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hsa-miR-96 up-regulates MAP4K1 and IRS1 and may function as a promising diagnostic marker in human bladder urothelial carcinomas

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成果类型:
期刊论文
作者:
Wang, Yi;Luo, Hongmei;Li, Yangle;Chen, Tieding;Wu, Shengpeng;...
通讯作者:
Yang, Luoyan
作者机构:
[Wang, Yi; Chen, Tieding; Yang, Luoyan; Wu, Shengpeng; Li, Yangle] Cent S Univ, Xiangya Hosp 2, Dept Urol, Changsha 410011, Hunan, Peoples R China.
[Luo, Hongmei] Univ S China, Dept Histol & Embryol, Hengyang 421001, Hunan, Peoples R China.
通讯机构:
[Yang, Luoyan] C
Cent S Univ, Xiangya Hosp 2, Dept Urol, Changsha 410011, Hunan, Peoples R China.
语种:
英文
关键词:
hsa-miR-96;diagnostic marker;MAP4K1;insulin receptor substrate 1
期刊:
MOLECULAR MEDICINE REPORTS
ISSN:
1791-2997
年:
2012
卷:
5
期:
1
页码:
260-265
基金类别:
Educational Commission Fund of Hunan Province in China [10C1164]
机构署名:
本校为其他机构
院系归属:
医学院
摘要:
Numerous microRNAs (miRNAs) play crucial roles in cancer development. In this study, we report that hsa-miR-96 is expressed at higher levels in human bladder urothelial carcinomas compared to normal tissues. We found that hsa-miR-96 increased invasion and differentiation of human bladder T24 cells and promoted their growth. Downregulation of hsa-miR-96 significantly affected the phenotype of bladder cancer T24 cells. The mRNA and protein levels of insulin receptor substrate 1 (IRS1) and MAP4K1 were significantly reduced in cells transfected with the hsa-miR-96 inhibitor when compared with leve...

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