| Literature DB >> 29414759 |
Edmond Changkyun Park1,2,3, Jae Sung Lim4, Seung Il Kim1,2,3, Sang-Yeop Lee1,2, Yu-Kyung Tak1, Chi-Won Choi1,5, Sungho Yun1, Joohyun Park1, Minji Lee1,3, Hyo Kyun Chung6, Koon Soon Kim6, Yong Gil Na4, Ju Hyun Shin4, Gun-Hwa Kim7,3,5.
Abstract
Overactive bladder (OAB) syndrome is a condition that has four symptoms: urgency, urinary frequency, nocturia, and urge incontinence and negatively affects a patient's life. Recently, it is considered that the urinary bladder urothelium is closely linked to pathogenesis of OAB. However, the mechanisms of pathogenesis of OAB at the molecular level remain poorly understood, mainly because of lack of modern molecular analysis. The goal of this study is to identify a potential target protein that could act as a predictive factor for effective diagnosis and aid in the development of therapeutic strategies for the treatment of OAB syndrome. We produced OAB in a rat model and performed the first proteomic analysis on the mucosal layer (urothelium) of the bladders of sham control and OAB rats. The resulting data revealed the differential expression of 355 proteins in the bladder urothelium of OAB rats compared with sham subjects. Signaling pathway analysis revealed that the differentially expressed proteins were mainly involved in the inflammatory response and apoptosis. Our findings suggest a new target for accurate diagnosis of OAB that can provide essential information for the development of drug treatment strategies as well as establish criteria for screening patients in the clinical environment.Entities:
Mesh:
Substances:
Year: 2018 PMID: 29414759 PMCID: PMC5930411 DOI: 10.1074/mcp.RA117.000290
Source DB: PubMed Journal: Mol Cell Proteomics ISSN: 1535-9476 Impact factor: 5.911