...
首页> 外文期刊>Oncology letters >Regulatory roles of microRNA-708 and microRNA-31 in proliferation, apoptosis and invasion of colorectal cancer cells.
【24h】

Regulatory roles of microRNA-708 and microRNA-31 in proliferation, apoptosis and invasion of colorectal cancer cells.

机译:microRNA-708和microRNA-31在大肠癌细胞增殖,凋亡和侵袭中的调控作用。

获取原文
获取原文并翻译 | 示例
           

摘要

MicroRNAs (miRs) function as key regulators of gene expression and their deregulation is associated with the carcinogenesis of various cancers. In the present study, the aim was to validate the potential roles and regulatory mechanisms of miR-708 and miR-31 in colorectal cancer (CRC) cells. miR-708 and miR-31 were found to be highly expressed in five CRC tissue samples. Functional studies showed that the inhibition of miR-708 and miR-31 inhibited cell proliferation and invasion, however, promoted apoptosis in vitro. Subsequently, it was identified that miR-708 and miR-31 directly target cyclin-dependent kinase inhibitor 2B (CDKN2B) by binding to the 3' untranslated region, which suppresses the CDKN2B protein levels. In addition, the CDKN2B protein levels were significantly reduced when there was high miR-708 and miR-31 expression in the CRC tissue samples. The results indicate that miR-31 and miR-708 function in an oncogenic manner in CRC development, and inhibition of the two miRs may be used as a therapeutic strategy for patients with CRC.
机译:微小RNA(miR)充当基因表达的关键调节剂,其失调与各种癌症的致癌作用有关。在本研究中,目的是验证miR-708和miR-31在结直肠癌(CRC)细胞中的潜在作用和调节机制。发现miR-708和miR-31在五个CRC组织样本中高表达。功能研究表明,对miR-708和miR-31的抑制作用抑制了细胞的增殖和侵袭,但在体外促进了细胞凋亡。随后,已确定miR-708和miR-31通过与3'非翻译区结合而直接靶向细胞周期蛋白依赖性激酶抑制剂2B(CDKN2B),从而抑制CDKN2B蛋白水平。此外,当CRC组织样品中高miR-708和miR-31表达时,CDKN2B蛋白水平显着降低。结果表明,miR-31和miR-708在致癌过程中以致癌方式发挥作用,并且抑制这两种miR可用作CRC患者的治疗策略。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号