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Metastatic colorectal cancer remains a serious health concern with poor patient survival. Although 5-Fluorouracil (5-FU) or 5-FU plus oxaliplatin (FOLFOX) is the standard therapy for colorectal cancer, it has met with limited success. Recurrence of the tumor after chemotherapy could partly be explained by the enrichment of the chemo-resistant sub-population of cancer stem cells (CSCs) that possess the ability for self-renewal and differentiation into different lineages in the tumor. Therefore development of therapeutic strategies that target CSCs for successful treatment of this malignancy is warranted. The current investigation was undertaken to examine the effectiveness of the combination therapy of dasatinib (a Src inhibitor) and curcumin (a dietary agent with pleiotropic effect) in inhibiting the growth and other properties of carcinogenesis of chemo-resistant colon cancer cells that are enriched in CSCs sub-population. Remnants of spontaneous adenomas from APCMin +/- mice treated with dasatinib and/or curcumin were analyzed for several cancer stem cell markers (ALDH, CD44, CD133 and CD166). Human colon cancer cells HCT-116 (p53 wild type; K-ras mutant) and HT-29 (p53 mutant; K-ras wild type) were used to generate FOLFOX resistant (referred to as CR) cells. The effectiveness of the combination therapy in inhibiting growth, invasive potential and stemness was examined in colon cancer CR cells. The residual tumors from APCMin +/- mice treated with dasatinib and/or curcumin showed 80-90% decrease in the expression of the CSC markers ALDH, CD44, CD133, CD166. The colon cancer CR cells showed a higher expression of CSCs markers, cell invasion potential and ability to form colonospheres, compared to the corresponding parental cells. The combination therapy of dasatinib and curcumin demonstrated synergistic interactions in CR HCT-116 and CR HT-29 cells, as determined by Calcusyn analysis. The combinatorial therapy inhibited cellular growth, invasion and colonosphere formation and also reduced CSC population as evidenced by the decreased expression of CSC specific markers: CD133, CD44, CD166 and ALDH. Our data suggest that the combination therapy of dasatinib and curcumin may be a therapeutic strategy for re-emergence of chemo-resistant colon cancer by targeting CSC sub-population.
Colorectal cancer, the third most common cancer affecting men and women equally , remains a huge health concern. It is the second most common cause of cancer-related deaths in the United States and other developed countries. Although with early detection and surgical resection, the 5-year survival rate can reach 90%, nearly 50% of patients with colorectal carcinoma develop recurrent disease [2,3]. Most of the colon cancer deaths results from the metastatic spread of chemotherapy-resistant cells to the liver and other organs  and thus, metastasis remains a poor prognostic indicator .
Over the last decade, there has been a growing body of evidence that support the concept of cancer stem cell (CSC) model as an explanation for the initiation, progression and recurrence of cancer. Epithelial cancers including colorectal cancer are now believed to be diseases driven by a minor subpopulation of self renewing cancer stem cells (CSCs). CSCs also have the potential to invade and form distant metastasis [6-10]. Biologically distinct and relatively rare populations of tumor-initiating cells or CSCs have been detected by several methods and markers established in a variety of cancers, including the colon [11-13]. Furthermore, CSCs are known to show resistance to a number of conventional chemotherapies and thus play a significant role in recurrence of primary cancers. Most of the conventional treatment regimen target the non-CSCs population of the tumor and fail to eliminate the CSCs [8,14]. The remaining chemotherapy-resistant CSCs lead to chemotherapy-refractory tumor, and may explain the difficulty in complete eradication of cancer and/or recurrence. Therefore, development of therapeutic strategies that specifically target CSCs is warranted in reducing the risk of relapse and metastasis.
5-Fluorouracil (5-FU) or 5-FU plus oxaliplatin (FOLFOX) remains the mainstay of colorectal cancer chemotherapeutics. Although these chemotherapeutic regimens produce a response in majority of the cases, virtually all the responses are incomplete and emergence of resistance with recurrence of the cancer is universal. There is also a cost of additional toxicities, some of which are even fatal. Therefore, validation of a non-toxic agent that could improve upon the current chemotherapeutic regimen(s) would be highly desirable. In an attempt to develop an effective treatment strategy, a combination therapeutic regimen comprising of dasatinib and curcumin (diferuloylmethane), was therefore tested for its efficacy in inhibiting growth and eliminating the CSCs in chemo-resistant colon cancer cells.
