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JAM-2表达在盆腔器官脱垂患者阴道壁组织中的临床意义

Clinical Significance of JAM-2 Expression in the Vaginal Wall Tissues of Patients With Pelvic Organ Prolapse.

作者信息

Liu Yuan, Mao Yajing, Wu Yuelin, Wan Sheng, Gu Shengyi, Peng Jing, Jiao Bo, Hua Xiaolin

机构信息

The International Peace Maternity & Child Health Hospital of China Welfare Institute (IPMCH), Shanghai Jiao Tong University School of Medicine, Shanghai, China.

Department of Obstetrics, Shanghai First Maternity and Infant Hospital, School of Medicine, Tongji University, Shanghai, China.

出版信息

J Cell Mol Med. 2025 Apr;29(7):e70512. doi: 10.1111/jcmm.70512.

DOI:10.1111/jcmm.70512
PMID:40159633
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11955420/
Abstract

This study aimed to elucidate the roles of junctional adhesion molecule 2 (JAM-2), collagen I and matrix metalloproteinase 2 (MMP-2) in the pathogenesis of pelvic organ prolapse (POP) and explore their potential as diagnostic markers. We examined 82 POP patients and 64 controls using enzyme-linked immunosorbent assay (ELISA) and quantitative Polymerase Chain Reaction (qPCR) to analyse protein and gene expression levels of JAM-2, Collagen I and MMP-2. Receiver operating characteristic (ROC) analysis evaluated their diagnostic efficacy, with correlation analyses linking molecular markers to POP severity based on POP-Q grades. Our study found no significant differences in age, BMI and vaginal parity between POP patients and controls. Molecular analyses revealed significant alterations in the expression levels of JAM-2, Collagen I and MMP-2 in POP patients. Specifically, there was a marked decrease in JAM-2 and collagen I levels, accompanied by an increase in MMP-2 expression, indicating a disruption in the balance between tissue synthesis and degradation. ROC analysis demonstrated the significant discriminative power of these markers, with substantial area under the curve (AUC) values for diagnosing POP. Correlation analysis further showed a significant association between the expression of JAM-2, Collagen I and MMP-2 and the clinical severity of POP, as indicated by POP-Q grades. Our findings revealed the significant changes in the expression of JAM-2, Collagen I and MMP-2 that may contribute to the POP pathogenesis. The diagnostic potential of these markers was substantiated, suggesting their utility in developing noninvasive diagnostic tools for POP.

摘要

本研究旨在阐明连接粘附分子2(JAM-2)、I型胶原蛋白和基质金属蛋白酶2(MMP-2)在盆腔器官脱垂(POP)发病机制中的作用,并探索它们作为诊断标志物的潜力。我们采用酶联免疫吸附测定(ELISA)和定量聚合酶链反应(qPCR)检测了82例POP患者和64例对照者,以分析JAM-2、I型胶原蛋白和MMP-2的蛋白质和基因表达水平。受试者工作特征(ROC)分析评估了它们的诊断效能,并基于POP-Q分期将分子标志物与POP严重程度进行相关性分析。我们的研究发现,POP患者与对照者在年龄、体重指数和阴道分娩次数方面无显著差异。分子分析显示,POP患者中JAM-2、I型胶原蛋白和MMP-2的表达水平有显著改变。具体而言,JAM-2和I型胶原蛋白水平显著降低,同时MMP-2表达增加,表明组织合成与降解之间的平衡被打破。ROC分析表明这些标志物具有显著的鉴别能力,诊断POP的曲线下面积(AUC)值较大。相关性分析进一步显示,JAM-2、I型胶原蛋白和MMP-2的表达与POP的临床严重程度(由POP-Q分期表示)之间存在显著关联。我们的研究结果揭示了JAM-2、I型胶原蛋白和MMP-2表达的显著变化,这些变化可能导致POP的发病机制。这些标志物的诊断潜力得到证实,表明它们在开发POP无创诊断工具方面具有实用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4a1/11955420/70e44c976d00/JCMM-29-e70512-g003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4a1/11955420/30664243a997/JCMM-29-e70512-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4a1/11955420/70e44c976d00/JCMM-29-e70512-g003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4a1/11955420/b9ec5b4974ac/JCMM-29-e70512-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4a1/11955420/30664243a997/JCMM-29-e70512-g001.jpg
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本文引用的文献

1
LAMC1, LAMA2 and LAMA3 gene polymorphisms and the risk for severe pelvic organ prolapse.LAMC1、LAMA2和LAMA3基因多态性与严重盆腔器官脱垂风险
Sci Bull (Beijing). 2019 Apr 15;64(7):466-468. doi: 10.1016/j.scib.2019.02.007. Epub 2019 Feb 14.
2
Distinctive structure, composition and biomechanics of collagen fibrils in vaginal wall connective tissues associated with pelvic organ prolapse.与盆腔器官脱垂相关的阴道壁结缔组织中胶原纤维的独特结构、组成和生物力学。
Acta Biomater. 2022 Oct 15;152:335-344. doi: 10.1016/j.actbio.2022.08.059. Epub 2022 Aug 31.
3
Pregnancy outcomes and associated factors for uterine rupture: an 8 years population-based retrospective study.
妊娠结局及子宫破裂相关因素的 8 年人群回顾性研究。
BMC Pregnancy Childbirth. 2022 Feb 1;22(1):91. doi: 10.1186/s12884-022-04415-6.
4
Esomeprazole inhibits hypoxia/endothelial dysfunction-induced autophagy in preeclampsia.埃索美拉唑抑制子痫前期缺氧/内皮功能障碍诱导的自噬。
Cell Tissue Res. 2022 Apr;388(1):181-194. doi: 10.1007/s00441-022-03587-z. Epub 2022 Jan 29.
5
Role of Fibroblasts and Myofibroblasts on the Pathogenesis and Treatment of Pelvic Organ Prolapse.成纤维细胞和肌成纤维细胞在盆腔器官脱垂发病机制和治疗中的作用。
Biomolecules. 2022 Jan 6;12(1):94. doi: 10.3390/biom12010094.
6
Advances in molecular mechanisms of pelvic organ prolapse (Review).盆腔器官脱垂分子机制的研究进展(综述)
Exp Ther Med. 2021 Sep;22(3):1009. doi: 10.3892/etm.2021.10442. Epub 2021 Jul 15.
7
The influence of hypertensive disorders during pregnancy on the perinatal outcome of different chorionic twins.妊娠期高血压疾病对不同绒毛膜性双胎围产结局的影响。
J Matern Fetal Neonatal Med. 2022 Dec;35(25):7146-7152. doi: 10.1080/14767058.2021.1945574. Epub 2021 Jun 27.
8
Commentary: systematic review and meta-analysis of genetic association studies of pelvic organ prolapse.述评:盆腔器官脱垂基因关联研究的系统评价与荟萃分析
Int Urogynecol J. 2022 Jan;33(1):83. doi: 10.1007/s00192-021-04834-7. Epub 2021 May 14.
9
Molecular mechanism of extracellular matrix disorder in pelvic organ prolapses.盆腔器官脱垂中外源性细胞基质紊乱的分子机制。
Mol Med Rep. 2020 Dec;22(6):4611-4618. doi: 10.3892/mmr.2020.11564. Epub 2020 Oct 6.
10
Genetic polymorphisms in collagen-related genes are associated with pelvic organ prolapse.胶原相关基因的遗传多态性与盆腔器官脱垂有关。
Menopause. 2020 Feb;27(2):223-229. doi: 10.1097/GME.0000000000001448.