The DNA methylation status of genes encoding Matrix metalloproteinases and tissue inhibitors of Matrix metalloproteinases in endometriosis

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AI-generated summary by claude@2026-06, 2026-06-07

This study found that DNA methylation in the promoter regions of MMP2, MMP3, MMP7, TIMP3, and TIMP4 genes was altered in endometriosis lesions, with MMP2 showing a negative correlation between methylation and transcript abundance.

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Abstract

Endometriosis is a benign disease, with malignant properties. A necessary step in the progression of endometriosis is tissue remodeling, which is coordinated by the activities of matrix metalloproteinases (MMPs) and tissue inhibitors of matrix metalloproteinases (TIMPs). This study evaluated the regulation of abnormal MMP and TIMP gene expression during endometriosis. Among the two genes families, promoter regions of MMP2, MMP3, MMP7, TIMP3, and TIMP4 were significantly altered in proliferative-phase endometriotic lesions compared to menstrual cycle-matched eutopic tissue from endometriosis-free women. In addition, a negative correlation was found between the DNA methylation status of the promoter region and transcript abundance of MMP2. Our findings suggest that changes in DNA methylation at the promoter region of MMP2 could underlie the changes in its expression in the ectopic endometria from patients with endometriosis.

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Condition tags

mesh:D004715endometriosis

MeSH descriptors

DNA Methylation Endometriosis Matrix Metalloproteinase 2 Promoter Regions, Genetic DNA Methylation Endometriosis Endometriosis Female Gene Expression Regulation Gene Expression Regulation Humans Matrix Metalloproteinase 2 Matrix Metalloproteinase 3 Matrix Metalloproteinase 3 Matrix Metalloproteinase 7 Matrix Metalloproteinase 7 Menstrual Cycle Menstrual Cycle Promoter Regions, Genetic Tissue Inhibitor of Metalloproteinase-3

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References (38)

Cited by (10)

Source provenance

europepmc
last seen: 2026-06-04T01:30:01.192114+00:00
openalex
last seen: 2026-06-04T00:00:01.174412+00:00
pubmed
last seen: 2026-05-13T22:20:07.505861+00:00
License: CC0 · commercial use OK