Mitochondrial dysfunction in patients with urogenital disease

被引:4
作者
Chuang, Tzu-Yu [1 ]
Chang, Te-Wei [1 ]
Chen, Shiou-Sheng [1 ,2 ,3 ,4 ]
Chang, Chan-Chi [1 ]
Cheng, Wei-Ming [1 ,2 ]
Wei, Yau-Huei [5 ]
机构
[1] Taipei City Hosp, Div Urol, Zhongxiao Branch, Taipei, Taiwan
[2] Natl Yang Ming Chiao Tung Univ, Dept Urol, Sch Med, Taipei, Taiwan
[3] Natl Taiwan Univ Sci & Technol, Commiss Gen Educ, Taipei, Taiwan
[4] Univ Taipei, Gen Educ Ctr, Taipei, Taiwan
[5] Changhua Christian Hosp, Ctr Mitochondrial Med & Free Radical Res, 176,6th Floor,Zhonghua Rd, Changhua 50046, Taiwan
关键词
Bladder; mitochondria; urology; TRANSITIONAL-CELL CARCINOMA; URINARY-BLADDER; DNA MUTATIONS; OXIDATIVE DAMAGE; GENETIC-BASIS; CANCER; ASSOCIATION; REPAIR; RISK; 8-HYDROXY-2'-DEOXYGUANOSINE;
D O I
10.4103/UROS.UROS_47_21
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
Mitochondria are intracellular organelles responsible for the production of the majority of adenosine triphosphate (ATP). In addition to energy production, mitochondria also contribute to cellular apoptosis, the regulation of intracellular Ca2+ homeostasis, signaling through reactive oxygen species (ROS), and the coordination of the cell cycle. The prevalence rate of primary mitochondrial disease was estimated at nearly 1:5000. In this review, we have integrated recent evidence to discuss new insights into how mitochondrial dysregulation plays a role in bladder dysfunction, reproductive disorder and the correlation between mtDNA mutation and bladder cancer.
引用
收藏
页码:143 / 150
页数:8
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