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Cell proliferation and invasion ability of human choriocarcinoma cells lessened due to inhibition of Sox2 expression by microRNA-145

机译:由于microRNA-145抑制Sox2表达降低了人绒癌的细胞增殖和侵袭能力

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摘要

To date, the mechanism underlying the development of human choriocarcinomas has not been elucidated. It is hypothesized that the Sox2 protein plays a pivotal role in the proliferation and invasion capacity of tumor cells. A microRNA (miR-145) was cloned and used to study the expression of Sox2 and its regulatory effect on the proliferation and invasion capacity of the human choriocarcinoma cell line JAR. In the present study, Sox2 mRNA and protein expression decreased in JAR and JEG-3 cells following transfection with the miR-145 expression virus. Cell proliferation assays indicated that miR-145 expression affected cell cycle regulation and suppressed the proliferation of choriocarcinoma cells in vitro. In addition, xenograft experiments confirmed the suppression of tumor growth in vivo due to cell cycle arrest. Therefore, endogenous mature miR-145 expression may have an important role in the pathogenesis of human choriocarcinomas via interference with the Sox2 target gene by epigenetic modification. This information is of potential significance for the identification of therapeutic targets in human choriocarcinoma.
机译:迄今为止,尚未阐明人类绒毛膜癌发展的潜在机制。假设Sox2蛋白在肿瘤细胞的增殖和侵袭能力中起关键作用。克隆了微小RNA(miR-145),用于研究Sox2的表达及其对人绒毛膜癌细胞株JAR增殖和侵袭能力的调控作用。在本研究中,用miR-145表达病毒转染后,JAR和JEG-3细胞中Sox2 mRNA和蛋白表达降低。细胞增殖测定表明,miR-145的表达影响了细胞周期的调控,并在体外抑制了绒癌组织的增殖。另外,异种移植实验证实了由于细胞周期停滞而抑制了体内肿瘤的生长。因此,内源性成熟miR-145表达可能通过表观遗传修饰干扰Sox2靶基因而在人绒癌的发病中起重要作用。该信息对于鉴定人绒毛膜癌的治疗靶标具有潜在的意义。

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