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Inhibitory effect of (?)-epigallocatechin-3-gallate and bleomycin on human pancreatic cancer MiaPaca-2 cell growth

机译:(?)-表没食子儿茶素-3-没食子酸酯和博来霉素对人胰腺癌MiaPaca-2细胞生长的抑制作用

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Background Human pancreatic cancer is currently one of the deadliest cancers with high mortality rate. It has been previously shown that (?)-epigallocatechin-3-gallate (EGCG), the most abundant catechin found in green tea, has showed suppressive effects on human pancreatic cancer cells. Bleomycin, (BLM), an anti-cancer chemotherapeutic drug that induces DNA damage, has antitumor effects by induction of apoptosis in several cancer cell lines and also in pancreatic cancer cells. The present study investigated for the first time, the inhibitory effect of EGCG and BLM on pancreatic cancer cell growth. Methods Using the pancreatic cancer cell lines MIA PaCa-2 cells the efficacy and synergism of EGCG and BLM were evaluated by in vitro tests. Inhibition of cell proliferation was determined by MTT assay. Mitochondrial depolarization was performed with JC-1 probe. Viability and apoptosis were determined by Flow Cytometry with annexin V, propidium iodide staining and DNA fragmentation assay. Results Cell proliferation assay revealed significant additive inhibitory effects with combination of EGCG and BLM at 72 h in a dose dependent manner. The combination of EGCG and BLM induced cell cycle S-phase arrest and mitochondrial depolarization. Viability, apoptosis and DNA fragmentation assay indicated that the combination of EGCG and bleomycin potentiated apoptosis. Conclusions Our results indicate that EGCG and BLM have additive anti-proliferative effects in vitro by induction of apoptosis of MIA PaCa-2 cells. This combination could represent a new strategy with potential advantages for treatment of pancreatic cancer. To date, this is the first report published of the inhibitory effect of EGCG and BLM on human pancreatic cancer MIA Paca-2 cell growth.
机译:背景技术人类胰腺癌是目前死亡率最高的最致命的癌症之一。以前已经证明,(α)-表没食子儿茶素-3-没食子酸酯(EGCG)是绿茶中发现的最丰富的儿茶素,已经显示出对人胰腺癌细胞的抑制作用。博来霉素(BLM)是一种诱导DNA损伤的抗癌化学治疗药物,通过诱导几种癌细胞系以及胰腺癌细胞的凋亡而具有抗肿瘤作用。本研究首次研究了EGCG和BLM对胰腺癌细胞生长的抑制作用。方法使用胰腺癌细胞系MIA PaCa-2细胞通过体外试验评估EGCG和BLM的功效和协同作用。通过MTT分析确定细胞增殖的抑制。用JC-1探针进行线粒体去极化。通过膜联蛋白V的流式细胞术,碘化丙啶染色和DNA片段化测定来确定生存力和凋亡。结果细胞增殖试验显示,在72 h时,EGCG和BLM的组合具有明显的累加抑制作用,呈剂量依赖性。 EGCG和BLM的组合可诱导细胞周期S期阻滞和线粒体去极化。活力,凋亡和DNA片段化分析表明EGCG和博来霉素的组合增强了细胞凋亡。结论我们的结果表明EGCG和BLM通过诱导MIA PaCa-2细胞凋亡在体外具有累加的抗增殖作用。这种组合可能代表了一种具有治疗胰腺癌潜在优势的新策略。迄今为止,这是关于EGCG和BLM对人胰腺癌MIA Paca-2细胞生长的抑制作用的第一份报道。

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