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Up-regulation of p16 by miR-877-3p inhibits proliferation of bladder cancer

Despite the recent studies which have shown that microRNA (miRNA) negatively regulates gene expression by silencing the expression of target genes, here we reported the new evidence of microRNA-mediated gene activation by targeting specific promoter sites. We identified a miR-877-3p binding site on...

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Detalles Bibliográficos
Autores principales: Li, Shiqi, Zhu, Yi, Liang, Zhen, Wang, Xiao, Meng, Shuai, Xu, Xin, Xu, Xianglai, Wu, Jian, Ji, Alin, Hu, Zhenghui, Lin, Yiwei, Chen, Hong, Mao, Yeqing, Wang, Wei, Zheng, Xiangyi, Liu, Ben, Xie, Liping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5239514/
https://www.ncbi.nlm.nih.gov/pubmed/27429046
http://dx.doi.org/10.18632/oncotarget.10575
Descripción
Sumario:Despite the recent studies which have shown that microRNA (miRNA) negatively regulates gene expression by silencing the expression of target genes, here we reported the new evidence of microRNA-mediated gene activation by targeting specific promoter sites. We identified a miR-877-3p binding site on the promoter site of tumor suppressor gene p16 which alters frequently in bladder cancer. Enforced expression of miR-877-3p could increase the expression of p16, which inhibit the proliferation and tumorigenicity of bladder cancer through cell cycle G1-phase arrest. Further evidences confirmed that the correlation between p16 activation and miR-877-3p was due to the direct binding. These findings demonstrate the anti-tumor function of miR-877-3p in bladder cancer cells and reveal a new pattern of miRNA involved gene regulation.