Gemcitabine: An Alternative Treatment for Oxaliplatin-Resistant Colorectal Cancer

Simple Summary Colorectal cancer is the third most common cancer worldwide. The treatment of the advanced stages is based on poly-chemotherapies, including oxaliplatin. However, the development of resistance to chemotherapy is observed in 50% of cases, leading to treatment failures. A better understanding of the resistance mechanisms is therefore crucial to improve treatment efficiency and patient survival. In our previous work, showed that ROS production and the p38 MAPK pathway were strongly involved in resistance to oxaliplatin. In this study, we tested several chemotherapies and observed that only gemcitabine efficiently treated oxaliplatin-resistant cancer cells. Indeed, gemcitabine was able to induce apoptosis by inhibiting both the Akt and p38 MAPK pathways. Taken together, our results show that gemcitabine could be an interesting therapeutic option for patients with oxaliplatin-resistant tumors. Abstract Resistance to treatments is one of the leading causes of cancer therapy failure. Oxaliplatin is a standard chemotherapy used to treat metastatic colorectal cancer. However, its efficacy is greatly reduced by the development of resistances. In a previous study, we deciphered the mechanisms leading to oxaliplatin resistance and highlighted the roles played by ROS production and the p38 MAPK pathway in this phenomenon. In this report, we studied the effects of different chemotherapy molecules on our oxaliplatin-resistant cells to identify alternative treatments. Among all the studied molecules, gemcitabine was the only one to present a major cytotoxic effect on oxaliplatin-resistant cancer cells both in vivo and in vitro. However, the combination of oxaliplatin and gemcitabine did not present any major interest. Indeed, the study of combination efficiency using Chou and Talalay’s method showed no synergy between oxaliplatin and gemcitabine. Using PamGene technology to decipher gemcitabine’s effects on oxaliplatin-resistant cells, we were able to show that gemcitabine counteracts chemoresistance by strongly inhibiting the Akt and src/p38 MAPK pathways, leading to apoptosis induction and cell death. In view of these results, gemcitabine could be an interesting alternative therapy for patients with colorectal cancer not responding to oxaliplatin-based protocols such as FOLFOX.

[1]  M. Hattori,et al.  Colossolactone-G synergizes the anticancer properties of 5-fluorouracil and gemcitabine against colorectal cancer cells. , 2021, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

[2]  Xinghuan Wang,et al.  KNSTRN promotes tumorigenesis and gemcitabine resistance by activating AKT in bladder cancer , 2021, Oncogene.

[3]  G. Bossi,et al.  The p38 MAPK Signaling Activation in Colorectal Cancer upon Therapeutic Treatments , 2020, International journal of molecular sciences.

[4]  M. McKeage,et al.  Transport-Mediated Oxaliplatin Resistance Associated with Endogenous Overexpression of MRP2 in Caco-2 and PANC-1 Cells , 2019, Cancers.

[5]  H. Kovacic,et al.  Reversion of resistance to oxaliplatin by inhibition of p38 MAPK in colorectal cancer cell lines: involvement of the calpain / Nox1 pathway , 2017, Oncotarget.

[6]  Hua Chen,et al.  Targeted inhibition of the phosphoinositide 3-kinase impairs cell proliferation, survival, and invasion in colon cancer , 2017, OncoTargets and therapy.

[7]  A. Paci,et al.  Safety, tolerability and antitumour activity of LY2780301 (p70S6K/AKT inhibitor) in combination with gemcitabine in molecularly selected patients with advanced or metastatic cancer: a phase IB dose escalation study. , 2017, European journal of cancer.

[8]  M. Hjermstad,et al.  Health-related quality of life in patients with metastatic colorectal cancer, association with systemic inflammatory response and RAS and BRAF mutation status. , 2017, European journal of cancer.

[9]  M. Marangolo,et al.  Prolonged Pemetrexed Infusion Plus Gemcitabine in Refractory Metastatic Colorectal Cancer: Preclinical Rationale and Phase II Study Results , 2017, The oncologist.

