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Updated: Jun 4, 2026

Methyl-binding DNA capture Sequencing for Patient Tissues
Published on: October 31, 2016
Deoxyribonucleic acid methyltransferases and methyl-CpG-binding domain proteins in human endometrium and
Kim J A F van Kaam1, Bert Delvoux, Andrea Romano
1GROW, School for Oncology and Developmental Biology, University of Maastricht, Maastricht, the Netherlands. kimvankaam@yahoo.com
Objective:
To determine [1] expression levels of both DNA methyltransferases (DNMTs) and methyl-CpG-binding domain proteins (MBDs) in human endometrium throughout the menstrual cycle and in eutopic and ectopic endometrium of patients with endometriosis and [2] hormone responsiveness of DNMT and MBD expression in explant cultures of proliferative phase endometrium.
Design:
In vitro study.
Setting:
Academic medical center.
Patient(S):
Premenopausal women with and without endometriosis.
Intervention(S):
Explant cultures of proliferative phase endometrium were treated with vehicle, 17β-E(2), or a combination of E(2) and P (E(2) + P) for 24 hours.
Main Outcome Measure(S):
Expression levels of DNMT1, DNMT2, and DNMT3B and MBD1, MBD2, and MeCP2 with use of real-time quantitative polymerase chain reaction.
Result(S):
Expression levels of DNMT1 and MBD2 were significantly higher in secretory-phase endometrium compared with proliferative endometrium and menstrual endometrium. In explant cultures, treatment with E(2) + P resulted in significant up-regulation of DNMT1 and MBD2. Expression levels of several DNMTs and MBDs were significantly lower in endometriotic lesions compared with eutopic endometrium of women with endometriosis and disease-free controls.
Conclusion(S):
These findings suggest a role for DNMTs and MBDs in the growth and differentiation of the human endometrium and support the notion that endometriosis may be an epigenetic disease.
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