Curcumin inhibits breast cancer stem cell migration by amplifying the E-cadherin/β-catenin negative feedback loop
© Mukherjee et al.; licensee BioMed Central Ltd. 2014
Received: 12 April 2014
Accepted: 6 October 2014
Published: 14 October 2014
The existence of cancer stem cells (CSCs) has been associated with tumor initiation, therapy resistance, tumor relapse, angiogenesis, and metastasis. Curcumin, a plant ployphenol, has several anti-tumor effects and has been shown to target CSCs. Here, we aimed at evaluating (i) the mechanisms underlying the aggravated migration potential of breast CSCs (bCSCs) and (ii) the effects of curcumin in modulating the same.
The migratory behavior of MCF-7 bCSCs was assessed by using cell adhesion, spreading, transwell migration, and three-dimensional invasion assays. Stem cell characteristics were studied by using flow cytometry. The effects of curcumin on bCSCs were deciphered by cell viability assay, Western blotting, confocal microscopy, and small interfering RNA (siRNA)-mediated gene silencing. Evaluations of samples of patients with breast cancer were performed by using immunohistochemistry and flow cytometry.
Here, we report that bCSCs are endowed with aggravated migration property due to the inherent suppression of the tumor suppressor, E-cadherin, which is restored by curcumin. A search for the underlying mechanism revealed that, in bCSCs, higher nuclear translocation of beta-catenin (i) decreases E-cadherin/beta-catenin complex formation and membrane retention of beta-catenin, (ii) upregulates the expression of its epithelial-mesenchymal transition (EMT)-promoting target genes (including Slug), and thereby (iii) downregulates E-cadherin transcription to subsequently promote EMT and migration of these bCSCs. In contrast, curcumin inhibits beta-catenin nuclear translocation, thus impeding trans-activation of Slug. As a consequence, E-cadherin expression is restored, thereby increasing E-cadherin/beta-catenin complex formation and cytosolic retention of more beta-catenin to finally suppress EMT and migration of bCSCs.
Cumulatively, our findings disclose that curcumin inhibits bCSC migration by amplifying E-cadherin/beta-catenin negative feedback loop.
Breast cancer is the most common form of cancer diagnosed in women. In 2013, breast cancer accounted for 29% of all new cancer cases and 14% of all cancer deaths among women worldwide. Breast cancer-related mortality is associated with the development of metastatic potential of the primary tumor. Given this high rate of incidence and mortality, it is critical to understand the mechanisms behind metastasis and identify new targets for therapy. For the last few decades, various modalities of cancer therapy were being investigated. But the disease has remained unconquered, largely because of its invasive nature.
Amidst the research efforts to better understand cancer progression, there has been increasing evidence that hints at a role for a subpopulation of tumorigenic cancer cells, termed cancer stem cells (CSCs), in metastasis formation. CSCs are characterized by their preferential ability to initiate and propagate tumor growth and their selective capacity for self-renewal and differentiation into less tumorigenic cancer cells. There are reports which demonstrate that CSCs are enriched among circulating tumor cells in the peripheral blood of patients with breast cancer. Moreover, recent studies show that epithelial-mesenchymal transition (EMT), an early step of tumor cell migration, can induce differentiated cancer cells into a CSC-like state. These observations have established a functional link between CSCs and EMT and suggest that CSCs may underlie local and distant metastases by acquiring mesenchymal features which would greatly facilitate systemic dissemination from the primary tumor mass. Taken together, these studies suggest that CSCs may be a critical factor in the metastatic cascade. Now, the incurability of the malignancy of the disease raises the question of whether conventional anti-cancer therapies target the correct cells since the actual culprits appear to be evasive of current treatment modalities.
