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TCM matrine inducescell arrest and apoptosis with recovery expression of the hepato-specific miR122a in human hepatocellular carcinomaHep G2cell line

机译:中药苦参碱诱导人肝细胞癌Hep G2细胞株中肝特异性miR122a的恢复表达并诱导细胞停滞和凋亡

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摘要

Hepatocellular carcinoma (HCC) accounts for 80% to 90% of liver cancers and it is one of the most prevalent carcinomas throughout the world. Traditional chemotherapy is often developed chemoresistance HCC patients.Matrine is an active component oftraditional Chinese medicine (TCM) and is a promising alternative HCC drug. In this study, the therapeutic effects and the underlying molecular mechanisms of matrine on the human HCC cell lineHep G2 were investigated. High dosage of matrine (1.0 mg/mL) could significantly (P < 0.05) inhibit cell proliferation by 48.39 ± 3.32%, under which cell shrinkage and disruption were observed. Flow cytometry assay showed that the proportion of G1/G0 cells significantly increased, while that of S and G2/M cells significantly decreased after treatment of matrinefor 48 h. These results indicated that cell arrest by matrine appeared. Up-regulation of the hepato-specific miR122a followed by down expression of its targetcyclin G1 (CG1) gene by low concentration of matrine (0.2 mg/mL) was detected using was observed using quantitative real-time PCR, immunohistochemistry (IHC) and western blot assays. In conclusion, matrineinducescell arrest and apoptosis with recovery expression of the hepato-specific miR122a in human hepatocellular carcinoma Hep G2 cell line.
机译:肝细胞癌(HCC)占肝癌的80%至90%,它是全世界最普遍的癌症之一。传统的化学疗法通常是发展为化学抗性的HCC患者。苦参碱是中药(TCM)的有效成分,是一种有希望的替代HCC药物。在这项研究中,研究了苦参碱对人HCC细胞株Hep G2的治疗作用及其潜在的分子机制。高剂量苦参碱(1.0 mg / mL)可以显着(P <0.05)抑制细胞增殖,达48.39±3.32%,在此下可观察到细胞萎缩和破坏。流式细胞仪检测苦参碱处理48h后G1 / G0细胞比例明显增加,而S和G2 / M细胞比例明显降低。这些结果表明出现了苦参碱引起的细胞停滞。使用定量实时荧光定量PCR,免疫组织化学(IHC)和Western观察到低浓度苦参碱(0.2 mg / mL)检测到肝特异性miR122a上调,然后下调了其靶环蛋白G1(CG1)基因的表达。印迹分析。总之,苦参碱在人肝细胞癌Hep G2细胞系中以肝特异性miR122a的恢复表达诱导细胞停滞和凋亡。

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