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Article

Differential Functional Roles of ALDH1A1 and ALDH1A3 in Mediating Metastatic Behavior and Therapy Resistance of Human Breast Cancer Cells

by
Alysha K. Croker
1,2,
Mauricio Rodriguez-Torres
1,2,
Ying Xia
1,
Siddika Pardhan
3,
Hon Sing Leong
3,
John D. Lewis
4 and
Alison L. Allan
1,5,6,*
1
London Regional Cancer Program, London Health Sciences Centre, 790 Commissioners Road East, London, ON N6A 4L6, Canada
2
Department of Anatomy & Cell Biology, Schulich School of Medicine & Dentistry, Western University, London, ON N6A 5C1, Canada
3
Department of Surgery, Schulich School of Medicine & Dentistry, Western University, London, ON N6A 5C1, Canada
4
Department of Oncology, University of Alberta, 5-142C Katz Group Building, 114th St. and 87th Ave. S., Edmonton, AB T6G 2E1, Canada
5
Department of Oncology and Anatomy & Cell Biology, Schulich School of Medicine & Dentistry, Western University, London, ON N6A 5C1, Canada
6
Cancer Research Laboratory Program, Lawson Health Research Institute, 750 Base Line Road, Suite 300, London, ON N6C 2R5, Canada
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2017, 18(10), 2039; https://doi.org/10.3390/ijms18102039
Submission received: 5 September 2017 / Revised: 18 September 2017 / Accepted: 18 September 2017 / Published: 22 September 2017
(This article belongs to the Special Issue Chemical and Molecular Approach to Tumor Metastases)
Browse Figures
Versions Notes

Abstract

:
Previous studies indicate that breast cancer cells with high aldehyde dehydrogenase (ALDH) activity and CD44 expression (ALDHhiCD44+) contribute to metastasis and therapy resistance, and that ALDH1 correlates with poor outcome in breast cancer patients. The current study hypothesized that ALDH1 functionally contributes to breast cancer metastatic behavior and therapy resistance. Expression of ALDH1A1 or ALDH1A3 was knocked down in MDA-MB-468 and SUM159 human breast cancer cells using siRNA. Resulting impacts on ALDH activity (Aldefluor® assay); metastatic behavior and therapy response in vitro (proliferation/adhesion/migration/colony formation/chemotherapy and radiation) and extravasation/metastasis in vivo (chick choroiallantoic membrane assay) was assessed. Knockdown of ALDH1A3 but not ALDH1A1 in breast cancer cells decreased ALDH activity, and knockdown of ALDH1A1 reduced breast cancer cell metastatic behavior and therapy resistance relative to control (p < 0.05). In contrast, knockdown of ALDH1A3 did not alter proliferation, extravasation, or therapy resistance, but increased adhesion/migration and decreased colony formation/metastasis relative to control (p < 0.05). This is the first study to systematically examine the function of ALDH1 isozymes in individual breast cancer cell behaviors that contribute to metastasis. Our novel results indicate that ALDH1 mediates breast cancer metastatic behavior and therapy resistance, and that different enzyme isoforms within the ALDH1 family differentially impact these cell behaviors.

1. Introduction

Breast cancer is a leading cause of death in women, due primarily to ineffective treatment of metastatic disease. In order to reduce mortality from breast cancer, it is therefore essential to learn more about the metastatic process, and in particular, mechanisms that may contribute to therapy resistance and disease progression [1,2].
Metastasis is a complex process that involves tumor dissemination from the primary tumor to distant sites throughout the body, arrest and extravasation at secondary organ sites, and initiation and maintenance of growth of metastatic lesions [1,3,4]. Given the multi-step nature of this process, it is not surprising that metastasis is highly inefficient, with the main rate-limiting steps being initiation of growth at the secondary site from single tumor cells to micrometastases, and maintenance of that growth into clinically detectable macrometastases [1,3,4,5]. Given the heterogeneous nature of breast cancer, this metastatic inefficiency suggests that only a small subpopulation of tumor cells can successfully navigate the entire metastatic process to successfully form metastases. We have previously identified such a subset of breast cancer cells with high aldehyde dehydrogenase (ALDH) activity and expression of CD44, and demonstrated that these ALDHhiCD44+ cells have enhanced tumor-initiating and metastatic abilities both in vitro and in vivo [6]. Subsequent studies by Charafe-Jauffret et al. (2009, 2010) supported our findings, indicating that ALDHhiCD44+ cells may have a role as metastasis-initiating cells [7,8]. We have also demonstrated that these ALDHhiCD44+ cells are significantly more resistant to chemotherapy and radiation therapy, and that the observed therapy resistance may occur, at least in part, via ALDH-dependent mechanisms [9].
The ALDH superfamily of enzymes is involved in detoxification and/or bioactivation of various intracellular aldehydes in a NAD(P)+-dependent manner [10,11]. Of particular biological importance, the ALDH1 family of enzymes (namely ALDH1A1 and ALDH1A3) plays an important role in oxidizing vitamin A (retinal) to retinoic acid (RA) through an alcohol intermediary. RA functions as a ligand for nuclear retinoid receptors and leads to transactivation and transrepression of target genes, and is finally degraded by CYP26 enzymes [12]. ALDH activity has been shown to be involved in self-protection of normal stem cells and in resistance to the chemotherapeutic drug cyclophosphamide [13]. In the treatment of acute promyelocytic leukemia (APL), the differentiation agent all-trans retinoic acid (ATRA) is used clinically in combination with chemotherapy [14,15]. Increased levels of RA signaling from ATRA treatment have been shown to indirectly suppress ALDH1 promoter activity in liver cells [16], as well as driving the differentiation of promyelocytes into neutrophils, causing enhanced cell-cycle arrest and apoptosis [17]. Additionally, ATRA has been shown to modulate cell growth, apoptosis, and differentiation of breast cancer cells [18]. In terms of therapy resistance, Tanei et al. (2009) conducted a clinical study looking at 108 breast cancer patients who received neoadjuvant paclitaxel and epirubicin-based chemotherapy [19]. When ALDH1A1+ and CD24−CD44+ expression was compared between core needle biopsies (pre-treatment) and subsequent excision (post-treatment), there was a significant increase in ALDH1A1 positive cells, but no change in CD24−CD44+ cells, indicating that ALDH1A1+ cells may play a significant role in resistance to chemotherapy.
High ALDH1 expression has been shown to correlate with poor prognosis in breast cancer patients [20], and has been associated with early relapse, metastasis development, therapy resistance and poor clinical outcome [7,8,21,22,23]. The ALDH1A1 isozyme has been shown to have increased expression in breast cancer patients who present with positive lymph nodes and in patients who succumb to their disease [24]. In a meta-analysis that looked at almost 900 breast cancer cases compared to over 1800 control samples, Zhou et al. (2010) found that ALDH1A1 expression was significantly associated with a high histological grade, ER/PR negativity, HER2 positivity, and worse overall survival [25]. Furthermore, when ALDHbright cells in various tumors, including breast, are treated with ALDH1A1-specific CD8+ T cells which target and eliminate ALDH1A1-positive cells, inhibition of tumorigenic and metastatic growth is observed [26]. In contrast, Marcato et al. (2011) demonstrated that ALDH1A3 (but not ALDH1A1) expression in patient breast tumors correlates significantly with tumor grade, metastasis, and cancer stage, indicating that even within the ALDH1 family, alternate isozymes may function differently [27]. Thus, in addition to the classical role of ALDH as a detoxification enzyme, growing evidence suggests that it may also be playing an additional role in disease progression.
The goal of the current study was to test the hypothesis that ALDH1 is not simply a marker of highly aggressive breast cancer cells and poor patient prognosis, but that it also contributes functionally to metastatic behavior and therapy resistance. Importantly, we wanted to begin to elucidate the differential roles of ALDH1 isozymes, namely ALDH1A1 and ALDH1A3. The novel findings presented here indicate that ALDH1 is functionally involved in breast cancer metastasis and therapy resistance, and that different isozymes within the ALDH1 family differentially impact these cell behaviors.

