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新型微小RNA-5582-5p通过直接靶向GAB1、SHC1和CDK2诱导癌细胞凋亡和细胞周期停滞,从而发挥肿瘤抑制作用。

Novel miR-5582-5p functions as a tumor suppressor by inducing apoptosis and cell cycle arrest in cancer cells through direct targeting of GAB1, SHC1, and CDK2.

作者信息

An Hyun-Ju, Kwak Seo-Young, Yoo Je-Ok, Kim Jae-Sung, Bae In-Hwa, Park Myung-Jin, Cho Mee-Yon, Kim Joon, Han Young-Hoon

机构信息

Division of Radiation Cancer Research, Korea Institute of Radiological and Medical Sciences, Nowon-gil 75, Nowon-gu, Seoul 139-706, Republic of Korea; Laboratory of Biochemistry, School of Life Sciences and Biotechnology, Korea University, Anam-ro 145, Seongbuk-gu, Seoul 136-701, Republic of Korea.

Division of Radiation Cancer Research, Korea Institute of Radiological and Medical Sciences, Nowon-gil 75, Nowon-gu, Seoul 139-706, Republic of Korea.

出版信息

Biochim Biophys Acta. 2016 Oct;1862(10):1926-37. doi: 10.1016/j.bbadis.2016.07.017. Epub 2016 Jul 28.

Abstract

MicroRNAs (miRNAs) play pivotal roles in tumorigenesis as either tumor suppressors or oncogenes. In the present study, we discovered and demonstrated the tumor suppressive function of a novel miRNA miR-5582-5p. miR-5582-5p induced apoptosis and cell cycle arrest in cancer cells, but not in normal cells. GAB1, SHC1, and CDK2 were identified as direct targets of miR-5582-5p. Knockdown of GAB1/SHC1 or CDK2 phenocopied the apoptotic or cell cycle arrest-inducing function of miR-5582-5p, respectively. The expression of miR-5582-5p was lower in tumor tissues than in adjacent normal tissues of colorectal cancer patients, while the expression of the target proteins exhibited patterns opposite to that of miR-5582-5p. Intratumoral injection of a miR-5582-5p mimic or induced expression of miR-5582-5p in tumor cells suppressed tumor growth in HCT116 xenografts. Collectively, our results suggest a novel tumor suppressive function for miR-5582-5p and its potential applicability for tumor control.

摘要

微小RNA(miRNA)作为肿瘤抑制因子或癌基因在肿瘤发生过程中发挥着关键作用。在本研究中,我们发现并证实了一种新型miRNA miR-5582-5p具有肿瘤抑制功能。miR-5582-5p可诱导癌细胞凋亡和细胞周期停滞,但对正常细胞无此作用。GAB1、SHC1和CDK2被确定为miR-5582-5p的直接靶点。敲低GAB1/SHC1或CDK2分别模拟了miR-5582-5p诱导凋亡或细胞周期停滞的功能。在结直肠癌患者中,肿瘤组织中miR-5582-5p的表达低于相邻正常组织,而靶蛋白的表达模式与miR-5582-5p相反。瘤内注射miR-5582-5p模拟物或诱导肿瘤细胞中miR-5582-5p表达可抑制HCT116异种移植瘤的生长。总体而言,我们的结果表明miR-5582-5p具有新型肿瘤抑制功能及其在肿瘤控制中的潜在应用价值。

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