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