2. Results

2.1. Treatment with DEAB (Diethylaminobenzaldehyde) Reduces Breast Cancer Cell Proliferation, Adhesion, Migration, and Colony Formation In Vitro

We first investigated whether treating cells with previously established chemical inhibitors of ALDH would have a functional effect on malignant breast cancer cell behavior in vitro, including proliferation, adhesion, migration, and colony formation. This included treatment with a direct competitive substrate of ALDH (diethylaminobenzaldehyde (DEAB)) [28]), as well as the differentiation agent ATRA which has been shown to reduce ALDH promoter activity [9,16]. We observed that cells treated with either ATRA or DEAB demonstrated decreased growth in normal culture relative to respective vehicle control (EtOH) treated cells (p < 0.05) (Figure 1A). MDA-MB-468 cells treated with DEAB were significantly less adherent (Figure 1A) and migratory (Figure 1C) than vehicle control cells, and DEAB-treated SUM159 cells also demonstrated a significant decrease in migration (p < 0.05) (Figure 1C). In contrast, MDA-MB-468 and SUM159 cells treated with ATRA were observed to be significantly more adherent (p < 0.01) (Figure 1B) and migratory (Figure 1C) than respective control cells (p < 0.05). Finally, in keeping with the proliferation results, cells treated with either ATRA or DEAB demonstrated decreased colony formation in soft agar relative to vehicle control cells (p < 0.05) (Figure 1D).

2.2. Decreased Expression of ALDH1A3 but Not ALDH1A1 Reduces ALDH Activity as Measured by the ALDEFLUOR® Assay

Rather than being direct inhibitors of ALDH isozyme expression, DEAB is a competitive substrate of ALDH [28] and ATRA inhibits ALDH promoter activity indirectly through the retinoic acid pathway. In support of this, we did not observe any significant effect of these inhibitors on directly reducing ALDH1A1 or ALDH1A3 protein expression (Figure S1). However, given that previous studies have demonstrated that expression of ALDH1A1 versus ALDH1A3 isozymes have differential correlation with tumor grade, metastasis, and cancer stage in breast cancer patients [27], we wanted to test the hypothesis that directly inhibiting ALDH using the alternative approach of targeted knockdown of ALDH1A1 or ALDH1A3 would also reduce proliferation, adhesion, migration, and colony formation of breast cancer cells.
siRNA was used to knockdown expression of two ALDH1 isozymes (ALDH1A1 and ALDH1A3) in MDA-MB-468 and SUM159 breast cancer cells and generate the following cell populations: 468CON, 468ALDH1A1low, 468ALDH1A3low, 159CON, 159ALDH1A1low, and 159ALDH1A3low. Knockdown of RNA and protein expression was confirmed by quantitative real-time polymerase chain reaction (RT-PCR) and immunoblotting respectively (Figure 2A–C).
There has been some debate over which ALDH1 isozyme is responsible for the ALDH enzymatic activity measured in the ALDEFLUOR® assay. (StemCell Technologies, Vancouver, BC, Canada), with some groups suggesting that ALDH1A1 is responsible, while others believe that it is ALDH1A3 [27,29]. Compared to respective siRNA scrambled controls, we observed that 468ALDH1A3low and 159ALDH1A3low cell populations did demonstrate a significant decrease in ALDH activity (p < 0.001), while 468ALDH1A1low and 159ALDH1A1low cell populations did not exhibit a change in ALDH activity (p > 0.05) (Figure 2D). This data is further supported by the observation that ALDH1A3 mRNA expression is higher than ALDH1A1 mRNA expression in sorted ALDHhi versus unsorted cell populations (Figure S2). Our data also supports previous observations by Marcato et al. (2011), and indicates that the ALDH1A3 isozyme is the major contributor to ALDH activity in breast cancer cells as measured by the ALDEFLUOR® assay [27].

