| Literature DB >> 35311447 |
Yuan Chen1, Shiben Ji2, Jianxin Ying2, Yongchang Sun2, Jun Liu2, Guohong Yin2.
Abstract
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.Entities:
Keywords: KRT6A; RNA-seq; apoptosis; bladder cancer; miR-31-5p; proliferation
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Year: 2022 PMID: 35311447 PMCID: PMC9278449 DOI: 10.1080/15384101.2022.2054095
Source DB: PubMed Journal: Cell Cycle ISSN: 1551-4005 Impact factor: 5.173