KRT6A expedites bladder cancer progression, regulated by miR-31-5p

Chen Yuan; Ji Shiben; Ying JianxinSun YongchangLiu JunYin Guohong

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KRT6A expedites bladder cancer progression, regulated by miR-31-5p

机译：KRT6A expedites bladder cancer progression, regulated by miR-31-5p

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摘要

Bladder cancer is one of the most severe life-threatening illnesses worldwide. To contribute to a solution to this public health issue, here, we sought to identify a novel biomarker for the early diagnosis of bladder tumors. We conducted RNA sequence analysis utilizing samples from tumorous tissue and adjacent healthy tissue in bladder cancer patients and found that KRT6A was upregulated in bladder tumor tissues, suggesting that it might be a candidate for involvement in bladder tumorigenesis. Accordingly, we performed a series of experiments to further verify the role of KRT6A in bladder tumor progression. Our results revealed that KRT6A promoted bladder tumor cell viability, proliferation, and adhesion, while diminishing bladder tumor cell apoptosis. We also focused on the role of epigenetics in bladder tumors and verified that KRT6A was a miR-31-5p target gene, and its positive effect on bladder tumor progression was relieved by miR-31-5p. Overall, this study sheds new light regarding a novel oncogenic regulatory axis, KRT6A/miR-31-5p, which is related to bladder tumor growth.

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《Cell cycle》 |2022年第14期|1479-1490|共12页
作者
Chen Yuan; Ji Shiben; Ying JianxinSun YongchangLiu JunYin Guohong;
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作者单位

Tongji Hosp,Huazhong Univ Sci & Technol;

Dept Urol,Wuhan Hankou Hosp;

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原文格式 PDF
正文语种英语
中图分类细胞生物学;
关键词
RNA-seq; KRT6A; bladder cancer; miR-31-5p; apoptosis; proliferation; GENES; DIFFERENTIATION; IDENTIFICATION; REPRESSION; EXPRESSION; CELLS;

KRT6A expedites bladder cancer progression, regulated by miR-31-5p

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