2.3. Decreased Expression of ALDH1A1 Reduces Breast Cancer Cell Proliferation, but Adhesion and Migration of Human Breast Cancer Cells Is Differentially Influenced by ALDH1A1 versus ALDH1A3 In Vitro

Malignant breast cancer cell behavior in vitro was assessed in response to direct knockdown of ALDH1A1 or ALDH1A3 by siRNA (Figure 3). 468ALDH1A1low and 159ALDH1A1low cells demonstrated significantly decreased growth in normal culture relative to respective control cells (p < 0.05), whereas 468ALDH1A3low and 159ALDH1A3low cells showed no difference in proliferation compared to control cells. Lag times (time to reach exponential growth phase) were also observed to be longer for 468ALDH1A1low and 159ALDH1A1low cells versus respective control cells (9 days vs. 5 days for MDA-MB-468 cells; 5 days vs. 3 days for SUM159 cells) (Figure 3A). We next assessed the influence of ALDH1A1 and ALDH1A3 knockdown on breast cancer cell adhesion and migration in vitro (Figure 3B,C). 468ALDH1A1low and 159ALDH1A1low cells were observed to be significantly less adherent (Figure 3B), and less migratory (Figure 3C) than respective control cells (p < 0.05). In contrast, 468ALDH1A3low and 159ALDH1A3low cells were observed to be significantly more adherent and more migratory (Figure 3B,C) than respective control cells (p < 0.05), suggesting that adhesion and migration of human breast cancer cells is differentially influenced by ALDH1A1 versus ALDH1A3. Knockdown of either ALDH1A1 or ALDH1A3 resulted in reduced colony formation in soft agar relative to control cells (p < 0.05) (Figure 3D). It should be noted that the adhesion and migration assays (Figure 3B,C) are performed over time periods of 24 h or less when siRNA knockdown is strong. However, in the proliferation and colony-forming assays (Figure 3A,D), the studies extend well past when the knockdown would be expected to persist. This suggests that the influence of ALDH1 on proliferation and colony formation is an early but important effect that then has a “feed-forward” or downstream effect on the ability of breast cancer cells to proliferate or form established/persistent colonies.

2.4. Decreased Expression of ALDH1A1 and ALDH1A3 Reduces In Vivo Metastatic Ability of Breast Cancer Cells in the Chick Chorioallantoic Membrane (CAM) Assay

In order to assess the metastatic ability of ALDH-deficient cell populations in vivo, GFP-labeled MDA-MB-468 cell populations (468CON, 468ALDH1A1low, 468ALDH1A3low cells) or CMFDA-labeled SUM159 cell populations (159CON, 159ALDH1A1low, 159ALDH1A3low cells) were inoculated on the CAM of 9- or 12-day-old chicken embryos, and the percentage of breast cancer cell extravasation into the CAM and formation of micrometastases in the chicken embryo were analyzed (Figure 4). 468ALDH1A1low and 159ALDH1A1low cells demonstrated a significant decrease in extravasation compared to respective control cells (p < 0.05), whereas there was no significant difference observed in the extravasation of 468ALDH1A3low or 159ALDH1A3low cells compared to control (Figure 4A). In contrast, Both ALDH1A1low and ALDH1A3low cell populations from both MDA-MB-468 and SUM159 cell lines demonstrated a significant decrease in the number of micrometastatic tumors that were able to form compared to control (p < 0.05) (Figure 4B).

2.5. Decreased Expression of ALDH1A1 but Not ALDH1A3 Sensitizes Breast Cancer Cells to Chemotherapy and Radiation In Vitro

Finally, we have previously observed that breast cancer cells with high ALDH activity and CD44 expression (ALDHhiCD44+ phenotype) are significantly more resistant to chemotherapy and radiation therapy, and that this therapy resistance may occur, at least in part, via ALDH1-dependent mechanisms [9]. Taken together with the known role of ALDH activity in cellular self-protection and detoxification [30], we hypothesized that a siRNA-mediated reduction in ALDH1 expression would sensitize MDA-MB-468 and SUM159 cells to chemotherapy and radiation. We observed that knockdown of ALDH1A1 caused a significant sensitization of both MDA-MB-468 and SUM159 cells to paclitaxel (Figure 5A), doxorubicin (Figure 5B), and radiation therapy (Figure 5C) (p < 0.05). In contrast, ALDH1A3 knockdown did not reduce therapy resistance compared to control cells (Figure 5A–C).