Studies focusing on the early steps in the metastatic cascade, such as EMT and altered cell adhesion and motility, have demonstrated that aggressive cancer progression is correlated with the loss of epithelial characteristics and the gain of migratory and mesenchymal phenotype, for which downregulation of E-cadherin is a fundamental event. A transcriptional consequence of the presence of E-cadherin in epithelial cells can be inferred from the normal association of E-cadherin with β-catenin in adherens junctions. This association prevents β-catenin transfer to the nucleus and impedes its role as a transcriptional activator, which occurs through its interaction mainly with the TCF (T-cell factor)-LEF (lymphoid enhancer factor) family of transcription factors but also with other DNA-binding proteins. Accordingly, the involvement of β-catenin signaling in EMTs during tumor invasion has been established. Aberrant expression of β-catenin has been reported to induce malignant pathways in normal cells. In fact, β-catenin acts as an oncogene and modulates transcription of genes to drive cancer initiation, progression, survival, and relapse. All of the existing information regarding abnormal expression and function of β-catenin in cancer makes it a putative drug target since its targeting will negatively affect both tumor metastasis and stem cell maintenance. Transcriptional target genes of β-catenin involve several EMT-promoting genes, including Slug. Expression of Slug has been shown to be associated with breast tumor recurrence and metastasis[13–15]. Pro-migratory transcription factor Slug (EMT-TF), which can repress E-cadherin, triggers the steps of desmosomal disruption, cell spreading, and partial separation at cell-cell borders, which comprise the first and necessary phase of the EMT process.
Recently, the use of natural phytochemicals to impede tumor metastasis via multiple targets that regulate the migration potential of tumor cells has gained immense importance. In this regard, curcumin, a dietary polyphenol, has been studied extensively as a chemopreventive agent in a variety of cancers, including those of the breast, liver, prostate, hematological, gastrointestinal, and colorectal cancers, and as an inhibitor of metastasis. In a recent report, curcumin was shown to selectively inhibit the growth and self-renewal of breast CSCs (bCSCs). However, there are no reports regarding the contribution of curcumin in bCSC migration.
The present study describes (i) the mechanisms governing the augmented migration potential of bCSCs, which (ii) possibly associates with tumor aggressiveness and is largely attributable to the inherent downregulation of the anti-migratory tumor suppressor protein, E-cadherin, in bCSCs, and (iii) the role of curcumin in modulating the same. A search for the upstream mechanism revealed higher nuclear translocation and transcriptional activity of β-catenin resulting from disruption of E-cadherin/β-catenin complex formation in bCSCs in comparison with non-stem tumor cells. Upregulation of nuclear β-catenin resulted in the augmentation of Slug gene expression that, in turn, repressed E-cadherin expression. In contrast, exposure to curcumin inhibited the nuclear translocation of β-catenin, thereby hampering the activation of its EMT-promoting target genes, including Slug. Resultant upregulation of E-cadherin led to increase in E-cadherin/β-catenin complex formation, which further inhibited nuclear translocation of β-catenin. As a consequence, the E-cadherin/β-catenin negative feedback loop was amplified upon curcumin exposure, which reportedly inhibits EMT on one hand and promotes cell-cell adherens junction formation on the other. These results suggest that curcumin-mediated inhibition of bCSC migration may be a possible way for achieving CSC-targeted therapy to better fight invasive breast cancers.
Materials and methods
Primary tissue culture
Primary human breast cancer tissue samples used in this study were obtained with informed consent from all patients from Department of Surgery, Bankura Sammilani Medical College, Bankura, India, in accordance with the Institutional Human Ethics Committee (approval letter CNMC/ETHI/162/P/2010), and the associated research and analyses were done at Bose Institute, Kolkata, India, in compliance with the Bose Institute Human Ethics Committee (approval letter BIHEC/2010-11/11). These tumors were exclusively primary-site cancers that had not been treated with either chemotherapy or radiation. The selected cases consisted of three primary breast cancer patients of each group. The specimens were washed with phosphate-buffered saline (PBS), cut into small pieces (5 × 5 mm in size), and immersed in a mixture of colloagenase (10%; Calbiochem, now part of EMD Biosciences, Inc., San Diego, CA, USA) and hyaluronidase (0.5 mg/mL; Calbiochem) for 12 to 16 hours at 37°C on orbital shaker. The contents were centrifuged at 80 g for 30 seconds at room temperature. The supernatant, comprising mammary fibroblasts, was discarded, and to the pellet pre-warmed 0.125% trypsin-EDTA was added. The mixture was gently pipetted and kept for 30 minutes at 37°C. Finally, the pellet obtained was washed with cold Hanks’ buffer saline with 2% fetal bovine serum and centrifuged at 450 g for 5 minutes at room temperature. The single cells were seeded on poly-L lysine-coated dishes and cultured in medium containing growth factors, 0.1 ng/mL human recombinant epidermal growth factor, 5 μg/mL insulin, 0.5 μg/mL hydrocortisone, 50 μg/mL gentamycin, 50 ng/mL amphotericin-B, and 15 μg/mL bovine pituitary extract at 37°C. Medium was replaced every 4 days, and passages were done when the cells reached 80% confluence.
