed]
  51. Federici, F.; Bongi, G. Improved method for isolation of bacterial inhibitors from oleuropein hydrolysis. Appl. Environ. Microbiol. 1983, 46, 509–510. [Google Scholar] [PubMed]
  52. Carluccio, M.A.; Siculella, L.; Ancora, M.A.; Massaro, M.; Scoditti, E.; Storelli, C.; Visioli, F.; Distante, A.; de Caterina, R. Olive oil and red wine antioxidant polyphenols inhibit endothelial activation. Arterioscler. Thromb. Vasc. Biol. 2003, 23, 622–629. [Google Scholar] [CrossRef] [PubMed]
  53. Edgecombe, S.C.; Stretch, G.L.; Hayball, P.J. Oleuropein, an antioxidant polyphenol from olive oil, is poorly absorbed from isolated perfused rat intestine. J. Nutr. 2000, 130, 2996–3002. [Google Scholar] [CrossRef] [PubMed]
  54. Jemai, H.; El Feki, A.; Sayadi, S. Antidiabetic and antioxidant effects of hydroxytyrosol and oleuropein from olive leaves in alloxan-diabetic rats. J. Agric. Food Chem. 2009, 57, 8798–8804. [Google Scholar] [CrossRef] [PubMed]
  55. Hao, J.; Shen, W.; Yu, G.; Jia, H.; Li, X.; Feng, Z.; Wang, Y.; Weber, P.; Wertz, K.; Sharman, E. Hydroxytyrosol promotes mitochondrial biogenesis and mitochondrial function in 3T3-L1 adipocytes. J. Nutr. Biochem. 2010, 21, 634–644. [Google Scholar] [CrossRef] [PubMed]
  56. Soler-Rivas, C.; Espín, J.C.; Wichers, H.J. Oleuropein and related compounds. J. Sci. Food Agric. 2000, 80, 1013–1023. [Google Scholar] [CrossRef]
  57. Benavente-Garcıa, O.; Castillo, J.; Lorente, J.; Ortuno, A.; del Rio, J. Antioxidant activity of phenolics extracted from Olea europaea L. leaves. Food Chem. 2000, 68, 457–462. [Google Scholar] [CrossRef]
  58. Hamdi, H.K.; Tavis, J.H.; Castellon, R. Methods for Inhibiting Angiogenesis. Patent WO/2002/094193, 28 November 2002. [Google Scholar]
  59. Masella, R.; Varì, R.; D’Archivio, M.; di Benedetto, R.; Matarrese, P.; Malorni, W.; Scazzocchio, B.; Giovannini, C. Extra virgin olive oil biophenols inhibit cell-mediated oxidation of LDL by increasing the mRNA transcription of glutathione-related enzymes. J. Nutr. 2004, 134, 785–791. [Google Scholar] [CrossRef] [PubMed]
  60. Cumaoğlu, A.; Ari, N.; Kartal, M.; Karasu, Ç. Polyphenolic extracts from Olea europea L. protect against cytokine-induced β-cell damage through maintenance of redox homeostasis. Rejuv. Res. 2011, 14, 325–334. [Google Scholar] [CrossRef] [PubMed]
  61. Stefanska, B.; Karlic, H.; Varga, F.; Fabianowska-Majewska, K.; Haslberger, A. Epigenetic mechanisms in anti-cancer actions of bioactive food components–the implications in cancer prevention. Br. J. Pharmacol. 2012, 167, 279–297. [Google Scholar] [CrossRef] [PubMed]
  62. Rigacci, S.; Stefani, M. Nutraceutical properties of olive oil polyphenols. An itinerary from cultured cells through animal models to humans. Int. J. Mol. Sci. 2016, 17, 843. [Google Scholar] [CrossRef] [PubMed]
  63. Mijatovic, S.A.; Timotijevic, G.S.; Miljkovic, D.M.; Radovic, J.M.; Maksimovic-Ivanic, D.D.; Dekanski, D.P.; Stosic-Grujicic, S.D. Multiple antimelanoma potential of dry olive leaf extract. Int. J. Cancer 2011, 128, 1955–1965. [Google Scholar] [CrossRef] [PubMed]
  64. Bhatia, S.; Tykodi, S.S.; Thompson, J.A. Treatment of metastatic melanoma: An overview. Oncology 2009, 23, 488. [Google Scholar] [PubMed]