3. Discussion

Breast cancer is a leading cause of death in women, primarily due to ineffective treatment of metastatic disease [1,2]. Our group has previously demonstrated that stem-like ALDHhiCD44+ cells play a key role in breast cancer metastasis [6] and are highly resistant to chemotherapy and radiation compared to their ALDHlowCD44− counterparts, potentially as a result of ALDH-dependent mechanisms [9]. Additionally, it has been shown that ALDH1 expression is correlated with early recurrence, worse prognosis, and a higher incidence of metastasis in breast cancer patients [7,20,21,27]. While this suggests that ALDH is an important player in breast cancer metastasis; the actual functional contribution of ALDH1 (in particular its isozymes ALDH1A1 and ALDH1A3) in breast cancer metastasis requires further elucidation, and this was the goal of the current study.
Although the Aldefluor® assay is often used to isolate ALDHhi cancer cells [6,7,8,9,20,31,32], the specific ALDH isozymes that contribute to this activity remain a subject of debate. In this assay, cells are incubated in a buffer containing a fluorescent aldehyde substrate (bodipy-aminoacetylaldehyde). The aminoacetylaldehyde is taken up into the cells via passive diffusion. Once inside the cell, intracellular ALDH oxidizes the aminoacetylaldehyde into aminoacetate, which is negatively charged, and therefore retained inside the cell, causing the cells to fluoresce [32]. When ALDH1A1 was knocked down in both MDA-MB-468 and SUM159 cell lines, there was no observable change in ALDH activity as measured by the Aldefluor® assay; however, when ALDH1A3 was knocked down, there was an approximate 50% reduction in ALDH activity measured by the Aldefluor® assay. This is consistent with breast cancer studies done by Marcato et al. (2011), who observed that ALDH1A3 knockdown was better correlated with a decrease in Aldefluor® activity compared to ALDH1A1 and ALDH2 [27]. Additional studies have reported that ALDH1A1, ALDH7A1, ALDH2 and/or ALDH1A2 are responsible for driving Aldefluor® activity in other tumor types [32,33,34], indicating that the ALDH isoform(s) responsible for Aldefluor® activity may be tumor-specific. Furthermore, in the present study, even after ALDH1A3 knockdown, there was still approximately 50% normal ALDH activity, indicating that other ALDH isozymes might be involved in the context of breast cancer. Taken together, these results suggest that many ALDH isozymes may contribute to the ALDH activity measured by the Aldefluor® assay, and potentially that different isozymes may contribute to ALDH activity in different tumor types.
We previously reported that ALDHhiCD44+ cells demonstrated enhanced proliferation, adhesion, and migration [6]. Additional work in lung and liver cancer cells has suggested that a decrease in ALDH expression can result in a decrease in proliferation [35,36,37]. In the current study, we treated breast cancer cells with DEAB (a direct competitive substrate of ALDH [28]) and observed a decrease in cell proliferation, as well as in adhesion and migration in vitro compared to control cells, suggesting that ALDH may potentially contribute to these processes. In order to determine whether ALDH1 isozymes were also involved in these processes, we used siRNA to specifically knockdown ALDH1A1 or ALDH1A3 and observed that ALDH1A1low cells demonstrated decreased proliferation, adhesion, and migration in vitro. In contrast, cells in which ALDH1A3 had been knocked down showed no change in proliferation and in fact demonstrated increased levels of adhesion and migration in vitro.
ALDH1 expression has been clinically correlated with an increased incidence of metastasis [7,20,27]. We used the chick CAM assay to elucidate whether ALDH1A1 and/or ALDH1A3 functionally contributed to metastasis. Cells with decreased ALDH1A1 expression demonstrated decreased abilities to invade/extravasate; whereas cells with decreased ALDH1A3 expression demonstrated no change in invasive capabilities compared to control cells in vivo. However, in terms of the actual formation of metastases in vivo; both ALDH1A1low and ALDH1A3low cells demonstrated a decrease in metastatic potential, with an approximate 50% reduction in the number of micrometastases that were able to form in the chick CAM compared to control cells.
Finally, we have previously observed that that ALDHhiCD44+ cells demonstrate high levels of therapy resistance, and that pre-treatment targeting of ALDH activity using DEAB or ATRA can sensitize these resistant cells to both anthracycline and taxane chemotherapy, as well as radiation [9]. In the current study, we directly targeted specific ALDH1 isozymes using siRNA and tested the effect on therapy response. Notably, when ALDH1A1 expression was decreased, there was a significant sensitization of the cancer cells to both chemotherapy and radiation. Cells with decreased ALDH1A3 expression, however, showed no change in therapy resistance to either chemotherapy or radiation. These results suggest that the ALDH1A1 isozyme is an important contributor to therapy resistance in breast cancer cells, not only to cyclophosphamide chemotherapy (as previously reported [13,38]), but also to other classes of chemotherapy and radiotherapy.
Our study is the first in the literature to systematically examine the functional roles of ALDH1 isozymes on individual breast cancer cell behaviors that collectively contribute to the metastatic process. The combined in vitro and in vivo data presented in this study suggests that ALDH1A1 and ALDH1A3 both contribute functionally to various steps in the breast cancer metastatic cascade; however, they may do so in different ways (summarized in Table 1). For example, it appears that ALDH1A1 may mediate the adhesion, migration, extravasation, and initial colonization steps; whereas ALDH1A3 may only participate in colonization and sustainment of metastatic growth. This data both supports and contradicts previous work by Marcato et al. (2011), who reported that ALDH1A3 and not ALDH1A1 correlated with metastatic disease in breast cancer patients [27]. More recent work by this group led to the observation that overexpression of ALDH1A3 in MDA-MB-231 human breast cancer cells increases in vitro invasion and in vivo primary tumor growth and lung metastasis in mice, likely due to changes in RA signaling [39]. Although they observed that knockdown of either ALDH1A1 or ALDH1A3 in MDA-MB-231 cells did not have an effect on malignant behavior, this was not surprising given that this cell line has very low levels of these isozymes to begin with [27]. In contrast, it was somewhat surprising that their knockdown of ALDH1A1 in MDA-MB-468 cells (one of the cell lines used in the present study) actually increased primary tumor growth in mice, which is somewhat in contrast with our observed reduction in proliferation, colony-formation, and in vivo metastasis data presented in the current study. Overall, Marcato et al. [39] observed cell line-specific differences with regards to ALDH1A3 function in malignancy and metastasis. In contrast, our data shows that knockdown of ALDH1A1 consistently reduces most steps in the metastatic cascade except for basic proliferation in two different human breast cancer cell lines with different genetic backgrounds and differing metastatic ability. These experimental findings are supported by clinical data, which demonstrates that ALDH1A1 expression is often associated with worse prognosis in breast and other cancers [7,20,24,40,41,42,43].
Overall, the results of this study support the concept that ALDH1 plays a functional role in both breast cancer metastasis and therapy resistance; although the ALDH1A1 and ALDH1A3 isozymes seemed to contribute to these behaviors in different ways. In order to determine the underlying reasons for the differential influence of ALDH1 on different malignant behaviors, in-depth mechanistic studies will need to be carried out in the future. In addition, the observation that ALDH1A3 knockdown only caused a 50% reduction in ALDH activity suggests that other ALDH isozymes must be involved in Aldefluor® activity in breast cancer cells. It would therefore be interesting in the future to determine the functional role of other ALDH isozymes in breast cancer metastasis (i.e., ALDH7A1, ALDH1A2, and/or ALDH2) [33], as well as to assess corresponding changes in genes, transcription factors, and epigenetic modifiers that may ultimately be driving the process of metastasis. Elucidation of the mechanisms by which ALDH1A1, ALDH1A3 and other ALDH isozymes contribute to disease progression could have potentially important implications for the management and treatment of breast cancer in the future. Furthermore, additional investigation of ALDH1A1-specific therapy resistance mechanisms is required, and translating this knowledge into the clinic through development of either a direct, specific ALDH1A1 inhibitor or an ALDH1A1-related inhibitor that is safe for human use could have important implications for the management of both primary and metastatic breast cancer. Finally, it is well known that treating breast cancer before metastasis is observed (i.e., in the adjuvant setting) is significantly correlated with better patient survival [6,9,44]. Given that ALDH1 has been both correlated with metastatic disease and shown to functionally contribute to metastasis, it may be beneficial to use assessment of ALDH1 expression in the primary tumor as a clinical tool for identifying breast cancer patients with a high risk of metastasis and stratifying them for aggressive therapy to prevent disease recurrence or progression.