Cell culture and treatment
Human breast cancer cell lines MCF-7 and T47D were obtained from the National Centre for Cell Science (Pune, India). The cells were routinely maintained in complete Dulbecco’s modified Eagle’s medium (DMEM) supplemented with 10% heat-inactivated fetal bovine serum (FBS), penicillin (100 units/mL), and streptomycin (100 l g/mL) at 37°C in a humidified incubator containing 5% CO2. Cells were allowed to reach confluency before use. Cells were maintained in an exponential growth phase for all experiments. All cells were re-plated in fresh complete serum-free medium for 24 hours prior to the experiments. Viable cell numbers were determined by Trypan blue dye exclusion test. Cells were treated with different doses (5, 10, 15, and 20 μM) of curcumin (Sigma-Aldrich, St. Louis, MO, USA) for 24 hours to select the optimum non-apoptotic dose of curcumin (15 μm) which significantly abrogates migration potential of bCSCs. An equivalent amount of carrier (dimethyl sulfoxide) was added to untreated/control cells. To rule out cell proliferation, all migration assays were performed in the presence of 10 μg/mL mitomycin C.
For mammosphere culture, MCF-7/T47D cells were seeded at 2.5 × 104 cells per well in sixwell Ultralow Adherence plates (Corning Inc., Corning, NY, USA) in DMEM/F12 with 5 μg/mL bovine insulin (Sigma-Aldrich), 20 ng/mL recombinant epidermal growth factor, 20 ng/mL basic fibroblast growth factor, B27 supplement (BD Biosciences, San Jose, CA, USA), and 0.4% bovine serum albumin (BSA) as previously described. Primary/1° and secondary/2° mammosphere formation was achieved by using weekly trypsinization and dissociation followed by reseeding in mammosphere media at 2.5 × 104 cells per well into Ultralow Adherence sixwell plates.
Cell viability assay
Cell viability assay was performed by using Trypan blue dye exclusion assay. Mammospheres were treated with different doses of curcumin for 24 hours. Thereafter, the numbers of viable cells were counted by Trypan blue dye exclusion by using a hemocytometer. The results were expressed as percentage relative to the control cells.
Expression of human bCSC markers CD44 and CD24 were analyzed by flow cytometric study in different stages of breast cancer tissue as well as in MCF-7/T47D cells and primary and secondary mammospheres by using CD44-FITC and CD24-PE antibodies (BD Biosciences). bCSCs were flow-cytometrically sorted from primary breast tumors on the basis of the cell surface phenotype CD44+/CD24-/low. De-differentiation, drug resistance, and stemness phenomena were quantified flow-cytometrically by measuring mean fluorescence intensities of de-differentiation markers Oct-4-PerCP-Cy5.5, Nanog-PE, and Sox-2-Alexa Fluor-647; drug-resistance markers MRP1-FITC, ABCG2-PE, and ALDH1-FITC (BD Biosciences); and epithelial markers cytokeratin-18-PE and cytokeratin-19-PE (Santa Cruz Biotechnology, Inc., Santa Cruz, CA, USA). Expression levels of E-cadherin, β-catenin, and Slug (Santa Cruz Biotechnology, Inc.) were determined with respective primary antibodies conjugated with PE as previously described.