  65. Gotsis, E.; Anagnostis, P.; Mariolis, A.; Vlachou, A.; Katsiki, N.; Karagiannis, A. Health benefits of the Mediterranean diet: An update of research over the last 5 years. Angiology 2015, 66, 304–318. [Google Scholar] [CrossRef] [PubMed]
  66. Owen, R.; Haubner, R.; Würtele, G.; Hull, W.; Spiegelhalder, B.; Bartsch, H. Olives and olive oil in cancer prevention. Eur. J. Cancer Prev. 2004, 13, 319–326. [Google Scholar] [CrossRef] [PubMed]
  67. Psaltopoulou, T.; Kosti, R.I.; Haidopoulos, D.; Dimopoulos, M.; Panagiotakos, D.B. Olive oil intake is inversely related to cancer prevalence: A systematic review and a meta-analysis of 13,800 patients and 23,340 controls in 19 observational studies. Lipids Health Dis. 2011, 10, 127. [Google Scholar] [CrossRef] [PubMed]
  68. López de las Hazas, M.-C.; Piñol, C.; Macià, A.; Motilva, M.-J. Hydroxytyrosol and the colonic metabolites derived from virgin olive oil intake induce cell cycle arrest and apoptosis in colon cancer cells. J. Agric. Food Chem. 2017, 65, 6467–6476. [Google Scholar] [CrossRef] [PubMed]
  69. Owen, R.W.; Giacosa, A.; Hull, W.E.; Haubner, R.; Würtele, G.; Spiegelhalder, B.; Bartsch, H. Olive-oil consumption and health: The possible role of antioxidants. Lancet Oncol. 2000, 1, 107–112. [Google Scholar] [CrossRef]
  70. Nan, J.; Ververis, K.; Bollu, S.; Rodd, A.; Swarup, O.; Karagiannis, T. Biological effects of the olive polyphenol, hydroxytyrosol: An extra view from genome-wide transcriptome analysis. Hellenic J. Nucl. Med. 2013, 17, 62–69. [Google Scholar]
  71. Escrich, E.; Moral, R.; Grau, L.; Costa, I.; Solanas, M. Molecular mechanisms of the effects of olive oil and other dietary lipids on cancer. Mol. Nutr. Food Res. 2007, 51, 1279–1292. [Google Scholar] [CrossRef] [PubMed]
  72. Visioli, F.; Galli, C.; Bornet, F.; Mattei, A.; Patelli, R.; Galli, G.; Caruso, D. Olive oil phenolics are dose-dependently absorbed in humans. FEBS Lett. 2000, 468, 159–160. [Google Scholar] [CrossRef]
  73. Jenner, P.; Olanow, C.W. Oxidative stress and the pathogenesis of Parkinson’s disease. Neurology 1996, 47, 161S–170S. [Google Scholar] [CrossRef]
  74. Caramia, G.; Gori, A.; Valli, E.; Cerretani, L. Virgin olive oil in preventive medicine: From legend to epigenetics. Eur. J. Lipid Sci. Technol. 2012, 114, 375–388. [Google Scholar] [CrossRef]
  75. Tunca, B.; Tezcan, G.; Cecener, G.; Egeli, U.; Ak, S.; Malyer, H.; Tumen, G.; Bilir, A. Olea europaea leaf extract alters microRNA expression in human glioblastoma cells. J. Cancer Res. Clin. Oncol. 2012, 138, 1831–1844. [Google Scholar] [CrossRef] [PubMed]
  76. D’Amore, S.; Vacca, M.; Cariello, M.; Graziano, G.; D’Orazio, A.; Salvia, R.; Sasso, R.C.; Sabbà, C.; Palasciano, G.; Moschetta, A. Genes and miRNA expression signatures in peripheral blood mononuclear cells in healthy subjects and patients with metabolic syndrome after acute intake of extra virgin olive oil. BBA-Mol. Cell Biol. Lipids 2016, 1861, 1671–1680. [Google Scholar] [CrossRef] [PubMed]
