The epigenetically-regulated miR-663 targets H-ras in K-562 cells

被引:20
作者
Yang, Yang [1 ,2 ,3 ]
Wang, Li-Li [1 ,2 ]
Wang, Heng-Xiang [3 ]
Guo, Zi-Kuan [4 ]
Gao, Xiao-Fang [5 ]
Cen, Jian [6 ]
Li, Yong-Hui [1 ,2 ]
Dou, Li-Ping [1 ,2 ]
Yu, Li [1 ,2 ]
机构
[1] Chinese Peoples Liberat Army Gen Hosp, Dept Haematol, Beijing, Peoples R China
[2] Chinese Peoples Liberat Army Gen Hosp, BMT Ctr, Beijing, Peoples R China
[3] Chinese PLA AF Gen Hosp, Dept Haematol, Beijing, Peoples R China
[4] Beijing Inst Radiat Med, Beijing, Peoples R China
[5] Chinese Peoples Liberat Army Gen Hosp, Dept Respirat, Beijing, Peoples R China
[6] Chinese PLA Navy Gen Hosp, Dept Haematol, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
DNA methylation; epigenetics; gene expression; H-ras; MiR-663; TUMOR-SUPPRESSOR; MICRORNAS; CANCER; GENE; KRAS; TUMORIGENESIS; METHYLATION; EXPRESSION; PATHWAY;
D O I
10.1111/febs.12485
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
miR-663 is a tumour suppressor that is potentially regulated by modification of CpG islands. Whether aberrant methylation is one of the reasons for miR-663 down-regulation in some malignant cells and whether miR-663 targets oncogenes warrants further research. In the present study, we report that the CpG islands in the upstream region of pre-miR-663 are aberrantly methylated in the k-562 cell line and in the white blood cells of some chronic myelogenous leukaemia patients, and also that H-ras is one of the genes targeted by miR-663. Over-expression of miR-663 may suppress proliferation of the k-562 cell line in part by enhancing cell apoptosis.
引用
收藏
页码:5109 / 5117
页数:9
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