For immunofluorescence, cells were grown on sterile glass coverslips at 37°C for 24 hours. Cells after treatment were washed briefly with PBS and fixed with 4% formaldehyde for 20 minutes at 37°C and permeabilized with Triton X100 (for intracellular protein expression analysis). Thereafter, cells were blocked for 2 hours in a blocking buffer (10% BSA in PBS) and incubated for another hour in PBS with 1.5% BSA containing anti-CD44/CD24/E-cadherin/β-catenin/phospho-FAK antibody (Santa Cruz Biotechnology, Inc.). After washing in PBS, cells were incubated with FITC/PE-conjugated secondary antibodies in PBS with 1.5% BSA for 45 minutes at 37°C in the dark. 4′-6-diamidino-2-phenylindole (DAPI) was used for nuclear staining. Coverslips were washed with PBS and mounted on microscopy glass slides with 90% glycerol in PBS. Images were acquired by using a confocal microscope (Carl Zeiss, Jena, Germany).
To determine the expression of bCSC markers in the migrating versus non-migrating fraction of MCF-7 cells, bi-directional wound-healing assay was performed. Briefly, cells were grown to confluency on sterile glass coverslips, after which a sterile 10-μL tip was used to scratch the monolayer of cells to form a bi-directional wound. Cells were allowed to migrate for 24 hours and then the coverslips were used for immunofluorescence staining.
Transwell migration assay
Transwell migration assay was performed by using 8.0-μm cell culture inserts (BD Biosciences) to test the migratory ability of primary breast cancer cells, MCF-7/T47D cells, and mammosphere-forming cells. Cells were seeded at 2.5 × 105 cells per well in serum-free DMEM in the upper chamber of 12-well plates and allowed to migrate for 8 hours toward DMEM containing 10% FBS in the lower chamber. After 8 hours, the cells in the upper chamber were removed with a cotton swab and the migrated cells in the lower surface of the membrane were fixed and stained with giemsa or the migrated fraction of 2° mammospheres were collected from the under-surface of the membranes after 24-hour migration assay for flow cytometry. Images were acquired with a brightfield microscope (Leica, Wetzlar, Germany) at 20× magnification. To quantify migratory cells, three independent fields were analyzed by using ImageJ software (National Institutes of Health, Bethesda, MD, USA). Migration was expressed as percentage of cells migrated. For the same, the percentage of cells that migrated in the control set of each relevant experiment was taken as 100%.
Cell adhesion assay
For evaluating cell adhesion property, cells were trypsinized by using trypsin-EDTA and resuspended in DMEM at a density of 0.8 × 106 cells per milliliter. These cell suspensions were allowed to recover from the trypsinization for 1 hour at 37°C in a humidified incubator containing 5% CO2. They were mixed gently every 15 minutes during this hour of conditioning. After every 15 minutes of incubation, the dishes were removed from the incubator, and the medium containing unattached cells was removed. Images were acquired with an Olympus BX700 inverted microscope (Olympus, Tokyo, Japan) at 20× magnification. To quantify cell adhesion, the number of unattached cells at 1 hour was determined by counting three independent fields. Attachment (at 1 hour) was expressed as percentage of cells adhered, and the percentage of the control set of each relevant experiment was taken as 100%.
Cell spreading assay
Spreading of the attached cells was monitored. At various time intervals (for every 30 minutes up to 3 hours), cells were imaged by using an Olympus BX700 inverted microscope (Olympus). Images of multiple fields were captured from each experimental set at 40× magnification. From the phase-contrast images, individual cell boundaries were marked with the free-hand tool of ImageJ, and the area within the closed boundary of each cell was quantified by using the analysis tool of ImageJ. Cell spreading (at 3 hours) was expressed as mean circularity of the cells. As confirmation assay for cell adhesion and spreading, MCF-7 cells and 2° mammosphere cells were plated on fibronectin (50 μg/mL)-coated surface, and focal adhesions were stained and quantified by immunofluorescence staining for phospho-FAK. In fact, phospho-FAK-enriched clusters at lamellipodia were considered as focal adhesion complex. Focal adhesion segmentation and size measurement were done by using ImageJ software.
