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Molecular mechanism of extracellular matrix disorder in pelvic organ prolapses

Pelvic organ prolapses (POP) notably reduces the quality of life in elderly populations due to bladder and bowel dysfunction, incontinence, and coital problems. Extracellular matrix (ECM) disorder is a pivotal event in the progression of POP, but to date, its specific underlying mechanism remains un...

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Detalles Bibliográficos
Autores principales: Zhang, Liping, Dai, Fangfang, Chen, Gantao, Wang, Yanqing, Liu, Shiyi, Zhang, Li, Xian, Shu, Yuan, Mengqin, Yang, Dongyong, Zheng, Yajing, Deng, Zhimin, Cheng, Yanxiang, Yang, Xiaofeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7646844/
https://www.ncbi.nlm.nih.gov/pubmed/33173982
http://dx.doi.org/10.3892/mmr.2020.11564
Descripción
Sumario:Pelvic organ prolapses (POP) notably reduces the quality of life in elderly populations due to bladder and bowel dysfunction, incontinence, and coital problems. Extracellular matrix (ECM) disorder is a pivotal event in the progression of POP, but to date, its specific underlying mechanism remains unclear. The ligaments of patients with POP and healthy controls were collected to compare the expression of Homeobox11 (HOXA11) and transforming growth factor β (TGF-β1) via immunohistochemical analysis. HOXA11 and TGF-β1 were overexpressed or knocked down in fibroblast cells to explore their effects on the expression of collagen and matrix metalloproteinases (MMPs). HOXA11 and TGF-β1 were greatly reduced in the ligaments of patients with POP. The overexpression and downregulation of HOXA11 and TGF-β1 can mediate ECM disorder via regulating expression of collagen (Col) and MMPs. In addition, HOXA11 and TGF-β1 exerted synergistic effect on the expression of Col and MMPs. The present study identified that HOXA11 and TGF-β1 serve critical roles in mediating ECM disorders, which may be of clinical significance for the diagnosis and treatment of patients with POP.