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首页> 外文期刊>Journal of cellular and molecular medicine. >CircPRMT5 circular RNA promotes proliferation of colorectal cancer through sponging miR‐377 to induce E2F3 expression
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CircPRMT5 circular RNA promotes proliferation of colorectal cancer through sponging miR‐377 to induce E2F3 expression

机译:循环循环RNA通过海绵miR-377促进结直肠癌的增殖,诱导E2F3表达

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CircPRTM5 is associated with cell proliferation and migration in many kinds of malignancies. However, the functions and mechanisms of CircPRTM5 in CRC progression remain unclear. We explored the role and the mechanisms of CircPRTM5 in the development of CRC. Tissues of CRC patients and matched adjacent non‐tumour tissues were collected to evaluate the expression of CircPRTM5. The expression of CircPRTM5 in CRC tissues was significantly higher than that in adjacent tissues. The biological functions of CircPRTM5 in CRC were determined by overexpression and down‐regulation of CircPRTM5 in CRC cells in vitro and in vivo. The results indicate that knockdown of CircPRTM5 can significantly inhibit the proliferation of CRC cells. The potential mechanisms of CircPRTM5 in CRC development were identified by RT‐qPCR, Western blotting analysis and luciferase reporter assay. CircPRTM5 competitively regulates the expression of E2F3 by capillary adsorption of miR‐377. CircPRMT5 regulates CRC proliferation by regulating the expression of E2F3, which affects the expression of the cell cycle‐associated proteins cyclinD1 and CDK2. CircPRTM5 exerts critical regulatory role in CRC progression by sponging miR‐377 to induce E2F3 expression.
机译:CircPrtm5与多种恶性肿瘤中的细胞增殖和迁移有关。但是,CRC进展中的CIRCPRTM5的功能和机制仍然不清楚。我们探讨了CRC发展中CIRCPRTM5的作用和机制。收集CRC患者的组织和相邻的非肿瘤组织匹配,评估循环循环株的表达。 CRC组织中循环循环组织的表达明显高于相邻组织中的表达。 CRC中循环循环方法的生物学功能是通过在体外和体内在CRC细胞中的过表达和下调CRICPRTM5测定。结果表明,CircPrtm5的敲低可以显着抑制CRC细胞的增殖。通过RT-QPCR,Western印迹分析和Luciferase报道分析确定CRC开发中的潜在机制。 CircPRTM5竞争性地通过MiR-377的毛细管吸附来调节E2F3的表达。 CircPRMT5通过调节E2F3的表达来调节CRC增殖,这影响细胞周期相关蛋白质环壁1和CDK2的表达。 CircPRTM5通过海绵MIR-377诱导E2F3表达对CRC进展中的临界监管作用。

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