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微小RNA-21促进HeLa宫颈癌细胞的增殖并下调程序性细胞死亡4(PDCD4)的表达。

MicroRNA-21 promotes cell proliferation and down-regulates the expression of programmed cell death 4 (PDCD4) in HeLa cervical carcinoma cells.

作者信息

Yao Qing, Xu Hui, Zhang Qian-Qian, Zhou Hui, Qu Liang-Hu

机构信息

Key Laboratory of Gene Engineering of the Ministry of Education, State Key Laboratory for Biocontrol, Sun Yat-Sen University, Guangzhou 510275, PR China.

出版信息

Biochem Biophys Res Commun. 2009 Oct 23;388(3):539-42. doi: 10.1016/j.bbrc.2009.08.044. Epub 2009 Aug 12.

Abstract

MicroRNAs are involved in cancer-related processes. The microRNA-21(miR-21) has been identified as the only miRNA over-expressed in a wide variety of cancers, including cervical cancer. However, the function of miR-21 is unknown in cervical carcinomas. In this study, we found that the inhibition of miR-21 in HeLa cervical cancer cells caused profound suppression of cell proliferation, and up-regulated the expression of the tumor suppressor gene PDCD4. We also provide direct evidence that PDCD4-3'UTR is a functional target of miR-21 and that the 18bp putative target site can function as the sole regulatory element in HeLa cells. These results suggest that miR-21 may play an oncogenic role in the cellular processes of cervical cancer and may serve as a target for effective therapies.

摘要

微小RNA参与癌症相关过程。微小RNA - 21(miR - 21)已被确定为在包括宫颈癌在内的多种癌症中唯一过度表达的微小RNA。然而,miR - 21在宫颈癌中的功能尚不清楚。在本研究中,我们发现抑制HeLa宫颈癌细胞中的miR - 21会导致细胞增殖受到显著抑制,并上调肿瘤抑制基因PDCD4的表达。我们还提供了直接证据,证明PDCD4 - 3'UTR是miR - 21的功能性靶点,并且18bp的假定靶位点可作为HeLa细胞中的唯一调控元件发挥作用。这些结果表明,miR - 21可能在宫颈癌的细胞过程中发挥致癌作用,并可能成为有效治疗的靶点。

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