Dasatinib is a highly potent inhibitor of Src kinases and Abl kinases [15,16] and is currently employed for imatinib resistant CML and (Ph+) ALL treatment [15,16]. In addition to hematological malignancies, dasatinib has been shown to be effective in solid tumors and demonstrate multiple effects like inhibition of cellular growth, migration and invasion [15-17]. Our recent studies demonstrate that dasatinib regulates growth of breast cancer cells by modulating EGFR signaling . Also, since multiple signaling pathways are deregulated in carcinogenesis, several therapeutic regimens that target multiple signaling are being investigated and developed. In this context, we have recently shown that dasatinib act synergistically with the pan-erbB inhibitor EBIP (ErbB inhibitory protein) as well as with curcumin in inhibiting several processes of carcinogenesis in breast and colon cancers [18,19]. The combination therapies were found to be highly effective in inhibiting cellular growth, colony formation, extracellular matrix invasion and attenuation of various signaling pathways [18,19].
Curcumin, the major active ingredient of turmeric, has been shown to inhibit chemically induced carcinogenesis in the skin, forestomach and colon when administered during initiation and/or post-initiation phases [20-23]. Development of azoxymethane-induced preneoplastic and neoplastic lesions of the colon is also inhibited in experimental animals fed a diet containing curcumin [24,25]. Curcumin has been shown to suppress various stages of colon carcinogenesis with no discernable toxicity [26,27] and prevent adenoma development in the intestinal tract of Min+/- mice, a model of human familial adenomatous polyposis . Furthermore, in a Phase I clinical trial, curcumin was shown to be effective in inhibiting tumor growth .
Herein, we demonstrate that curcumin synergizes with dasatinib to inhibit the growth of FOLFOX-resistant colon cancer cells that are highly enriched in CSCs. The combination therapy is also effective in inhibiting cell invasion and colonosphere formation, the latter of which is considered to be surrogate for tumor.
Remnants of spontaneous adenomas from APCMin +/- mice treated with dasatinib and/or curcumin were obtained from our previous study . In this study we have demonstrated the superior efficacy of the combination therapy in inhibiting the formation as well as inducing the regression of spontaneous adenomas in APCMin +/- mice than either agent alone. The tissues were processed for RNA isolation and analyzed for mRNA expression of various CSC markers.
Human colon cancer HCT-116 p53 wild type (p53 wild type; K-ras mutant), HT-29 (K-ras wild type; p53 mutant) and their FOLFOX resistant cell lines were used to investigate the efficacy of combined therapy of dasatinib and curcumin. HCT-116 and HT-29 cells were obtained from American Type Culture Collection (ATCC, Rockville, MD). The cells were maintained in tissue culture flasks in Dulbecco's modified Eagle medium (DMEM) in a humidified incubator at 37°C in an atmosphere of 95% air and 5% CO2. The cell culture medium was supplemented with 5% FBS and 1% antibiotic/antimycotic. FOLFOX resistant cell lines were generated in our laboratory (as reported previously) . Briefly, HCT-116 or HT-29 cells were incubated with a clinically relevant dose of FOLFOX (25 μM 5-FU and 0.625 μM oxaliplatin) for one week. The adherent cells, which survived the FOLFOX insult, were subjected to trypsin/EDTA treatment and allowed to grow in normal DMEM for 2 weeks. The surviving cells were then split and gradually exposed to increasing doses of FOLFOX to a maximal concentration of 250 μM 5-FU and 6.25 μM oxaliplatin for 2-3 weeks for each treatment period. Finally, the chemo-resistant cells were maintained in normal culture medium containing FOLFOX (50 μM 5-FU + 1.25 μM oxaliplatin). The medium was changed three times a week and the cells were passaged using trypsin/EDTA.