[10]  E. Giovannetti,et al.  Phospho-Akt overexpression is prognostic and can be used to tailor the synergistic interaction of Akt inhibitors with gemcitabine in pancreatic cancer , 2017, Journal of Hematology & Oncology.

[11]  L. Leong,et al.  Phase I/II Trial of Anticarcinoembryonic Antigen Radioimmunotherapy, Gemcitabine, and Hepatic Arterial Infusion of Fluorodeoxyuridine Postresection of Liver Metastasis for Colorectal Carcinoma. , 2017, Cancer biotherapy & radiopharmaceuticals.

[12]  H. Shiraha,et al.  Loss of Runt-related transcription factor 3 induces resistance to 5-fluorouracil and cisplatin in hepatocellular carcinoma , 2016, Oncology reports.

[13]  Ho-Yyoung Lee,et al.  p38 MAPK-induced MDM2 degradation confers paclitaxel resistance through p53-mediated regulation of EGFR in human lung cancer cells , 2016, Oncotarget.

[14]  Ying Cheng,et al.  Detection of K-ras Mutations in Predicting Efficacy of Epidermal Growth Factor Receptor Tyrosine Kinase (EGFR-TK) Inhibitor in Patients with Metastatic Colorectal Cancer , 2015, PloS one.

[15]  S. Kim,et al.  Ratio of phosphorylated HSP27 to nonphosphorylated HSP27 biphasically acts as a determinant of cellular fate in gemcitabine-resistant pancreatic cancer cells. , 2015, Cellular signalling.

[16]  A. Jemal,et al.  Global cancer statistics, 2012 , 2015, CA: a cancer journal for clinicians.

[17]  Yang Ruan,et al.  SIRT1 Suppresses Doxorubicin-Induced Cardiotoxicity by Regulating the Oxidative Stress and p38MAPK Pathways , 2015, Cellular Physiology and Biochemistry.

[18]  G. Peters,et al.  A novel cytidine analog, RX-3117, shows potent efficacy in xenograft models, even in tumors that are resistant to gemcitabine. , 2014, Anticancer research.

[19]  C. Simone,et al.  p38α MAPK pathway: a key factor in colorectal cancer therapy and chemoresistance. , 2014, World journal of gastroenterology.

[20]  A. Elfiky,et al.  The role of Src in colon cancer and its therapeutic implications. , 2014, Clinical colorectal cancer.

[21]  M. Korc,et al.  DUSP1 Is a Novel Target for Enhancing Pancreatic Cancer Cell Sensitivity to Gemcitabine , 2014, PloS one.

[22]  Y. Yen,et al.  Dovitinib synergizes with oxaliplatin in suppressing cell proliferation and inducing apoptosis in colorectal cancer cells regardless of RAS-RAF mutation status , 2014, Molecular Cancer.

[23]  Xing-ye Wu,et al.  Oct-4 is required for an antiapoptotic behavior of chemoresistant colorectal cancer cells enriched for cancer stem cells: effects associated with STAT3/Survivin. , 2013, Cancer letters.

[24]  N. Traverso,et al.  p38MAPK inhibition: a new combined approach to reduce neuroblastoma resistance under etoposide treatment , 2013, Cell Death and Disease.

[25]  N. Zaffaroni,et al.  Modulation of sensitivity to antitumor agents by targeting the MAPK survival pathway. , 2012, Current pharmaceutical design.

[26]  R. Sánchez-Prieto,et al.  P38MAPK is a major determinant of the balance between apoptosis and autophagy triggered by 5-fluorouracil: implication in resistance , 2012, Oncogene.

[27]  H. Clevers,et al.  Comparative Proteomics of Colon Cancer Stem Cells and Differentiated Tumor Cells Identifies BIRC6 as a Potential Therapeutic Target* , 2011, Molecular & Cellular Proteomics.

