国际妇产科学杂志 ›› 2026, Vol. 53 ›› Issue (4): 412-417.doi: 10.12280/gjfckx.20260085

• 普通妇科疾病及相关研究:综述 • 上一篇    下一篇

细胞外基质代谢失衡在盆腔器官脱垂中的作用机制与治疗前景

林康, 马霞   

  1. 317000 浙江省台州医院妇产科
  • 收稿日期:2026-02-03 出版日期:2026-08-15 发布日期:2026-08-25

Mechanisms and Therapeutic Prospects of Extracellular Matrix Metabolic Imbalance in Pelvic Organ Prolapse

LIN Kang, MA Xia   

  1. Department of Obstetrics and Gynecology, Taizhou Hospital of Zhejiang Province, Taizhou 317000, Zhejiang Province, China
  • Received:2026-02-03 Published:2026-08-15 Online:2026-08-25

摘要:

盆腔器官脱垂(pelvic organ prolapse,POP)是一种常见的盆底功能障碍性疾病,其核心病理生理基础是细胞外基质(extracellular matrix,ECM)代谢的稳态失衡。该过程并非被动的组织退化,而是由多因素驱动、多细胞参与的主动重塑紊乱,表现为ECM合成与降解的动态平衡破坏。当前以手术为主的治疗方式存在复发率高等局限,因此,针对ECM代谢失衡本质的新型诊疗策略成为研究重点,包括靶向药物、再生疗法及组织工程等前沿方向。推动这些策略从基础向临床转化,必须依靠基础医学、生物材料学和临床医学的深度融合与协作,最终实现POP治疗从解剖复位向生物学功能重建的范式转变。

关键词: 盆腔器官脱垂, 细胞外基质, 基质金属蛋白酶类, 成纤维细胞, 组织工程

Abstract:

Pelvic organ prolapse (POP) is a common pelvic floor dysfunction disease, whose core pathophysiological basis is the homeostatic imbalance of extracellular matrix (ECM) metabolism. This process is not a passive tissue degeneration but an active remodeling disorder driven by multiple factors and involving multiple cell types, manifested as the disruption of the dynamic balance between ECM synthesis and degradation. Current treatment modalities, primarily surgical, face limitations such as a high recurrence rate. Therefore, novel diagnostic and therapeutic strategies targeting the essence of ECM metabolic imbalance have become a research focus, including cutting-edge directions such as targeted drugs, regenerative therapies, and tissue engineering. To facilitate the translation of these strategies from basic research to clinical application, deep integration and collaboration among basic medical science, biomaterials science, and clinical medicine are imperative. This ultimately aims to achieve a paradigm shift in POP treatment, moving from anatomical repositioning to the reconstruction of biological function.

Key words: Pelvic organ prolapse, Extracellular matrix, Matrix metalloproteinases, Fibroblasts, Tissue engineering