In vitro cytotoxicity perspective of diazepinomicin (ECO-4601) on human hepatoma cell line (HEPG2)

Vinayagam Rambabu, Subramaniyan Vijayakumar
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引用次数: 12

Abstract

Hepatocellular carcinoma is the leading cause of death and its incidence is rising year by year. There are numerous antioxidants available in various sources, including microorganisms. We had an attempt on validating the effect of diazepinomicin from Micromonospora strain against human hepatoma cell line (HepG2). Trypan blue exclusion assay was performed to determine the dead cells. Propidium iodide and Hoechst staining was performed to determine the apoptotic bodies. DNA fragmentation was performed on agarose gel electrophoresis and the expression of BAX and Bcl2 proteins were determined. Trypan blue exclusion assay showed dose-dependent cell death. Propidium iodide and Hoechst staining showed apoptotic bodies. DNA fragments were seen in both diazepinomicin 10 and 15 μM/mL treated Hep G2 cells. Western blot assay showed low intensity bands in diazepinomicin 10 and 15 μM/mL treated Hep G2 cells. Thus, the downregulation of these protein expressions reveal that the diazepinomicin has the ability to induce apoptosis. From all the parameters, it could be concluded that the diazepinomicin has anticancer potency against human hepatoma cell line (HepG2).

地氮西米星(ECO-4601)对人肝癌细胞株HEPG2的体外细胞毒性研究
肝细胞癌是人类死亡的主要原因,其发病率呈逐年上升趋势。抗氧化剂有多种来源,包括微生物。我们试图验证小单孢子菌重氮霉素对人肝癌细胞株(HepG2)的作用。台盼蓝排除法测定死亡细胞。采用碘化丙啶染色和Hoechst染色检测凋亡小体。琼脂糖凝胶电泳检测DNA片段,测定BAX和Bcl2蛋白的表达。台盼蓝排斥试验显示细胞死亡呈剂量依赖性。碘化丙啶染色和Hoechst染色显示凋亡小体。重氮霉素10 μM/mL和15 μM/mL处理的Hep G2细胞均可见DNA片段。Western blot检测显示,地氮平10和15 μM/mL处理的Hep G2细胞出现低强度条带。因此,这些蛋白表达的下调表明,地氮平霉素具有诱导细胞凋亡的能力。综上所述,地氮平霉素对人肝癌细胞株HepG2具有抗肿瘤作用。
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