  77. Scoditti, E.; Calabriso, N.; Massaro, M.; Pellegrino, M.; Storelli, C.; Martines, G.; de Caterina, R.; Carluccio, M.A. Mediterranean diet polyphenols reduce inflammatory angiogenesis through MMP-9 and COX-2 inhibition in human vascular endothelial cells: A potentially protective mechanism in atherosclerotic vascular disease and cancer. Arch. Biochem. Biophys. 2012, 527, 81–89. [Google Scholar] [CrossRef] [PubMed]
  78. Gill, C.I.R.; Boyd, A.; McDermott, E.; McCann, M.; Servili, M.; Selvaggini, R.; Taticchi, A.; Esposto, S.; Montedoro, G.; McGlynn, H.; et al. Potential anti-cancer effects of virgin olive oil phenolson colorectal carcinogenesis models in vitro. Int. J. Cancer 2005, 117, 1–7. [Google Scholar] [CrossRef] [PubMed]
  79. Hashim, Y.Z.H.-Y.; Worthington, J.; Allsopp, P.; Ternan, N.G.; Brown, E.M.; McCann, M.J.; Rowland, I.R.; Esposto, S.; Servili, M.; Gill, C.I.R.; et al. Virgin olive oil phenolics extract inhibit invasion of HT115 human colon cancer cells in vitro and in vivo. Food Funct. 2014, 5, 1513. [Google Scholar] [CrossRef] [PubMed]
  80. Hashim, Y.Z.Y.; Rowland, I.R.; McGlynn, H.; Servili, M.; Selvaggini, R.; Taticchi, A.; Esposto, S.; Montedoro, G.; Kaisalo, L.; Wähälä, K.; et al. Inhibitory effects of olive oil phenolics on invasion in human colon adenocarcinoma cells in vitro. Int. J. Cancer 2008, 122, 495–500. [Google Scholar] [CrossRef] [PubMed]
  81. Corona, G.; Tzounis, X.; Assunta Dessi, M.; Deiana, M.; Debnam, E.S.; Visioli, F.; Spencer, J.P. The fate of olive oil polyphenols in the gastrointestinal tract: Implications of gastric and colonic microflora-dependent biotransformation. Free Radic. Res. 2006, 40, 647–658. [Google Scholar] [CrossRef] [PubMed]
  82. Terzuoli, E.; Giachetti, A.; Ziche, M.; Donnini, S. Hydroxytyrosol, a product from olive oil, reduces colon cancer growth by enhancing epidermal growth factor receptor degradation. Mol. Nutr. Food Res. 2015, 60, 519–529. [Google Scholar] [CrossRef] [PubMed]
  83. Fayyaz, S.; Aydin, T.; Cakir, A.; Gasparri, M.L.; Benedetti Panici, P.; Ahmad Farooqi, A. Oleuropein mediated targeting of signaling network in cancer. Curr. Top. Med. Chem. 2016, 16, 2477–2483. [Google Scholar] [CrossRef] [PubMed]
  84. Goulas, V.; Exarchou, V.; Troganis, A.N.; Psomiadou, E.; Fotsis, T.; Briasoulis, E.; Gerothanassis, I.P. Phytochemicals in olive-leaf extracts and their antiproliferative activity against cancer and endothelial cells. Mol. Nutr. Food Res. 2009, 53, 600–608. [Google Scholar] [CrossRef] [PubMed]
  85. Han, J.; Talorete, T.P.; Yamada, P.; Isoda, H. Anti-proliferative and apoptotic effects of oleuropein and hydroxytyrosol on human breast cancer MCF-7 cells. Cytotechnology 2009, 59, 45–53. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  86. Hamdi, H.K.; Castellon, R. Oleuropein, a non-toxic olive iridoid, is an anti-tumor agent and cytoskeleton disruptor. Biochem. Biophys. Res. Commun. 2005, 334, 769–778. [Google Scholar] [CrossRef] [PubMed]
  87. Sepporta, M.V.; Fuccelli, R.; Rosignoli, P.; Ricci, G.; Servili, M.; Morozzi, G.; Fabiani, R. Oleuropein inhibits tumour growth and metastases dissemination in ovariectomised nude mice with MCF-7 human breast tumour xenografts. J. Funct. Foods 2014, 8, 269–273. [Google Scholar] [CrossRef]