4. Materials and Methods

4.1. Cell Culture, Reagents, and Therapy Conditions

MDA-MB-468 cells were a kind gift from Dr. Janet Price, M.D. Anderson Cancer Center, (Houston, TX, USA) [45], and were maintained in αMEM +10% fetal bovine serum (FBS). The 468 subline expressing green fluorescent protein (GFP) was generated previously as described [46]. SUM159 cells [47] were obtained from Asterand (Detriot, MI, USA) and maintained in Hams: F12 + 5% FBS. CellTracker™ 5-chloromethylfluorescein diacetate (CMFDA; Invitrogen, Carlsbad, CA, USA) was used to label SUM159 cells for the CAM assay. All cell lines were authenticated via third party testing of 9 short tandem repeat (STR) loci on 11 April 2103. (CellCheck, RADIL, Columbia, MO, USA). All media was obtained from Invitrogen. FBS was obtained from Sigma (St. Louis, MO, USA). Tissue culture plastic was obtained from NUNC (Roskilde, Denmark).
All-trans retinoic acid (ATRA) and diethylamino-benzaldehyde DEAB (Sigma) were constituted in 100% ethanol and diluted in either Hams:F12 (SUM159 cells) or α-MEM (MDA-MB-468 cells) at 5 μM (ATRA) or 100 μM (DEAB). Doxorubicin (Novopharm Limited, Toronto, ON, Canada) and paclitaxel (Biolyse Pharma Corporation, St. Catherines, ON, Canada) were diluted in either Hams: F12 or α-MEM to the concentrations noted below. Radiation was administered at the doses noted below using a Cobalt-60 irradiator (Theratron 60, Atomic Energy of Canada Limited, Chalk River, ON, Canada). All treatment doses were selected based on LC50 values determined in previous experiments [9].

4.2. Cell Proliferation Assays

Breast cancer cells were counted and plated at a density of 5.0 × 104 cells/60 mm plate (n = 3 per time point) and maintained in regular growth media. Every 48 h for 14 days, cultures (n = 3) were trypsinized and counted using a hemocytometer. Doubling time of each cell population was estimated during the exponential growth phase according to Td = 0.693t/ln (Nt/N0), where t is time (in hours), Nt is the cell number at time t, and N0 is the cell number at initial time.

4.3. Cell Adhesion Assays

Breast cancer cells were plated onto sterile 96-well non-tissue culture plates (Titertek, Flow Laboratories Inc.; McLean, VA, USA) that had been treated with one of: 20 μg/mL of human laminin (Sigma; SUM159 cells), 5 μg/mL of human vitronectin (Sigma; MDA-MB-468 cells), or PBS (negative control), using 1 × 104 cells/well (n = 3) for each cell population. Laminin and vitronectin were chosen based on previous experiments in our laboratory that have demonstrated that SUM159 and MDA-MB-468 cells differentially express integrin receptors for vitronectin and laminin respectively [48,49]. Cells were allowed to adhere for 5 h, after which non-adhered cells were rinsed away. Adhered cells were fixed with 2% gluteraldehyde and stained using Harris’ hematoxylin. Five high powered fields (HPF) (200×) were counted for each well, and mean numbers of adhered cells/field were calculated and normalized to control cell populations.

4.4. Cell Migration Assays

Transwell plates (8 μm pore size, 6.5 mm; Becton Dickinson; Franklin Lakes, NJ, USA) were coated with 6 μg/well of gelatin (Sigma) [50,51]. Chemoattractant (5% FBS) or control (0.01% BSA) media was placed in the bottom portion of each well. For each cell population, 5 × 104 cells were plated on top of the transwells. After 24 h, the upper transwell was removed, inverted, fixed with 1% gluteraldehyde, and stained with Harris’ hematoxylin. A cotton swab was used to carefully remove non-migrated cells on the inner surface of the transwell. For each well, five HPF were counted and mean numbers of migrated cells/field were calculated and normalized to control cell populations.

4.5. Colony Forming Assays

Dishes (60 mm) were coated with 1% agarose (Bioshop; Burlington, ON, Canada) in normal growth media and allowed to solidify for 1 hr. Breast cancer cell suspensions (1.0 × 104 cells/60 mm plate) were prepared using 0.6% agarose in normal growth media and plated on top of the base agarose base layer (n = 4 for each time point). Normal growth media was added on top of the cell layer and changed every 3–4 days for 4 weeks, after which the media was removed and plates were fixed in 10% neutral-buffered formalin (EM Sciences, Gladstone, NJ, USA). For each dish, 5 HPF were counted and mean number of colonies per field were calculated and normalized to control cell populations.

4.6. siRNA Knockdown of ALDH1A1 and ALDH1A3

ON-TARGET plus SMART pool small interfering RNAs (siRNA) (Dharmacon Thermo Scientific, Lafayette, CO, USA) were used to transiently transfect human ALDH1A1 and ALDH1A3 into MDA-MB-468 and SUM149 cells. All siRNAs were suspended in sterile RNAse-free water at a concentration of 25 μM. Scrambled control (20–50 μL/mL), ALDH1A1 (20 μL/mL), ALDH1A3 (50 μL/mL) siRNAs and Lipofectamine RNAiMax reagent (20 μL/mL; Invitrogen) were diluted into serum-free Opti-MEM (Invitrogen). Lipofectamine and siRNA concentrations were determined based on preliminary experiments which indicated the greatest knockdown of the proteins of interest [49]. The transfections yielded the following cell populations used in further experiments: 468CON, 468ALDH1A1low, 468ALDH1A3low, 159CON, 159ALDH1A1low, and 159ALDH1A3low.

4.7. RNA Isolation and Quantitative RT-PCR

Total RNA was extracted using TRIzol (Invitrogen) according to the manufacturer’s protocol. Total RNA was reverse transcribed using Superscript III (Invitrogen) and the Eppendorf Mastercycler Gradient (Eppendorf, Hamburg, Germany). Primers and cycling conditions used for ALDH1A1, ALDH1A3, and GAPDH are provided in Table 2. Relative quantification of ALDH1A1 and ALDH1A3 gene expression in MDA-MB-468 and SUM159 breast cancer cells was determined by quantitative PCR using Brilliant® II SYBR® Green qPCR Low ROX Master Mix (Agilent Technologies, Eugene, OR, USA) and the delta Ct method. GAPDH was used for normalization.

