Activation of Extrinsic Apoptotic Pathway From Bladder Biopsy in Patients With Interstitial Cystitis/Painful Bladder Syndrome

被引:20
作者
Lee, Jane-Dar
Lee, Ming-Huei
机构
[1] Taichung Armed Forces Gen Hosp, Div Urol, Dept Surg, Taichung, Taiwan
[2] Cent Taiwan Univ Sci & Technol, Taichung 42055, Taiwan
[3] Feng Yuan Hosp, Dept Urol, Dept Hlth, Taichung, Taiwan
关键词
CELL-DEATH; TNF-ALPHA; EXPRESSION; LIGAND; PATHOGENESIS; RECEPTOR-3; EPITHELIUM; ISCHEMIA; PROTEIN; TL1A;
D O I
10.1016/j.urology.2013.08.042
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE To investigate the intrinsic or extrinsic pathway of apoptosis from bladder biopsy that was performed in interstitial cystitis/painful bladder syndrome (IC/PBS). Although previous studies have reported observations of the dysfunction, denudation, and thinning of the bladder urothelium in patients associated with an increase of cell apoptosis, the molecular mechanism is unclear. METHODS The study group consisted of 32 patients with IC/PBS, and the control group consisted of 12 volunteers without any symptoms of IC. Bladder biopsies were obtained from both the groups. The expression of apoptosis-associated proteins was observed by detecting the Bcl-2/Bax ratio and the levels of cleaved caspase-9, Fas, cleaved caspase-8, and cleaved caspase-3 to differentiate intrinsic or extrinsic pathway. The data were analyzed using Mann-Whitney U test. RESULTS Increased levels of cleaved caspase-3 were found in the IC/PBS group relative to the control group (P < .05). The levels of the extrinsic apoptotic pathway proteins, Fas and cleaved caspase-8, were also increased in the study group compared with the control group (P < .05). There was no significant difference in the levels of the intrinsic apoptotic pathway proteins, including cleaved caspase-9 and the Bcl-2/Bax ratio, between the control and study groups. CONCLUSION Our findings demonstrate the activation of extrinsic apoptotic pathway from bladder biopsy in patients with IC/PBS. This study might help us to clarify the molecular changes and lead to a better understanding of this bladder disease. (C) 2013 Elsevier Inc.
引用
收藏
页码:1451.e7 / 1451.e11
页数:5
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