Three-dimensional invasion assay
Three-dimensional (3D) invasion assay of mammospheres was performed in 96-well plates. Each well was first coated with 80 μL matrigel (BD Biosciences) in 3:1 ratio with complete DMEM. Mammospheres with or without curcumin/small interfering RNA (siRNA)/short hairpin RNA (shRNA)/cDNA treatment were mixed with matrigel (6:1) and added to the previously coated wells. Thereafter, the mammospheres were allowed to invade for 48 hours. Images were photographed by using an Olympus BX700 inverted microscope (Olympus) at 20× magnification. Data were analyzed by using ImageJ software as area invaded and were expressed as percentage relative to the control set, the value of which was taken as 100%.
Western blotting and co-immunoprecipitation
To obtain whole cell lysates, cells were homogenized in buffer (20 mM Hepes, pH 7.5, 10 mM KCl, 1.5 mM MgCl2, 1 mM Na-EDTA, 1 mM Na-EGTA, and 1 mM DTT). All buffers were supplemented with protease and phosphatase inhibitor cocktail[24, 25]. Protein concentrations were estimated by using Lowry’s method. An equal amount of protein (50 μg) was loaded for Western blotting. For direct Western blot analysis, the cell lysates or the particular fractions were separated by SDS-PAGE, transferred to polyvinylidene difluoride membrane (Millipore, Darmstadt, Germany), and probed with specific antibodies like anti-E-cadherin, anti-β-catenin, anti-histone H1, anti-cyclin-D1, anti-c-myc, anti-slug, anti-vimentin, anti-MMP-2, anti-MMP-9, anti-twist, anti-Snail, and anti-α-Actin (Santa Cruz Biotechnology, Inc.). The protein of interest was visualized by chemiluminescence (GE Biosciences, Piscataway, NJ, USA). To study the interaction between E-cadherin and β-catenin, β-catenin immunocomplex from whole cell lysate was purified by using β-catenin antibody and protein A-Sepharose beads (Invitrogen, Frederick, MD, USA). The immunopurified protein was immunoblotted with E-cadherin antibody. The protein of interest was visualized by chemi-luminescence. Equivalent protein loading was verified by using anti-α-actin/Histone H1 antibody (Santa Cruz Biotechnology, Inc.).
Reverse transcription-polymerase chain reaction assay
Two micrograms of the total RNA, extracted from cells with TRIzol reagent (Invitrogen, Carlsbad, CA, USA), was reverse-transcribed and subjected to polymerase chain reaction (PCR) with enzymes and reagents of the RTplusPCR system (Eppendorf, Hamburg, Germany) by using GeneAmpPCR 2720 (Applied Biosystems, Foster City, CA, USA). The cDNAs were amplified with specific primers for E-cadherin (forward-CACCTGGAGAGAGGCCATGT, reverse-TGGGAAACAT-GAGCAGCTCT) and glyceraldehyde 3-phosphate dehydrogenase (GAPDH) (forward-CGT-ATTGGGCGCCTGGTCAC, reverse-ATGATGACCCTTT-TGGCTCC).
Plasmid and small interfering RNA/short hairpin RNA transfections
Cells were transfected separately with 300 pmol of E-cadherin shRNA (Addgene, Cambridge, MA, USA) or Slug siRNA (Santa Cruz Biotechnology, Inc.) by using Lipofectamine 2000 (Invitrogen). The levels of respective proteins were estimated by Western blotting. The Slug cDNA (Addgene) plasmid was used for overexpression studies. The Slug cDNA clone was introduced in cells by using Lipofectamine 2000. Stably expressing clones were isolated by limiting dilution and selection with G418 sulphate (Cellgro, a brand of Mediatech, Inc., Manassas, VA, USA) at a concentration of 400 μg/mL, and cells surviving this treatment were cloned and screened by Western blot analysis with specific antibodies.
