首页> 美国卫生研究院文献>Wiley-Blackwell Online Open >Anemarrhena asphodeloides Bunge and its constituent timosaponin‐AIII induce cell cycle arrest and apoptosis in pancreatic cancer cells
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Anemarrhena asphodeloides Bunge and its constituent timosaponin‐AIII induce cell cycle arrest and apoptosis in pancreatic cancer cells

机译:知母二倍体及其成分timosaponin-AIII诱导胰腺癌细胞的细胞周期阻滞和凋亡

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摘要

Pancreatic cancer is one of the most recalcitrant and lethal of all cancers. We examined the effects of Anemarrhena asphodeloides (AA) and timosaponin‐AIII (TAIII), a steroidal saponin present in AA, on pancreatic cancer cell proliferation and aimed to elucidate their potential apoptotic mechanisms of action. Viability assays and cell cycle analysis revealed that both AA and TAIII significantly inhibited pancreatic cancer cell proliferation and cell cycle progression compared to treatment with gemcitabine, the standard chemotherapeutic agent for advanced pancreatic cancer. We identified a dose‐dependent increase in caspase‐dependent apoptosis and activation of pro‐apoptotic PI3K/Akt pathway proteins, with a subsequent downregulation of pro‐survival PI3K/Akt pathway proteins, in pancreatic cancer cells treated with AA or TAIII over those treated with gemcitabine.
机译:胰腺癌是所有癌症中最顽强和致命的癌症之一。我们检查了知母二倍体(AA)和timosaponin-AIII(TAIII)(一种存在于AA中的甾体皂苷)对胰腺癌细胞增殖的作用,旨在阐明其潜在的凋亡机制。生存力分析和细胞周期分析表明,与吉西他滨(一种用于晚期胰腺癌的标准化学治疗剂)相比,AA和TAIII均能显着抑制胰腺癌细胞的增殖和细胞周期进程。我们发现,用AA或TAIII治疗的胰腺癌细胞中caspase依赖性凋亡和促凋亡PI3K / Akt途径蛋白激活的剂量依赖性增加,以及随后的存活PI3K / Akt途径蛋白的下调。与吉西他滨。

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