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首页> 外文期刊>BMC Complementary and Alternative Medicine >Jingfukang induces anti-cancer activity through oxidative stress-mediated DNA damage in circulating human lung cancer cells
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Jingfukang induces anti-cancer activity through oxidative stress-mediated DNA damage in circulating human lung cancer cells

机译:精复康通过氧化应激介导的循环性肺癌细胞中的DNA损伤诱导抗癌活性

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Metastasis is the main cause of lung cancer death. As a seed of metastasis, circulating tumor cells are an important target for metastasis intervention. The traditional Chinese medicine, Jinfukang, has been clinically available for the treatment of non-small cell lung cancer (NSCLC). In this study, we investigated the action and underlying mechanisms of Jinfukang against circulating lung tumor cells. The cell counting kit-8 (CCK-8), colony formation and cell cycle assays were used to study the cell proliferation ability. Flow cytometry was used to detect the apoptosis and the expression level of ROS and Caspase-3. Comet and TUNEL assays were used to detect DNA damage. DNA damage related pathway protein was detected by western blot. Jinfukang significantly inhibits the proliferation of CTC-TJH-01 cells by inducing G1 phase arrest and inhibits their colony formation in a dose-dependent manner. Moreover, Jinfukang induces apoptosis in CTC-TJH-01 cells through the ROS-mediated ATM/ATR-p53 pathway and DNA damage. Our findings suggest that Jinfukang may be a potential drug for lung cancer metastasis.
机译:转移是肺癌死亡的主要原因。作为转移的种子,循环中的肿瘤细胞是转移干预的重要靶标。传统中药金复康已在临床上用于治疗非小细胞肺癌(NSCLC)。在这项研究中,我们研究了金复康对循环肺肿瘤细胞的作用及其潜在机制。使用细胞计数试剂盒8(CCK-8),集落形成和细胞周期测定来研究细胞增殖能力。流式细胞仪检测细胞凋亡及ROS和Caspase-3的表达。使用彗星和TUNEL分析检测DNA损伤。通过western blot检测DNA损伤相关途径蛋白。金复康通过诱导G1期阻滞而显着抑制CTC-TJH-01细胞的增殖,并以剂量​​依赖的方式抑制其集落形成。此外,金复康通过ROS介导的ATM / ATR-p53途径和DNA损伤诱导CTC-TJH-01细胞凋亡。我们的发现表明,金复康可能是肺癌转移的潜在药物。

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