Inhibition of cell growth in response to dasatinib and or curcumin was examined by 3-(4,5-dimethyl-thiazol-2yl)-2,5-diphenyl-tetrazolium bromide (MTT) assay as described previously . Briefly, 5,000 cells/well were seeded into 96-well culture plates and treated with different doses of dasatinib and/or curcumin for 72 h. All CR cells were exposed to 50 μM 5-FU and 1.25 μM oxaliplatin with or without (control) dasatinib and/or curcumin. This treatment strategy was utilized in all subsequent experiments. The doses of dasatinib and curcumin for combination were chosen in fixed-ratio increments. The fraction of cells affected (Fa) by various treatments as determined by MTT assay, was utilized to generate dose response curves for dasatinib, curcumin and the combination therapy by employing Calcusyn software (Biosoft, Ferguson, MO). Further, Combination Indices (CI) were produced by Calcusyn software that utilizes the methodology applied by Chou and Talalay for formal synergy analyses . This method utilizes a multiple drug-effect equation derived from enzyme kinetics model in which the output is represented as combination indices (CI) and/or isobologram analysis. Calcusyn software defines synergy when CI value is < 1. Synergy was defined based on terminology of Chou . Based on CI values, the extent of synergism/antagonism may be determined. In brief, CI values between 0.9 and 0.85 would suggest a moderate synergy, whereas those in the range of 0.7 to 0.3 are indicative of clear synergistic interactions between the drugs. On the other hand, CI values in the range of 0.9 to 1.10 would suggest a near additive effect. All assays were performed in quadreplicates.
DRI is the measure of fold-decrease of individual agent when used in synergistic combination to achieve a given effect level compared with the doses of each drugs alone. The Calcusyn software was employed to calculate the DRI for dasatinib in CR cancer cell lines. The data generated from growth inhibition assays (Fa values for different combination doses) was utilized to determine DRIs.
Total RNA was extracted from parental and chemo-resistant HCT-116 cells using Trizol reagent according to the manufacturer's instructions. RNA concentration was measured spectrophotometrically at an optical density of 260 nm. Quantitative reverse transcription-polymerase chain reaction (RT-PCR) was performed using the GeneAmp RNA PCR Kit (Applied Biosystems, Foster City, CA). Briefly, 1 μg of purified RNA was reverse-transcribed and the transcribed RNA was diluted five times for quantitative PCR amplification of various cancer stem cell markers. Five microliters of complementary DNA products was amplified with SYBR Green Quantitative PCR Master Mix (Applied Biosystems). Table Table11 provides the list and sequences of the mouse and human specific primers used in the study. Reactions were carried out in Applied Biosystems 7500 Real-Time PCR System as described previously by Yu et al. . The quantitation of the marker gene was normalized to amplification of β-actin and subsequently expressed as relative to untreated control.
Parental (control) and chemo-resistant colon cancer cells were subjected to direct immunofluorescence staining followed by flow cytometric analyses. Briefly, the cells were harvested and washed with PBS. Two million cells were suspended in 90 μl of PBS containing 0.5% BSA for 10 minutes at room temperature followed by the addition of 10 μl of PerCP cy5.5 fluorescent dye conjugated to CD44 and/or phyco-erythrin conjugated CD-166 monoclonal antibody (Santa Cruz Biotechnology, Santa Cruz, CA) and incubated for 30 minutes in the dark, at room temperature. The samples were then washed and analyzed using a FACS DiVa (BD, San Jose, CA).
To examine the effects of combination therapy on the formation of colonospheres by chemo-resistant cells, the ability of cell lines to form spheres in suspension was evaluated as described by Liu et al , with minor optimizations. Briefly, colonospheres were generated by incubating CR HCT-116 cells at a concentration of 250 cells per 100 μL in serum-free stem cell medium (SCM) containing DMEM/F12 (1:1) in 96-well ultra low-attachment plates (Corning Inc, Lowell, MA). The stem cell medium was supplemented with B27 (Life Technologies, Gaithersburg, MD), 20 ng/ml EGF (Sigma, St Louis, MO), 10 ng/ml fibroblast growth factor (Sigma), and antibiotic/antimycotic. After 24 h of cell seeding, dasatinib(1 μM) and curcumin(10 μM) were added to each well. The colonospheres formed in 10 days were photographed for five to six microscopic fields under a 10× objective. The colonospheres were further evaluated for their size by measuring the widest area of the sphere.
