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The effect of methylseleninic acid on paclitaxel efficacy in A2780 ovarian cancer cells

The effect of methylseleninic acid on paclitaxel efficacy in A2780 ovarian cancer cells
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摘要 Objective:The role of methylseleninic acid (MSeA), a selenium compound, has been documented in cancer chemoprevention. However, the therapeutic effect of MSeA in combination with paclitaxel, a chemotherapeutic agent used to treat ovarian cancer, is unknown. In this study, we investigated the effect of combination treatment of MSeA and paclitaxel against ovarian cancer cells. Methods:Ovarian cancer cells(A2780) were treated with different concentrations of MSeA, paclitaxel alone or in combination. The individual and combined concentrations of drugs that achieved certain cells growth/death were determined using a sulforhodamine B(SRB) assay. Drug effects on cell viability were further confirmed using floating cell count and trypan blue exclusion assay. The mean Values ± standard deviation were calculated and compared between treatment groups using unpaired t test. Results: The concentration of paclitaxel alone that inhibited 50% of cell growth(IC50) was 0.5 μmol/L. This concentration increased to 1.2 μmol/L when paclitaxel was given in sequential combination with MSeA. The number of dead cells after the combination treatment did not show a significance increase when compared with drug alone. Conclusion:Pretreatment with MSeA did not enhance the paclitaxel effect against A2780 ovarian cancer cells. Objective:The role of methylseleninic acid (MSeA), a selenium compound, has been documented in cancer chemoprevention. However, the therapeutic effect of MSeA in combination with paclitaxel, a chemotherapeutic agent used to treat ovarian cancer, is unknown. In this study, we investigated the effect of combination treatment of MSeA and paclitaxel against ovarian cancer cells. Methods:Ovarian cancer cells(A2780) were treated with different concentrations of MSeA, paclitaxel alone or in combination. The individual and combined concentrations of drugs that achieved certain cells growth/death were determined using a sulforhodamine B(SRB) assay. Drug effects on cell viability were further confirmed using floating cell count and trypan blue exclusion assay. The mean Values ± standard deviation were calculated and compared between treatment groups using unpaired t test. Results: The concentration of paclitaxel alone that inhibited 50% of cell growth(IC50) was 0.5 μmol/L. This concentration increased to 1.2 μmol/L when paclitaxel was given in sequential combination with MSeA. The number of dead cells after the combination treatment did not show a significance increase when compared with drug alone. Conclusion:Pretreatment with MSeA did not enhance the paclitaxel effect against A2780 ovarian cancer cells.
出处 《Journal of Nanjing Medical University》 2009年第2期111-116,共6页 南京医科大学学报(英文版)
基金 supported in part by a research grant form the American Cancer Society(IRG0219706) a comprehensive cancer center support grant from the National Cancer Institute(CA016056)
关键词 methylseleninic acid PACLITAXEL ovarian cancer methylseleninic acid paclitaxel ovarian cancer
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  • 1Snyder JP,Nettles JH,Cornett B,Downing KH,Nogales E.The binding conformation of paclitaxel in beta-tubulin:a model based on electron crystallographic density[].Proceedings of the National Academy of Sciences of the United States of America.2001
  • 2Morris JDH,Pramanik R,Zhang X,Carey AM,Ragavan N,Martin FL,et al.Selenium-or quercetin-induced retardation of DNA synthesis in primary prostate cells occurs in the presence of a concomitant reduction in androgen-receptor activity[].Cancer Letters.2006
  • 3Kondo S,Barnett G H,Hara H,et al.MDM2 protein confers the resistance of a human glioblastoma cell line to cisplatin-induced apoptosis[].Oncegene.1995
  • 4Rowinsky E K.The development and clinical utility of the taxane class of antimicrotubule chemotherapy agents[].Annual Review of Medicine.1997
  • 5Combs G F,Gray W P.Chemopreventive agents: selenium[].Pharmacology and Therapeutics.1998
  • 6Soussi T,Lozano G.p53 mutation heterogeneity in cancer[].Biochemical and Biophysical Research Communications.2005
  • 7Ruo-Ran Mi and Hong Ni Ph.D.MDM2 sensitizes a human ovarian cancer cell line[].Gynecologic Oncology.2003
  • 8Jemal,A,Siegel,R,Ward,E,Murray,T,Xu,J,Thun,MJ.Cancer statistics 2007, CA: a[].CA A Cancer Journal for Clinicians.2007
  • 9Alan H DeCherney,Lauren Nathan.Current Obstetric&Gynecologic Diagnosis&Treat-ment[]..2003
  • 10Ozols,RF,Bundy,BN,Greer,BE,Fowler,JM,Clarke-Pearson,D,Burger,RA,Mannel,RS,DeGeest,K,Hartenbach,EM,Baergen,R.Phase III trial of carboplatin and paclitaxel compared with cisplatin and pacltitaxel in patients with optimally resected stage III ovarian cancer: a Gynecologic Oncology Group study[].Journal of Clinical Oncology.2003

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