The State Engineering Laboratory of AIDS Vaccine, College of Life Science, Jilin University, Changchun, PR China.
Mol Med Rep. 2012 Mar;5(3):734-8. doi: 10.3892/mmr.2011.738. Epub 2011 Dec 23.
Pancreatic cancer is a highly malignant disease, with a 5-year survival rate of less than 4%. Thus, new therapies for this deadly disease are urgently required. In this study, we sought to investigate whether combination treatments with gemcitabine and clofarabine result in synergistic cytotoxic effects against human pancreatic cancer cells. The type and extent of cytotoxic interactions between gemcitabine and clofarabine in three human pancreatic cancer cell lines were determined by MTT assays and standard isobologram analysis. The effects of the two agents on cell cycle distribution and apoptosis were determined by flow cytometry. Clofarabine significantly and synergistically enhanced gemcitabine cytotoxicities in all of the cell lines tested. This was accompanied by a nearly complete S phase arrest and synergistic induction of apoptosis (cooperativity index = 0.67). Combined treatment of gemcitabine and clofarabine resulted in synergistic cytotoxicities in vitro. Our results strongly suggest potential clinical benefits for using this drug combination to treat pancreatic cancer patients.
胰腺癌是一种高度恶性的疾病,5 年生存率低于 4%。因此,迫切需要针对这种致命疾病的新疗法。在这项研究中,我们试图研究吉西他滨和克拉屈滨联合治疗是否对人胰腺癌细胞产生协同细胞毒性作用。通过 MTT 测定和标准等效应线分析确定吉西他滨和克拉屈滨在三种人胰腺癌细胞系中的细胞毒性相互作用的类型和程度。通过流式细胞术确定两种药物对细胞周期分布和凋亡的影响。克拉屈滨在所有测试的细胞系中均显著协同增强吉西他滨的细胞毒性。这伴随着几乎完全的 S 期阻滞和协同诱导凋亡(协同指数=0.67)。吉西他滨和克拉屈滨联合治疗在体外产生协同细胞毒性。我们的研究结果强烈表明,这种药物联合用于治疗胰腺癌患者具有潜在的临床获益。