Invasion assay was performed as described by Nautiyal et al  using a colorimetric assay from the Chemicon International Inc. (Temecula, CA, USA). The kit utilizes ECMatrix™, a reconstituted basement membrane matrix of proteins. In brief, 5,000 CR HCT-116 cells were seeded in the insert with or without dasatinib (1 μM) and curcumin (10 μM), subsequently incubated at 37°C for 72 h. The inserts contained an 8 μm pore size polycarbonate membrane covered with a thin layer of EMatrix™. The ECM layer occluded the membrane pores, blocking the non-invasive cells from migrating through. However, invading cells migrated through the ECM layer and could be found attached to the bottom of polycarbonate layer. At the end of the incubation, non-invading cells were gently removed using a cotton-tipped swab from interior of the inserts. The invasive cells on the lower surface of inserts were stained with 500 μl of stain. For quantitation of invasive potential, the stained cells were solubilized with 200 μl of 10% acetic acid and a consistent volume of dye/solute mixture was read at 570 nm.
Unless otherwise stated, data were expressed as mean ± SD. Where applicable, the results were compared by using the unpaired, two-tailed Student t-test, as implemented by Excel 2007 (Microsoft Corp., Redmond, WA). p-value smaller than 0.05 was considered statistically significant.
Currently, CSCs are identified by specific surface epitopes. Colorectal CSCs cells were initially characterized by those expressing CD133 and subsequently by the expression of other surface markers such as CD44, CD166 and EpCAM/ESA (epithelial cell adhesion molecule/epithelial-specific antigen) . More recently, aldehyde dehydrogenase 1 (ALDH1) which is a detoxifying enzyme  has been identified as a specific marker for normal and malignant human colonic stem cells . ALDH1-positive cells, which are sparse and limited to the crypt bottom where stem cells reside, increase with progression of normal epithelium to adenoma to carcinoma . We have recently reported that dasatinib in combination with curcumin is highly effective in inhibiting cellular growth and transformation properties in vitro and induces regression of over 90% of the spontaneous intestinal adenomas in APCMin+/- mice . This led to our interest in investigating the efficacy of the combined therapy in targeting CSCs that are implicated in the processes of chemo-resistance and recurrence of cancer. The initial experiment was carried out to evaluate the effectiveness of the combination therapy in inhibiting the growth of intestinal CSCs. For this, we utilized adenoma remnants derived from our previous study and examined the relative expression of various CSC specific markers. Figure Figure11 shows a marked 80-90% reduction in the expression of the CSC markers in response to the combination therapy, suggesting that the combination of dasatinib and curcumin is highly effective in reducing the cancer stem cell population in adenomas, the precursor for adenocarcinoma. Although dasatinib has met with limited success in solid tumors, our observation that the expression of CSC markers was greatly inhibited by dasatinib alone (Figure (Figure1)1) provides a rationale for utilizing this drug in combination with more potent growth inhibitory agents like curcumin to achieve a superior anti-tumor response.
In an attempt to characterize the chemo-resistant (CR) cells, the expression of CD133, CD44, CD166 and ALDH1 was quantitated relative to the parent cell line (Figure (Figure2A).2A). CR HCT-116 cells show higher expression of each of these cancer stem cell markers than the parental HCT-116 cells. CR colon cancer cells were also investigated for dual staining for surface markers that play significant role in adhesion, namely CD44 and CD166. Both CR HCT-116 and CR HT-29 cells show higher proportion of cells expressing the two CSC markers concurrently (Figure (Figure2B).2B). Although the population of dual staining cells was higher for HCT-116 cells, the relative increase was much higher in CR HT-29 cells (~6 time the parent cells) (Figure (Figure2B).2B). This suggests a higher population of CSCs in chemo-resistant cells. Therefore, we chose these cell lines as a model for testing our hypothesis.
We have postulated that the combination therapy of curcumin and dasatinib would be a superior therapeutic strategy for chemo-resistant colorectal cancer. In order to test our hypothesis we first evaluated the interactions between dasatinib and curcumin in chemo-resistant (CR) colon cancer cells. We performed synergy analysis in CR HCT-116 and CR HT-29 cells, as described previously . Dose response curves were generated for both agents in CR colon cancer cells using Calcusyn software (Biosoft, Ferguson, MO) (Figures (Figures3A3A and and3B).3B). In each CR cell line the combination therapy caused a greater growth inhibition than that achieved in response to a single agent (Figures (Figures3A3A and and3B).3B). As observed previously , the combination therapy was found to be more effective in HT-29 (p53 mutant) cells than HCT-116 cells.