Tissues were dissected out; fixed in Bouin’s fixative overnight; cryoprotected in 10% (2 hours), 20% (2 hours), and 30% (overnight) sucrose solution in PBS at 4°C; and frozen with expanding CO2, and serial sections were cut on a cryostat (CM1850; Leica) at 15-μm thickness. The tissue sections were washed in PBS (pH 7.45) for 15 minutes and treated with 1% BSA in PBS containing 0.1% Triton X-100. Sections were incubated overnight at 25°C in a humid atmosphere with primary antibodies against E-cadherin (1:100; Santa Cruz Biotechnology, Inc.) diluted in PBS containing and 1% BSA. Sections were rinsed in PBS for 10 minutes and incubated with biotinylated anti-mouse IgG (Sigma-Aldrich; 1:100) for 1 hour, followed by ExtrAvidin-peroxidase conjugate (Sigma-Aldrich; 1:100) for 40 minutes. 3-Amino-9-ethyl carbazole was used as chromogen (Sigma-Aldrich; 1:100) to visualize the reaction product. Thereafter, sections were counterstained with hematoxylin (1:1; Himedia, Mumbai, India). Finally, sections were washed in distilled water and mounted in glycerol gelatin. Images were acquired with a brightfield microscope (Leica) at 10× magnification.
Values are shown as standard error of mean unless otherwise indicated. Comparison of multiple experimental groups was performed by two-way analysis-of-variance test. Data were analyzed; when appropriate, significance of the differences between mean values was determined by a Student’s t test. Results were considered significant at a P value of not more than 0.05.
Breast cancer stem cells, being highly migratory, are linked with aggressiveness of the disease
At this stage, we considered the possibility that, since the mammosphere is a heterogeneous population of cells consisting of both CSCs and non-stem cancer cells, the migrated population of the mammosphere might be a heterogeneous one. It therefore becomes debatable whether the aggravated migration property of mammospheres is the contribution of bCSCs or of non-stem cancer cells. To get the answer, the migrated cells of the mammospheres were collected from the under-surface of the membranes, and flow cytometric analyses were performed to characterize the migrated cells. Results of Figure 3E demonstrated that the majority of the migrating cells of the mammospheres were bCSCs for both the cell lines, that is, 83.67% ± 2.90% bCSCs for mammospheres of MCF-7 (P <0.001) and 80.33% ± 3.48% (P <0.001) bCSCs for mammospheres of T47D. These results validate that bCSCs are endowed with aggravated migration potential as compared with the rest of the non-stem tumor population.
bCSCs exhibit enhanced migration potential through suppression of the EMT marker, E-cadherin
Suppression of E-cadherin expression in bCSCs is associated with greater nuclear translocation and transcriptional activity of β-catenin
Activation of β-catenin/Slug pathway hinders expression of E-cadherin in bCSCs
It is reported that both the EMT-promoting transcription factors, Slug and Snail, the transcriptional target genes of β-catenin, are potent transcriptional repressors of the E-cadherin gene. Our results above, showing significantly greater Slug gene expression in mammospheres than in MCF-7 cells with very low expression levels of Snail in both of the cell types, tempted us to evaluate whether the repression of E-cadherin in bCSCs was mediated through the β-catenin/Slug pathway. To that end, siRNA-mediated silencing of Slug in mammospheres resulted in restoration of E-cadherin expression at both protein and mRNA levels (Figure 5E). Under such conditions, the migration potential of the mammospheres was simultaneously retarded as was assessed by monitoring (i) adhesion, that is, 52.67% ± 5.61% cells adhered in Slug-silenced mammospheres as compared with the control set (100%, P <0.01) (Figure 5F); (ii) spreading, that is, 0.49 ± 0.03 and 0.7 ± 0.04 mean circularity in control and Slug-ablated mammospheres, respectively (P <0.05; Figure 5G, left panel); (iii) invasion, that is, 46.67% ± 4.05% invasion in Slug-siRNA-transfected mammospheres as compared with control, that is, (100%, P <0.001) (Figure 5G, middle panel); and (iv) transwell migration, that is, 37.33% ± 5.04% in Slug knocked-down mammospheres as compared with 100% migration of the control (P <0.001; Figure 5G, right panel) of MCF-7 cells. The effect of Slug silencing in migration potential was further validated in mammospheres of T47D cells (28% ± 5.69% migration as compared with control, P <0.001, Figure 5G, right panel). All of these results confirmed that E-cadherin repression in bCSCs results from the activation of the β-catenin/Slug pathway.