  88. Cárdeno, A.; Sánchez-Hidalgo, M.; Cortes-Delgado, A.; Alarcón de la Lastra, C. Mechanisms involved in the antiproliferative and proapoptotic effects of unsaponifiable fraction of extra virgin olive oil on HT-29 cancer cells. Nutr. Cancer 2013, 65, 908–918. [Google Scholar] [CrossRef] [PubMed]
  89. Corona, G.; Deiana, M.; Incani, A.; Vauzour, D.; Dessì, M.A.; Spencer, J.P. Inhibition of p38/CREB phosphorylation and COX-2 expression by olive oil polyphenols underlies their anti-proliferative effects. Biochem. Biophys. Res. Commun. 2007, 362, 606–611. [Google Scholar] [CrossRef] [PubMed]
  90. Mao, W.; Shi, H.; Chen, X.; Yin, Y.; Yang, T.; Ge, M.; Luo, M.; Chen, D.; Qian, X. Anti-proliferation and migration effects of oleuropein on human A549 lung carcinoma cells. Lat. Am. J. Pharm. 2012, 31, 1217–1221. [Google Scholar]
  91. Liu, M.; Wang, J.; Huang, B.; Chen, A.; Li, X. Oleuropein inhibits the proliferation and invasion of glioma cells via suppression of the AKT signaling pathway. Oncol. Rep. 2016, 36, 2009–2016. [Google Scholar] [CrossRef] [PubMed]
  92. Casaburi, I.; Puoci, F.; Chimento, A.; Sirianni, R.; Ruggiero, C.; Avena, P.; Pezzi, V. Potential of olive oil phenols as chemopreventive and therapeutic agents against cancer: A review of in vitro studies. Mol. Nutr. Food Res. 2013, 57, 71–83. [Google Scholar] [CrossRef] [PubMed]
  93. Hassan, Z.K.; Elamin, M.H.; Daghestani, M.H.; Omer, S.A.; Al-Olayan, E.M.; Elobeid, M.A.; Virk, P.; Mohammed, O.B. Oleuropein induces anti-metastatic effects in breast cancer. Asian Pac. J. Cancer Prev. 2012, 13, 4555–4559. [Google Scholar] [CrossRef] [PubMed]
  94. Menendez, J.A.; Vazquez-Martin, A.; Colomer, R.; Brunet, J.; Carrasco-Pancorbo, A.; Garcia-Villalba, R.; Fernandez-Gutierrez, A.; Segura-Carretero, A. Olive oil’s bitter principle reverses acquired autoresistance to trastuzumab (Herceptin™) in HER2-overexpressing breast cancer cells. BMC Cancer 2007, 7, 80. [Google Scholar] [CrossRef] [PubMed]
  95. Campolo, M.; di Paola, R.; Impellizzeri, D.; Crupi, R.; Morittu, V.M.; Procopio, A.; Perri, E.; Britti, D.; Peli, A.; Esposito, E. Effects of a polyphenol present in olive oil, oleuropein aglycone, in a murine model of intestinal ischemia/reperfusion injury. J. Leukoc. Biol. 2013, 93, 277–287. [Google Scholar] [CrossRef] [PubMed]
  96. Elamin, M.H.; Daghestani, M.H.; Omer, S.A.; Elobeid, M.A.; Virk, P.; Al-Olayan, E.M.; Hassan, Z.K.; Mohammed, O.B.; Aboussekhra, A. Olive oil oleuropein has anti-breast cancer properties with higher efficiency on ER-negative cells. Food Chem. Toxicol. 2013, 53, 310–316. [Google Scholar] [CrossRef] [PubMed]
  97. Oi-Kano, Y.; Kawada, T.; Watanabe, T.; Koyama, F.; Watanabe, K.; Senbongi, R.; Iwai, K. Oleuropein supplementation increases urinary noradrenaline and testicular testosterone levels and decreases plasma corticosterone level in rats fed high-protein diet. J. Nutr. Biochem. 2013, 24, 887–893. [Google Scholar] [CrossRef] [PubMed]
  98. Pasban-Aliabadi, H.; Esmaeili-Mahani, S.; Sheibani, V.; Abbasnejad, M.; Mehdizadeh, A.; Yaghoobi, M.M. Inhibition of 6-hydroxydopamine-induced PC12 cell apoptosis by olive (Olea europaea L.) leaf extract is performed by its main component oleuropein. Rejuv. Res. 2013, 16, 134–142. [Google Scholar] [CrossRef] [PubMed]