The fraction of cells affected in response to each treatment was thus utilized to perform synergy analysis with Calcusyn software. The Combination Index (CI) as formulated by the software, revealed values of less than 1.0 indicating a synergistic interaction between the two agents at most of the dose combinations tested (Table (Table2).2). The results suggest that dasatinib and curcumin act synergistically to inhibit the growth of CR colon cancer cells. Since dasatinib and curcumin revealed synergistic interactions, the subsequent studies were performed with the combination of 1 μM dasatinib and 10 μM curcumin. Similar to our recent findings in parent cell lines , a higher synergy (lower CI value) was observed for lower dose combinations. Such synergistic interactions between various drugs provides an opportunity to reduce the concentrations of the individual drug(s) and thereby, reducing their associated toxicities.
Once the interaction between the two agents was found to be synergistic, we next sought to determine the DRI for dasatinib in CR colon cancer cells. Since combination index (CI) for both cell lines show strong synergy between dasatinib and curcumin, we performed DRI analysis for CR HCT-116 cells (Table (Table3).3). Our data show DRI values for dasatinib in the range from 13 to 25 for CR HCT-116 cells. The DRI data further demonstrated that when used in combination with dietary agent curcumin, dasatinib concentrations could be reduced significantly.
We next investigated whether the combination therapy would be effective in inhibiting the formation of colonosphere, a salient feature of cancer stem cells. The combination therapy was found to be highly effective in inhibiting the sphere forming potential of both CR HCT-116 and CR HT-29 cells (Figures (Figures4A4A and and4B).4B). At the end of 10-day experimental period we observed that while the control cells formed well-defined spheroids, the CR cells treated with the combination therapy showed significantly smaller spheres/spheroids (Figure (Figure4C).4C). The average sizes of colonospheres formed by the untreated CR HCT-116 and CR HT-29 cells were ~111 and 177 μm respectively (Figure (Figure4C).4C). In contrast, the average size of colonospheres formed in response to the combination therapy was 40 and 38 μm, respectively (Figure (Figure4C).4C). This suggests the current targeted therapy is highly effective in inhibiting the stemness properties of chemo-resistant colon cancer cells.
Chemo-resistant cells are thought to be more aggressive and have higher potential to invade through extracellular matrix leading to metastasis and spread of the primary malignancy than the parental cells. In view of this, we investigated the effectiveness of the current combination therapy in inhibiting the invasion potential of CR HCT-116 cells. Our results show that the chemo-resistant HCT-116 cells have higher potential to invade as compared to the corresponding parental cells and that they are highly susceptible to the combination therapy (Figure (Figure5).5). This suggests that the combination therapy of the two targeted agents may be effective in targeting the chemo-resistant colon cancer.
Since the combination therapy is effective in inducing inhibition of growth, colonosphere formation and extracellular invasion, we next sought to test if this regimen would be effective in reducing the cancer stem cell population. The expression of CSC markers CD133, CD44, CD166 and ALDH1 was determined in the CR HCT-116 cells treated with the combination therapy. There was a 25-30% decrease in the expression of each of the CSC marker (Figures (Figures2A2A and and2B).2B). Although the CR cells displayed a higher expression of CSC markers and a higher proportion of cells showed co-expression of CD44 and CD166 (Figures (Figures2A2A &2B), the combination therapy greatly decreased the expression of these proteins (Figure (Figure6).6). These findings suggest that the combination therapy is highly effective in reducing the CSC sub-population in the chemo-resistant colon cancer and may be utilized as a CSC targeted therapy for elimination of recurrence of colon cancer.