4.8. Immunoblotting

Cell lysates were extracted and protein (10 μg) was subjected to sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE, 12%) and transferred onto polyvinylidene difluoride membranes (PVDF; Immobilon™, Millipore; Bedford, MA, USA). Blocking and antibody dilution was done using 5% skim milk in Tris-buffered saline with 0.1% Tween-20 (TBST). Anti-human primary antibodies included mouse monoclonal ALDH1A1 (clone IG6; 1:1000) and rabbit polyclonal ALDH1A3 (1:500) (Abcam, Cambridge, MA, USA). Secondary antibodies included goat anti-mouse and mouse anti-rabbit antibodies conjugated to horseradish peroxidase (Calbiochem, Gibbstown, NJ, USA) (1:2000). Protein expression was visualized using Amersham ECL Plus (GE Healthcare, Baie d’Urfe, QC, Canada) using β-actin (Sigma, 1:5000) as a loading control.

4.9. ALDEFLUOR® Assay

The ALDEFLUOR® assay (StemCell Technologies, Vancouver, BC, Canada) was used to assess ALDH activity as described previously [52,53,54]. Briefly, cells were harvested, placed in ALDEFLUOR® assay buffer (2 × 106/mL), and incubated with ALDEFLUOR® substrate for 45 min at 37 °C to allow substrate conversion. As a negative control for all experiments, an aliquot of ALDEFLUOR®-stained cells was immediately quenched with 1.5-mM diethylaminobenzaldehyde (DEAB), a specific ALDH inhibitor. Cells were analyzed using the green fluorescence channel (FL1) on a Beckman Coulter EPICS XL-MCL flow cytometer.

4.10. Chick Embryo Chorioallantoic Membrane (CAM) Assay

For assessment of in vivo extravasation and metastasis, chick embryo chorioallantoic membrane (CAM) assays were used as described previously [55,56]. Briefly, fertilized chicken eggs (McKinley Hatchery, St. Mary’s, ON, Canada) were removed from their shell, placed in covered dishes, and maintained ex ovo at 37 °C with 90% humidity. Embryos were used at day 9 (micrometastasis assay) and day 12 (extravasation assay). Green-fluorescent protein (GFP) labeled MDA-MB-468 or CellTracker™ CMFDA-labeled SUM159 cell populations were injected intravenously (i.v.) into the CAM as described previously [55,56] using 1 × 105 (extravasation assay) or 2 × 105 (micrometastasis assay) cells/egg (n = 8–17 eggs per treatment group). For the extravasation assay, a portion of the CAM was sectioned off using aluminum foil and the number of cells arrested in the sectioned-off area was manually counted using a fluorescence microscope at 20× magnification. Embryos were then returned to the incubator for 24 h, after which time the number of extravasated cells in the sectioned off area were manually counted using a fluorescence microscope. Percent extravasation was calculated by dividing the number of initial cells by the number of successfully extravasated cells in the CAM. For the micrometastasis assay, embryos were returned to the incubator for 7 days after cell injection to allow the formation of metastases. After 7 days, the number of micrometastatic tumors that developed following the i.v. injection were manually counted using a fluorescence microscope at 4× magnification.

4.11. Chemotherapy and Radiation Treatment

Cell populations were plated at a density of 5 × 105 cells in 6-well plates (n = 3/treatment group) and maintained in normal growth medium for 24 h. Cells were then treated with either normal media alone (control), chemotherapy (paclitaxel (0.2 μM); doxorubicin (0.4 μM)), or radiation (2 × 5Gy, MDA-MB-468; or 2 × 15Gy, SUM159) and cultured for a further 72 h. Cells were then harvested and viable cells were quantified using trypan blue exclusion and manual counting on a hemocytometer using light microscopy.

4.12. Statistical Analysis

All experiments were performed following at least three separate siRNA transfections with at least 3 biological replicates included within each experiment. In all cases, quantitative data was compiled from all experiments. Statistical analysis was performed using GraphPad Prism 4.0 software© (San Diego, CA, USA) using either t-test (for comparison between 2 groups) or analysis of variance (ANOVA) with Tukey post-test (for comparison between more than 2 groups) when groups passed both a normality test and an equal variance test. When this was not the case, the Mann-Whitney Rank-Sum test was used. Unless otherwise noted, data is presented as the mean ± SEM. In all cases, p values of ≤0.05 were regarded as being statistically significant.

Supplementary Materials

Supplementary materials can be found at www.mdpi.com/1422-0067/18/10/2039/s1.

Acknowledgments

This work was supported by grants from the Canadian Breast Cancer Foundation-Ontario Region and the Canada Foundation for Innovation (#13199). The work was also supported by the Breast Cancer Society of Canada (Alysha K. Croker, Mauricio Rodriguez-Torres, and Alison L. Allan) and by donor support from John and Donna Bristol through the London Health Sciences Foundation (Alison L. Allan). Alysha K. Croker was the recipient of a Canadian Institute of Health Research (CIHR) Banting & Best Doctoral Scholarship. Mauricio Rodriguez-Torres was the recipient of a Vanier Canada Graduate Scholarship. Alison L. Allan was supported by a CIHR New Investigator Award and an Early Researcher Award from the Ontario Ministry of Research and Innovation.

Author Contributions

Alysha K. Croker and Alison L. Allan conceived and designed the experiments; Alysha K. Croker, Mauricio Rodriguez-Torres, Ying Xia, Siddika Pardhan, and Hon Sing Leong performed the experiments; Alysha K. Croker, Mauricio Rodriguez-Torres, Ying Xia and Alison L. Allan analyzed the data; John D. Lewis and Alison L. Allan contributed reagents/materials/analysis tools; and Alysha K. Croker and Alison L. Allan wrote the paper.

Conflicts of Interest

The authors declare no conflict of interest. The funding sponsors had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, and in the decision to publish the results.