Curcumin abrogates bCSC migration in a dose-dependent manner by restoring EMT-suppressor, E-cadherin
Curcumin retards activation of β-catenin/Slug pathway in bCSCs thereby restoring E-cadherin
Our findings altogether establish a novel role of curcumin in abrogating bCSC migration by restoring the expression of the EMT suppressor E-cadherin, which is normally suppressed in these highly migratory cells, via amplification of E-cadherin/β-catenin negative feedback loop.
In the present study, we have disclosed the inhibiting effect of the phytochemical curcumin on migration property of bCSCs. Curcumin is reportedly a potent anti-cancer agent which exerts its anti-cancer effects in multiple ways, including negative regulation of cancer metastasis, angiogenesis, apoptosis, cell-cycle progression, inflammation, and multi-drug resistance[24, 25, 38, 39]. In addition, curcumin can target resistant CSCs by inducing apoptosis. In this study, we assessed the highly aggravated migration potential of bCSCs as compared with the non-stem tumor cells, which comprise the vast majority of the tumor. Aggressiveness of CSCs may justify the gradual increase in the CSC content of the primary tumor with increasing aggressiveness. Interestingly, curcumin retarded the migration potential of the bCSCs by restoring the expression of the inherently repressed EMT-suppressor, E-cadherin. An in-depth study revealed that the curcumin effect was materialized by the downregulation of nuclear β-catenin expression, which in turn negatively affected its pro-migratory transcriptional role, resulting in the diminished expression of its target gene Slug, a transcriptional repressor of E-cadherin. From another view point, curcumin treatment rendered greater E-cadherin/β-catenin complex formation which further perturbed the nuclear import of β-catenin. Thus, our work elucidates a thus-far-unknown novel role of curcumin in targeting the aggravated migration property of bCSCs by amplifying the E-cadherin/β-catenin negative feedback loop.
According to the recent studies, CSCs not only are tumor initiators but also are culprits of tumor metastasis. Importantly, these CSCs are largely evasive of the currently existing cancer treatment modalities. This major drawback of existing treatment strategies has led to the growth of considerable interest in alternative treatments using natural remedies since they are more tolerated and cause no significant toxicity as compared with the side effects of chemotherapeutic treatments. Curcumin, the Indian spice derived from the rhizomes of turmeric (Curcuma longa), has been intensively studied as a cancer chemopreventive agent in a wide range of cancer models[38, 39, 43]. A plethora of molecular targets and signaling pathways have been shown to be modulated by curcumin, resulting in inhibition of cancer cell proliferation, invasion, metastasis, angiogenesis, and induction of apoptosis[38, 39]. In recent years, curcumin has also been reported to exert its anti-cancer effects on CSCs. A very recent report demonstrated that curcumin targets breast cancer stem-like cells with micro-tentacles that persist in mammospheres and promote reattachment. However, there are no detail studies on the anti-migratory effects of curcumin on CSCs.
Metastasis is responsible for more than 90% of cancer-associated mortality, thereby justifying the clinical need to prevent or target metastasis[45, 46]. It is known that EMT is an essential developmental process that enables reprogramming of polarized epithelial cells toward a mesenchymal motile phenotype. In normal adult tissues, the typically dormant EMT program is reactivated during wound repair and tissue regeneration. In contrast, the non-metastatic cancer cells may undergo the EMT program to attain the migratory and invasive potential required for metastatic progression. Recently, gene expression patterns in human cancers have indicated that de-differentiated cancer cells combine EMT properties with a stem-cell like phenotype[11, 49]. A direct molecular link between EMT and stemness was demonstrated by the observations that EMT activators, such as transforming growth factor-beta 1 (TGFβ1), can co-induce EMT and stemness properties, thereby linking the EMT and CSC concept. Cancer cells that undergo EMT lose epithelial polarity and acquire invasive properties and stem cell-like features, which are believed to prelude metastasis. This correlation between EMT and CSCs suggests that the treatment strategies which target EMT regimen may virtually restrain both CSCs and metastatic potential of the tumor. In our present study, we report a novel function of curcumin in disrupting this complex ‘EMT-ambience’ of bCSCs which is also responsible for their aggravated migratory property. Therefore, our results are in keeping with a recent concept suggesting that CSCs have characteristics of post-EMT cancer cells and that these features further aid these CSCs for successful metastatic colonization. Targeting this transition (EMT) among CSCs by curcumin therefore opens a new arena for the treatment of highly malignant breast cancers.