  99. Hassan, Z.K.; Elamin, M.H.; Omer, S.A.; Daghestani, M.H.; Al-Olayan, E.S.; Elobeid, M.A.; Virk, P. Oleuropein induces apoptosis via the p53 pathway in breast cancer cells. Asian Pac. J. Cancer Prev. 2013, 14, 6739–6742. [Google Scholar] [CrossRef]
  100. Neves, M.A.; Dinis, T.C.; Colombo, G.; Sá, E.; Melo, M.L. Combining computational and biochemical studies for a rationale on the anti-aromatase activity of natural polyphenols. ChemMedChem 2007, 2, 1750–1762. [Google Scholar] [CrossRef] [PubMed]
  101. Kimura, Y.; Sumiyoshi, M. Olive leaf extract and its main component oleuropein prevent chronic ultraviolet B radiation-induced skin damage and carcinogenesis in hairless mice. J. Nutr. 2009, 139, 2079–2086. [Google Scholar] [CrossRef] [PubMed]
  102. Sherif, I.O.; Nakshabandi, Z.M.; Mohamed, M.A.; Sarhan, O.M. Uroprotective effect of oleuropein in a rat model of hemorrhagic cystitis. Int. J. Biochem. Cell Biol. 2016, 74, 12–17. [Google Scholar] [CrossRef] [PubMed]
  103. Fang, M.Z.; Chen, D.; Sun, Y.; Jin, Z.; Christman, J.K.; Yang, C.S. Reversal of hypermethylation and reactivation of p16INK4a, RARβ, and MGMT genes by genistein and other isoflavones from soy. Clin. Cancer Res. 2005, 11, 7033–7041. [Google Scholar] [CrossRef] [PubMed]
  104. Wang, L.-S.; Arnold, M.; Huang, Y.-W.; Sardo, C.; Seguin, C.; Martin, E.W.; Huang, T.H.-M.; Riedl, K.; Schwartz, S.J.; Frankel, W.L. Modulation of genetic and epigenetic biomarkers of colorectal cancer in humans by black raspberries: A phase I pilot study. Clin. Cancer Res. 2011, 17, 598–610. [Google Scholar] [CrossRef] [PubMed]
  105. Mandal, S.; Davie, J.R. Estrogen regulated expression of the p21Waf1/Cip1 gene in estrogen receptor positive human breast cancer cells. J. Cell. Physiol. 2010, 224, 28–32. [Google Scholar] [PubMed]
  106. Pozo-Guisado, E.; Lorenzo-Benayas, M.J.; Fernández-Salguero, P.M. Resveratrol modulates the phosphoinositide 3-kinase pathway through an estrogen receptor α-dependent mechanism: Relevance in cell proliferation. Int. J. Cancer 2004, 109, 167–173. [Google Scholar] [CrossRef] [PubMed]
  107. Ullah, M.F.; Khan, M.W. Food as medicine: Potential therapeutic tendencies of plant derived polyphenolic compounds. Asian Pac. J Cancer Prev. 2008, 9, 187–196. [Google Scholar] [PubMed]
  108. Bouallagui, Z.; Han, J.; Isoda, H.; Sayadi, S. Hydroxytyrosol rich extract from olive leaves modulates cell cycle progression in MCF-7 human breast cancer cells. Food Chem. Toxicol. 2011, 49, 179–184. [Google Scholar] [CrossRef] [PubMed]
  109. Marrelli, M.; Menichini, F.; Conforti, F. A comparative study of Zingiber officinale Roscoe pulp and peel: Phytochemical composition and evaluation of antitumour activity. Nat. Prod. Res. 2015, 29, 2045–2049. [Google Scholar] [CrossRef] [PubMed]
  110. Hsu, Y.L.; Hung, J.Y.; Tsai, Y.M.; Tsai, E.M.; Huang, M.S.; Hou, M.F.; Kuo, P.L. 6-shogaol, an active constituent of dietary ginger, impairs cancer development and lung metastasis by inhibiting the secretion of CC-chemokine ligand 2 (CCL2) in tumor-associated dendritic cells. J. Agric. Food Chem. 2015, 63, 1730–1738. [Google Scholar] [CrossRef] [PubMed]