Abbreviations

ALDHAldehyde dehydrogenase
ANOVAAnalysis of variance
APLAcute promyelocytic leukemia
ATRAAll-trans retinoic acid
BSABovine serum albumin
CAMChoroiallantoic membrane assay
CDCluster of differentiation
CMFDA5-chloromethylfluorescein diacetate
CYPCytochrome P450
DEABDiethylaminobenzaldehyde
ECLEnhanced chemiluminescence
EREstrogen receptor
EtOHEthanol
FBSFetal bovine serum
GAPDHGlyceraldehyde 3-phosphate dehydrogenase
GFPGreen fluorescent protein
GyGray
HPFHigh-powered field
LC50Lethal concentration (50%)
NAD(P)Nicotinamide adenine dinucleotide phosphate
PBSPhosphate buffered saline
PCRPolymerase chain reaction
PRProgesterone receptor
PVDFPolyvinylidene fluoride
RARetinoic acid
RTReverse transcriptase
SDS-PAGESodium dodecyl sulfate polyacrylamide gel electrophoresis
SEMStandard error of the mean
siRNASmall interfering RNA
STRShort tandem repeat
TBSTTris-buffered saline + Tween-20

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Figure 1. Treatment with diethylaminobenzaldehyde (DEAB) reduces breast cancer cell (A) proliferation, (B) adhesion, (C) migration, and (D) colony formation in vitro. MDA-MB-468 (left panels) and SUM159 (right panels) human breast cancer cells were treated with 5 μM all-trans retinoic acid (ATRA), 100 μM DEAB or ethanol (EtOH) as a vehicle control (CON). In all cases, data represents the mean ± standard error of the mean (SEM) normalized to vehicle control. * = significantly different than respective vehicle control treatment (p < 0.05).
Figure 1. Treatment with diethylaminobenzaldehyde (DEAB) reduces breast cancer cell (A) proliferation, (B) adhesion, (C) migration, and (D) colony formation in vitro. MDA-MB-468 (left panels) and SUM159 (right panels) human breast cancer cells were treated with 5 μM all-trans retinoic acid (ATRA), 100 μM DEAB or ethanol (EtOH) as a vehicle control (CON). In all cases, data represents the mean ± standard error of the mean (SEM) normalized to vehicle control. * = significantly different than respective vehicle control treatment (p < 0.05).
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Figure 2. Decreased expression of ALDH1A3 but not ALDH1A1 reduces ALDH activity as measured by the Aldefluor® assay. MDA-MB-468 (left panels) or SUM159 (right panels) human breast cancer cells were transfected with 100 pmol siRNA pool targeted towards ALDH1A1, ALDH1A3, or a scrambled control using Lipofectamine to generate the following cell lines: 468CON, 468ALDH1A1low, 468ALDH1A3low, 159CON, 159ALDH1A1low, and 159ALDH1A3low. After 4 days, RNA, cell lysates, or cells were collected and (A,B) qRT-PCR, (C) immunoblotting, or (D) Aldefluor® assays were performed to assess ALDH1 gene expression, ALDH1 protein expression, and ALDH enzyme activity (respectively). Data represents the mean ± SEM. * = significantly different than respective siCON, 468CON, or 159CON scrambled control cells (p < 0.05).
Figure 2. Decreased expression of ALDH1A3 but not ALDH1A1 reduces ALDH activity as measured by the Aldefluor® assay. MDA-MB-468 (left panels) or SUM159 (right panels) human breast cancer cells were transfected with 100 pmol siRNA pool targeted towards ALDH1A1, ALDH1A3, or a scrambled control using Lipofectamine to generate the following cell lines: 468CON, 468ALDH1A1low, 468ALDH1A3low, 159CON, 159ALDH1A1low, and 159ALDH1A3low. After 4 days, RNA, cell lysates, or cells were collected and (A,B) qRT-PCR, (C) immunoblotting, or (D) Aldefluor® assays were performed to assess ALDH1 gene expression, ALDH1 protein expression, and ALDH enzyme activity (respectively). Data represents the mean ± SEM. * = significantly different than respective siCON, 468CON, or 159CON scrambled control cells (p < 0.05).
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Figure 3. Decreased expression of ALDH1A1 reduces breast cancer cell proliferation, but adhesion and migration of human breast cancer cells is differentially influenced by ALDH1A1 versus ALDH1A3 in vitro. MDA-MB-468 (left panels) and SUM159 (right panels) human breast cancer cells were treated with control siRNA (siCON) or ALDH-specific siRNA (siALDH1A1 or siALDH1A3) for 96 h to generate the following cell lines: 468CON, 468ALDH1A1low, 468ALDH1A3low, 159CON, 159ALDH1A1low, 159ALDH1A3low. (A) Proliferation; (B) adhesion assays; (C) migration; and (D) colony formation. In all cases, data represents the mean ± SEM normalized to respective scrambled control. * = significantly different than respective scrambled control (p < 0.05).
Figure 3. Decreased expression of ALDH1A1 reduces breast cancer cell proliferation, but adhesion and migration of human breast cancer cells is differentially influenced by ALDH1A1 versus ALDH1A3 in vitro. MDA-MB-468 (left panels) and SUM159 (right panels) human breast cancer cells were treated with control siRNA (siCON) or ALDH-specific siRNA (siALDH1A1 or siALDH1A3) for 96 h to generate the following cell lines: 468CON, 468ALDH1A1low, 468ALDH1A3low, 159CON, 159ALDH1A1low, 159ALDH1A3low. (A) Proliferation; (B) adhesion assays; (C) migration; and (D) colony formation. In all cases, data represents the mean ± SEM normalized to respective scrambled control. * = significantly different than respective scrambled control (p < 0.05).
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Figure 4. Decreased expression of ALDH1A1 and ALDH1A3 reduces in vivo metastatic ability of breast cancer cells in the chick CAM assay. GFP-labeled MDA-MB-468 or CMFDA-labeled SUM159 cell populations were transfected with 100 pmol (MDA-MB-468) or 400 pmol (SUM159) siRNA targeted towards ALDH1A1, ALDH1A3, or scrambled control using Lipofectamine to generate the following cell lines: 468CON, 468ALDH1A1low, 468ALDH1A3low, 159CON, 159ALDH1A1low, 159ALDH1A3low. After 4 days, 1 × 105 (extravasation assay) or 2 × 105 (micrometastasis assay) cells were injected into chicken embryos and (A) cell extravasation was observed after 24 h, or (B) micrometastatic formation was observed after 7days. Data represents the mean ± SEM normalized to control cells. * = significantly different than respective 468CON and 159CON cells (p < 0.05).
Figure 4. Decreased expression of ALDH1A1 and ALDH1A3 reduces in vivo metastatic ability of breast cancer cells in the chick CAM assay. GFP-labeled MDA-MB-468 or CMFDA-labeled SUM159 cell populations were transfected with 100 pmol (MDA-MB-468) or 400 pmol (SUM159) siRNA targeted towards ALDH1A1, ALDH1A3, or scrambled control using Lipofectamine to generate the following cell lines: 468CON, 468ALDH1A1low, 468ALDH1A3low, 159CON, 159ALDH1A1low, 159ALDH1A3low. After 4 days, 1 × 105 (extravasation assay) or 2 × 105 (micrometastasis assay) cells were injected into chicken embryos and (A) cell extravasation was observed after 24 h, or (B) micrometastatic formation was observed after 7days. Data represents the mean ± SEM normalized to control cells. * = significantly different than respective 468CON and 159CON cells (p < 0.05).
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Figure 5. Decreased expression of ALDH1A1 but not ALDH1A3 sensitizes breast cancer cells to chemotherapy and radiation. MDA-MB-468 cells (left panels) and SUM159 cells (right panels) were treated with control siRNA (siCON) or ALDH-specific siRNA (ALDH1A1 or ALDH1A3) for 96 h to generate the following cell lines: 468CON, 468ALDH1A1low, 468ALDH1A3low, 159CON, 159ALDH1A1low, 159ALDH1A3low. Cell populations were treated with (A) paclitaxel (0.2 μg/mL), (B) doxorubicin (0.2 μg/mL), or (C) radiation (2 × 5Gy; MDA-MB-468 or 2 × 15Gy; SUM159). Data represents the mean ± SEM normalized to respective control cells. * = significantly different than respective 468CON or 159CON cells treated with paclitaxel, doxorubicin, or radiation (p < 0.01).
Figure 5. Decreased expression of ALDH1A1 but not ALDH1A3 sensitizes breast cancer cells to chemotherapy and radiation. MDA-MB-468 cells (left panels) and SUM159 cells (right panels) were treated with control siRNA (siCON) or ALDH-specific siRNA (ALDH1A1 or ALDH1A3) for 96 h to generate the following cell lines: 468CON, 468ALDH1A1low, 468ALDH1A3low, 159CON, 159ALDH1A1low, 159ALDH1A3low. Cell populations were treated with (A) paclitaxel (0.2 μg/mL), (B) doxorubicin (0.2 μg/mL), or (C) radiation (2 × 5Gy; MDA-MB-468 or 2 × 15Gy; SUM159). Data represents the mean ± SEM normalized to respective control cells. * = significantly different than respective 468CON or 159CON cells treated with paclitaxel, doxorubicin, or radiation (p < 0.01).
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Table
Table 1. Summary of functional consequences of ALDH1A1 and ALDH1A3 knockdown in MDA-MB-468 and SUM159 human breast cancer cells.
Table 1. Summary of functional consequences of ALDH1A1 and ALDH1A3 knockdown in MDA-MB-468 and SUM159 human breast cancer cells.
Functional Behavior/ActivityALDH1A1 KnockdownALDH1A3 Knockdown
ALDH Activity (Aldeflour)No effect ↓
Proliferation ↓ No effect
Adhesion ↓ ↑
Migration ↓ ↑
Colony Formation ↓ ↓
Extravasation ↓ No effect
Metastasis ↓ ↓
Therapy Resistance ↓ No effect
↑ = increase in respective functional behavior/activity; ↓ = decrease in respective functional behavior/activity.
Table
Table 2. Primers and qPCR conditions.
Table 2. Primers and qPCR conditions.
GenePrimer SequenceqPCR Cycling ConditionsNumber of CyclesProduct Size (bp)
ALDH1A1Fwd: 5′-CGT TGG TTA TGC TCA TTT GGA A-3′
Rev: 5′-TGA TCA ACT TGC CAA CCT CTG T-3′		60 s 55 °C
60 s 72 °C
60 s 95 °C		4522 bp
ALDH1A3Fwd: 5′-ATG TGG GAA AAC CCC CTG TG-3′
Rev: 5′-GAA TGG TCC CAC CTT CAC CT-3′		60 s 57 °C
60 s 72 °C
60 s 95 °C		4520 bp
GAPDHFwd: 5′-CAT GTT CGT CAT GGG TGT GAA CCA-3′
Rev: 5′-ATG GCA TGG ACT GTG GTC ATG AGT -3′		45 s 60 °C
45 s 72 °C
60 s 95 °C		4024 bp