[28]  A. Seifalian,et al.  Inhibition of the p38 MAPK pathway sensitises human colon cancer cells to 5-fluorouracil treatment. , 2011, International journal of oncology.

[29]  Y. Assaraf,et al.  Increased levels and defective glycosylation of MRPs in ovarian carcinoma cells resistant to oxaliplatin. , 2010, Biochemical pharmacology.

[30]  Sabine Tejpar,et al.  Prognostic role of KRAS and BRAF in stage II and III resected colon cancer: results of the translational study on the PETACC-3, EORTC 40993, SAKK 60-00 trial. , 2010, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[31]  T. Chou Drug combination studies and their synergy quantification using the Chou-Talalay method. , 2010, Cancer research.

[32]  F. Esposito,et al.  TRAP1, a novel mitochondrial chaperone responsible for multi-drug resistance and protection from apoptotis in human colorectal carcinoma cells. , 2009, Cancer letters.

[33]  D. Heimbrook,et al.  In vivo activity of novel capecitabine regimens alone and with bevacizumab and oxaliplatin in colorectal cancer xenograft models , 2009, Molecular Cancer Therapeutics.

[34]  L. Kèlland,et al.  The resurgence of platinum-based cancer chemotherapy , 2007, Nature Reviews Cancer.

[35]  Zhimin Tao,et al.  Caspase activation by anticancer drugs: the caspase storm. , 2007, Molecular pharmaceutics.

[36]  Ting-Chao Chou,et al.  Theoretical Basis, Experimental Design, and Computerized Simulation of Synergism and Antagonism in Drug Combination Studies , 2006, Pharmacological Reviews.

[37]  K. Syrigos,et al.  Multicenter Phase II Study of Gemcitabine and Oxaliplatin (GEMOX) as Second-Line Chemotherapy in Colorectal Cancer Patients Pretreated with 5-Fluorouracil plus Irinotecan , 2006, Oncology.

[38]  M. Benito,et al.  P38 alpha mitogen-activated protein kinase sensitizes cells to apoptosis induced by different stimuli. , 2003, Molecular biology of the cell.

[39]  T. Yamasaki,et al.  Synergistic augmentation of antimicrotubule agent-induced cytotoxicity by a phosphoinositide 3-kinase inhibitor in human malignant glioma cells. , 2003, Cancer research.

[40]  M. Barančík,et al.  SB203580, a specific inhibitor of p38-MAPK pathway, is a new reversal agent of P-glycoprotein-mediated multidrug resistance. , 2001, European Journal of Pharmaceutical Sciences.

[41]  M. Wolfson,et al.  The role of ERK 1/2 and p38 MAP-kinase pathways in taxol-induced apoptosis in human ovarian carcinoma cells. , 2001, Experimental cell research.

[42]  J. Tonkinson,et al.  Cell cycle modulation by a multitargeted antifolate, LY231514, increases the cytotoxicity and antitumor activity of gemcitabine in HT29 colon carcinoma. , 1999, Cancer research.

[43]  A. Jemal,et al.  Global cancer statistics , 2011, CA: a cancer journal for clinicians.

[44]  M. Ychou,et al.  Phase II trial of oxaliplatin as first-line chemotherapy in metastatic colorectal cancer patients. Digestive Group of French Federation of Cancer Centers. , 1998, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[45]  S. Allerheiligen,et al.  Preclinical, pharmacologic, and phase I studies of gemcitabine. , 1997, Seminars in oncology.

[46]  V. Heinemann,et al.  Gemcitabine: metabolism, mechanisms of action, and self-potentiation. , 1995, Seminars in oncology.

[47]  J. Fantini,et al.  Spontaneous and induced dome formation by two clonal cell populations derived from a human adenocarcinoma cell line, HT29. , 1986, Journal of cell science.

[48]  T. Chou,et al.  Quantitative analysis of dose-effect relationships: the combined effects of multiple drugs or enzyme inhibitors. , 1984, Advances in enzyme regulation.