Metastatic colorectal cancer remains incurable, indicating a poor prognosis and overall survival of about 2 years in surgically unresectable disease. FOLFOX is the standard therapy for colorectal cancer with limited success. Oxaliplatin, a platinum based chemotherapeutic agent form platinum-DNA adducts and interferes with DNA replication leading to cell death . Development of resistance to FOLFOX is a common phenomenon leading to recurrence of the tumor. Src, a tyrosine kinase, that regulates diverse cellular processes, has been associated with various stages of cancer progression with an inverse co-relation with patient survival . Enhanced Src activity has been reported in > 70% colon cancer, though the highest activity is demonstrated in metastasis [40,41]. More recently, Src kinase has been implicated in drug resistance  and is shown to be a modulator of sensitivity to oxaliplatin . Pre-clinical evidence indicates that inhibition of Src renders the cancer cells susceptible to chemotherapies [44-46]. In light of these findings, investigations are being carried out to develop dasatinib, a highly potent Src inhibitor, as an adjuvant therapy for treatment of cancer along with inhibition of recurrence. However, administration of multiple therapeutic agents is often associated with additional toxicities which at times may be life threatening. Therefore, a combination with non-toxic dietary agent like curcumin is expected to provide a superior benefit. Curcumin, a phytochemical has been reported to have anti-tumor effects in various solid tumors . Curcumin has been shown to augment the effect of a number of chemotherapeutic agents, including doxorubicin and vincristine and has been shown to enhance the cellular accumulation of these drugs leading to increased sensitivity of the drug-resistant cancer cells [47,48]. We have demonstrated that the combination of curcumin and FOLFOX causes a marked inhibition of growth of colon cancer cells . More recently, we reported that curcumin is highly effective in sensitizing the FOLFOX surviving colon cancer cells . The chemo-resistant HCT-116 cells show increased expression of several biomarkers of CSCs, a greater ability to form colonies and colonospheres, indicating an increase in the CSCs population . We demonstrated that curcumin alone or in combination with FOLFOX markedly decreases CSCs, as determined by decreased expression of CSCs markers and colony as well as colonosphere formation .
In the current investigation, we utilized FOLFOX resistant cells derived from two colon cancer cell lines with different mutational status; HCT-116 p53 wild type (p53 wild type; K-ras mutant), HT-29 (K-ras wild type; p53 mutant). We have recently reported synergistic interaction between dasatinib and curcumin in parental HCT-116 and HT-29 cells . Herein, we report similar synergistic effects on the chemo-resistant derivatives of these cells. Interestingly, as revealed by the combination indices, like the parent cells, CR HT-29 cells also show a higher susceptibility to the combination therapy than CR HCT-116 cells. This can be explained on the basis of recent findings of Kopetz et al. . They demonstrated that in HT-29 cells, the expression of Src is greatly augmented in response to oxaliplatin, and thus the inhibition of Src by dasatinib imparts greater sensitivity to oxaliplatin. On the other hand, HCT-116 cells that did not demonstrate an increase in Src expression failed to show such synergy between the two agents. Our current finding supports the contention that cancer cells that are highly dependent on Src signaling will be more susceptible to Src-targeted combination therapy.
Development of dasatinib as a therapeutic agent has been hindered by the toxicities and associated adverse effects. Our data, for the first time, demonstrate that by using curcumin, dasatinib dose could be markedly reduced as evidenced by the DRI calculations. This is particularly significant in clinical situations where reduced toxicity towards the host is much sought after. These observations suggest that combining dietary agents to conventional chemotherapeutics is greatly beneficial in achieving better therapeutic effects.
Failure of current chemotherapies to eliminate CSCs is thought to be a major hurdle in treating colon cancer. CSCs possess the potential to self-renew as well as to differentiate into heterogenous population of cells within the tumor. They are currently identified by the expression of specific surface and cytoplasmic markers. Potential markers for colon CSCs include CD133, CD44, CD166 and ALDH1 . Although the functional importance of CD133 remains to be resolved , CD44 is a transmembrane glycoprotein that has a unique cell adhesion function. CD44 plays a role in cancer cell migration as well as matrix adhesion and is involved in increased tumor growth [50,51]. CD166 is another adhesion molecule whose functional role is unclear. However, the expression of CD166 is found to be increased in primary adenocarcinomas and is associated with shorter patient survival . Another marker with functional significance is aldehyde dehydrogenase 1 (ALDH1), which is a detoxifying metabolic enzyme, found to be associated with stem cell population . In addition to being a potential cancer stem cell marker , ALDH1 is proposed to be associated with chemo-resistance of the subset of cells that show CD44 and CD166 dual positivity . We have observed that the colon cancer cells that are continually exposed to FOLFOX lead to increased expression of CSC markers. Our current data demonstrate increased expression of CD133, CD44, CD166 and ALDH1 in chemo-resistant colon cancer cells. Dalerba et al. have reported that tumorigenicity is more specific and restricted to CSCs that express both CD44 and CD166 . Interestingly, we have observed that CR HCT-116 as well as CR HT-29 cells contain a higher proportion of cells that express both CD44 and CD166 than the corresponding parental cell lines. Taken together the results show that, the chemo-resistant colon cancer cells are enriched in CSCs. We also report that the remnants of spontaneous adenomas from mice treated with dasatinib and/or curcumin showed 80-90% decrease in the expression of the CSC markers ALDH1, CD44, CD133, CD166.