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MDPI and ACS Style

Croker, A.K.; Rodriguez-Torres, M.; Xia, Y.; Pardhan, S.; Leong, H.S.; Lewis, J.D.; Allan, A.L. Differential Functional Roles of ALDH1A1 and ALDH1A3 in Mediating Metastatic Behavior and Therapy Resistance of Human Breast Cancer Cells. Int. J. Mol. Sci. 2017, 18, 2039. https://doi.org/10.3390/ijms18102039

AMA Style

Croker AK, Rodriguez-Torres M, Xia Y, Pardhan S, Leong HS, Lewis JD, Allan AL. Differential Functional Roles of ALDH1A1 and ALDH1A3 in Mediating Metastatic Behavior and Therapy Resistance of Human Breast Cancer Cells. International Journal of Molecular Sciences. 2017; 18(10):2039. https://doi.org/10.3390/ijms18102039

Chicago/Turabian Style

Croker, Alysha K., Mauricio Rodriguez-Torres, Ying Xia, Siddika Pardhan, Hon Sing Leong, John D. Lewis, and Alison L. Allan. 2017. "Differential Functional Roles of ALDH1A1 and ALDH1A3 in Mediating Metastatic Behavior and Therapy Resistance of Human Breast Cancer Cells" International Journal of Molecular Sciences 18, no. 10: 2039. https://doi.org/10.3390/ijms18102039

APA Style

Croker, A. K., Rodriguez-Torres, M., Xia, Y., Pardhan, S., Leong, H. S., Lewis, J. D., & Allan, A. L. (2017). Differential Functional Roles of ALDH1A1 and ALDH1A3 in Mediating Metastatic Behavior and Therapy Resistance of Human Breast Cancer Cells. International Journal of Molecular Sciences, 18(10), 2039. https://doi.org/10.3390/ijms18102039

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