  111. Oleaga, C.; Noé, V.; Izquierdo-Pulido, M. Coffee polyphenols change the expression of STAT5B and ATF-2 modifying cyclin D1 levels in cancer cells. Oxid. Med. Cell. Longev. 2012, 2012, 1–17. [Google Scholar] [CrossRef] [PubMed]
  112. Rice-Evans, C.A.; Miller, N.J.; Paganga, G. Structure-antioxidant activity relationships of flavonoids and phenolic acids. Free Radic. Biol. Med. 1996, 20, 933–956. [Google Scholar] [CrossRef]
  113. Kono, Y.; Shibata, H.; Kodama, Y.; Sawa, Y. The suppression of the N-nitrosating reaction by chlorogenic acid. Biochem. J. 1995, 312, 947–953. [Google Scholar] [CrossRef] [PubMed]
  114. Naganuma, T.; Kuriyama, S.; Kakizaki, M.; Sone, T.; Nakaya, N.; Ohmori-Matsuda, K.; Nishino, Y.; Fukao, A.; Tsuji, I. Coffee consumption and the risk of oral, pharyngeal, and esophageal cancers in Japan: The Miyagi Cohort Study. Am. J. Epidemiol. 2008, 168, 1425–1432. [Google Scholar] [CrossRef] [PubMed]
  115. Lewandowska, U.; Fichna, J.; Gorlach, S. Enhancements of anticancer potential of polyphenols by covalent modifications. Biochem. Pharmacol. 2016, 109, 1–13. [Google Scholar] [CrossRef] [PubMed]
Figure 1. The concentration of polyphenols in differnet kinds of oilve oil depending on technological process of the oil extraction [25].
Figure 1. The concentration of polyphenols in differnet kinds of oilve oil depending on technological process of the oil extraction [25].
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Figure 2. Anticancer mechanisms of polyphenols from olive oil [62].
Figure 2. Anticancer mechanisms of polyphenols from olive oil [62].
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Figure 3. Anticancer effects of olive oil polyphenols [115].
Figure 3. Anticancer effects of olive oil polyphenols [115].
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Gorzynik-Debicka, M.; Przychodzen, P.; Cappello, F.; Kuban-Jankowska, A.; Marino Gammazza, A.; Knap, N.; Wozniak, M.; Gorska-Ponikowska, M. Potential Health Benefits of Olive Oil and Plant Polyphenols. Int. J. Mol. Sci. 2018, 19, 686. https://doi.org/10.3390/ijms19030686

AMA Style

Gorzynik-Debicka M, Przychodzen P, Cappello F, Kuban-Jankowska A, Marino Gammazza A, Knap N, Wozniak M, Gorska-Ponikowska M. Potential Health Benefits of Olive Oil and Plant Polyphenols. International Journal of Molecular Sciences. 2018; 19(3):686. https://doi.org/10.3390/ijms19030686

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Gorzynik-Debicka, Monika, Paulina Przychodzen, Francesco Cappello, Alicja Kuban-Jankowska, Antonella Marino Gammazza, Narcyz Knap, Michal Wozniak, and Magdalena Gorska-Ponikowska. 2018. "Potential Health Benefits of Olive Oil and Plant Polyphenols" International Journal of Molecular Sciences 19, no. 3: 686. https://doi.org/10.3390/ijms19030686

APA Style

Gorzynik-Debicka, M., Przychodzen, P., Cappello, F., Kuban-Jankowska, A., Marino Gammazza, A., Knap, N., Wozniak, M., & Gorska-Ponikowska, M. (2018). Potential Health Benefits of Olive Oil and Plant Polyphenols. International Journal of Molecular Sciences, 19(3), 686. https://doi.org/10.3390/ijms19030686

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