Our current data demonstrate that the combination therapy is highly effective in inhibiting the processes of carcinogenesis as evidenced by decreased colonosphere formation by the chemo-resistant cells that are highly enriched in CSCs. CR HCT-116 cells also show a higher invasive potential and greater susceptibility to the combination therapy, suggesting that this treatment could be an effective therapeutic strategy for targeting chemo-resistant cancer cells. Furthermore, the combination treatment is highly effective in eliminating the CSCs population in the CR HCT-116 colon cancer cells. The expression of CSC markers is significantly reduced in response to the combination therapy. Considering the fact that the combination therapy is highly effective in inhibiting stem cell population in primary tumors as well as chemo-resistant colon cancer cells, our current observation suggests that the targeted combination regimen could be a superior strategy in eliminating CSCs and may inhibit the re-emergence of colon cancer. Additionally, incorporation of curcumin, a phytochemical will enable us to achieve greater benefit with reduced drug toxicities. This dietary agent which is well tolerated, could be added to food and taken on a long-term basis to either prevent primary tumor formation or tumor recurrence .
5-FU: 5-Fluorouracil; ALDH1: aldehyde dehydrogenase 1; ATCC: American type culture collection; CI: combination indices; CML: chronic myelogenous leukemia; CSCs: cancer stem cells; CR: chemo-resistant; DMEM: Dulbecco's modified Eagle medium; EpCAM/ESA: epithelial cell adhesion/epithelial specific antigen; Fa: fraction of cells affected; FOLFOX: 5-FU plus oxaliplatin; MTT: 3-(4,5-dimethyl-thiazol-2yl)-2,5-diphenyl-tetrazolium bromide; PCR: Polymerase Chain Reaction; (Ph+) ALL: Philadelphia chromosome-positive acute lymphoblastic leukemia; RNA: ribo-nucleic acid; RT-PCR: Reverse transcription- polymerase chain reaction; SCM: stem cell media; SD: standard deviation.
None of the following authors have any conflict of interest: JN, SSK, YY, APNM.
JN carried out the experiments and wrote the manuscript. SSK helped in discussion and interpretation of the data. YY designed all the primers utilized in this manuscript. APNM, the principal investigator, was responsible for planning, designing, analysis of the data and overall supervision of the work and final preparation of the manuscript. All authors read and approved the final manuscript.
Jyoti Nautiyal, PhD; Postdoctoral Research Fellow, Department of Internal Medicine and Veterans Affairs Medical Center, Wayne State University, Detroit, MI 48201, USA. E-mail: moc.liamg@layituanitoyj.
Shailender S. Kanwar, Ph.D.: Postdoctoral Research Fellow, Department of Internal Medicine and Veterans Affairs Medical Center, Wayne State University, Detroit, MI 48201, USA. E-mail: moc.liamg@rawnakss
Yingjie Yu, M.D., Research Assistant Professor, Department of Internal Medicine and Veterans Affairs Medical Center, Wayne State University, Detroit, MI 48201, USA. E-mail: ude.enyaw@2415aa
Adhip P.N. Majumdar, Ph.D., D.Sc.: Professor and Senior Research Career Scientist, Department of Internal Medicine, Veterans Affairs Medical Center. E-mail: firstname.lastname@example.org
The work presented in this communication has been supported by grants to Dr Majumdar by the Department of Veterans Affairs (VA Merit Review) and NIH/NIA (AG014343).