Loss of E-cadherin-mediated cell adhesion is one of the key mechanisms involved in metastatic conversion of epithelial cells and EMT. Numerous studies have described a partial or complete loss of E-cadherin during cancer progression, which is often correlated with an unfavorable prognosis, confirming E-cadherin to be a caretaker of the epithelial state. One of the probable mechanisms involved in E-cadherin dysfunction, especially loss of its expression and consequent promotion of tumor progression, is through β-catenin signaling. As the main binding partner of β-catenin, E-cadherin plays a pivotal role in β-catenin stabilization and function. Their functional complex formation is necessary for adhesion and the maintenance of epithelial cell layers. The loss of E-cadherin results in nuclear localization of endogenous β-catenin. On the other hand, E-cadherin could potentially antagonize signaling activity of β-catenin by sequestering β-catenin at the membrane, thus keeping it away from the nucleus, as well as by competing with LEF-1 for the same binding sites on β-catenin. If E-cadherin fails to associate with β-catenin, E-cadherin is retained in the endoplasmic reticulum, where it is subsequently degraded. A functional cadherin-catenin complex is therefore important for maintaining cellular integrity. In fact, increased concentration of free β-catenin in the cytoplasm promotes its binding to the LEF/TCF family of DNA-binding proteins. As a result, β-catenin translocates to the nucleus, where it transcriptionally activates specific target genes. Accumulating evidence suggests that several transcription factors, including Slug and Snail, both of which are transcriptional targets of β-catenin, are implicated in E-cadherin repression and EMT. However, the expression of Snail is suppressed in estrogen receptor-positive (ER+) breast cancer cell lines like MCF-7 and T47D, whereas Slug has been proposed to be a likely in vivo repressor of E-cadherin as compared with Snail in breast carcinomas. A report from Hajra et al. further demonstrated that, in breast cancer cell lines, Slug expression correlates more strongly than snail expression with E-cadherin suppression. In keeping with these reports, our results also revealed low expression of Snail in the ER+ breast cancer cell line, MCF-7, while Slug played the key role in maintaining the aggravated migration potential of bCSCs.
In breast cancer, curcumin has also been shown to repress expression of Slug. More recently, a report on MCF-7 cells showed that the effect of curcumin on bCSCs is mediated through the inhibition of the self-renewal property of these cells by exerting potent inhibition on Wnt/β-catenin signaling. Here, we report the yet-unexplored anti-migratory effect of curcumin on bCSCs by restoration of E-cadherin expression, which is mediated through the negative regulation of the β-catenin/Slug pathway. In fact, curcumin restores the E-cadherin/β-catenin complex formation, which further impedes nuclear transport of β-catenin that in turn increases E-cadherin expression through inhibition of Slug, thereby accentuating the E-cadherin/β-catenin negative feedback loop. Cumulatively, curcumin targets bCSC migration by suppressing their EMT phenotype, which in general imparts higher migration potential to tumor cells.
We demonstrate for the first time, to the best of our knowledge, that the phytochemical curcumin inhibits the aggravated migration potential of bCSCs by perturbing commencement of EMT. This could be a very promising addition to traditional cancer treatments, including chemotherapy and radiotherapy, especially given the fact that most chemotherapeutic drugs and radiotherapy do not have the capability to eliminate CSCs. This combination strategy will open a new avenue for more effective therapies for highly invasive breast carcinomas.
aldehyde dehydrogenase isoform 1
breast cancer stem cell
bovine serum albumin
cancer stem cell
Dulbecco’s modified Eagle’s medium
focal adhesion kinase
fetal bovine serum
lymphoid enhancer factor
polymerase chain reaction
short hairpin RNA
small interfering RNA
This work was supported by research grants from the Council of Scientific and Industrial Research, the Department of Biotechnology (DBT), the Department of Science and Technology, and the DBT Post-doctoral Fellowship Program of the Government of India.
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