| Literature DB >> 25542424 |
Hui Deng1, Lei Lv1, Yang Li2, Cheng Zhang3, Fang Meng4, Youguang Pu1, Jun Xiao5, Liting Qian4, Weidong Zhao6, Qi Liu7, Daming Zhang8, Yingwei Wang9, Hongyu Zhang10, Yinghua He10, Jingde Zhu11.
Abstract
Chemoresistance prevents the curative cancer therapy, our understanding of which remains inadequate. Among the differentially expressed genes between the chemosensitive (5637) and chemoresistant (H-bc) bladder cancer cell lines, the expression level of the PSEN1 gene (presenilin 1), a key component of the γ-secretase, is negatively correlated with chemoresistance. A small interfering RNA mediated repression of the PSEN1 gene suppresses cell apoptosis and de-sensitizes 5637 cells, while overexpression of the presenilin 1 sensitizes H-bc cells to the drug-triggered cell death. As a direct target of microRNA-193a-3p that promotes the multi-chemoresistance of the bladder cancer cell, PSEN1 acts as an important executor for the microRNA-193a-3p's positive impact on the multi-chemoresistance of bladder cancer, probably via its activating effect on DNA damage response pathway. In addition to the mechanistic insights, the key players in this microRNA-193a-3p/PSEN1 axis are likely the diagnostic and/or therapeutic targets for an effective chemotherapy of bladder cancer.Entities:
Keywords: Bladder cancer; Chemoresistance; DNA damage response pathway; PSEN1; miR-193a-3p
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Year: 2014 PMID: 25542424 DOI: 10.1016/j.bbadis.2014.12.014
Source DB: PubMed Journal: Biochim Biophys Acta ISSN: 0006-3002