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Expression and Epigenetic Change of the AR and FSHR Genes in the Granulosa Cells of Endometriosis Patients.

Authors :
Mika Hayashi
Yoshiki Yamashita
Atsushi Hayashi
Yoko Yoshida
Sachiko Kawabe
Masami Hayashi
Yoshito Terai
Hideki Kamegai
Masahide Ohmichi
Source :
Genetics & Epigenetics. 2012, Issue 4, p1-8. 8p.
Publication Year :
2012

Abstract

Background: Endometriosis is one of the most common gynecological diseases associated with infertility. Endometriosis may affect the androgen receptor (AR) mRNA expression in human granulosa cells and the methylation of the promoter region of AR. We investigated 28 patients with endometriosis and 47 subjects without endometriosis undertaking IVF treatment. Methods: Granulosa cells were obtained from 28 patients with endometriosis and 47 subjects without endometriosis as a control. Expressions of AR and FSHR mRNA were then evaluated by OneStep real-time PCR analysis, and the level of methylation of the promoter region was qualified by methylation-specified PCR (MSP). Results: The expression of AR mRNA in the endometriosis group was statistically lower than that in the control group. As well, FSHR mRNA expression in the control group showed a positive correlation with AR mRNA expression; however, there was no such correlation in endometriosis patients. In the control group, AR mRNA expression was statistically higher in pregnant subjects compared with non-pregnant subjects; however, in the endometriosis group, no significant difference was identified. The promoter of AR was heavily methylated in all endometriosis cases; however, only 5 (45.4%) were methylated in the control group. Conclusion: Lower AR mRNA expression and methylation of the AR promoter region might affect the expression of AR and FSHR in the presence of endometriosis, thus leading to a disturbance in the regulation of AR and FSHR. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
1179237X
Issue :
4
Database :
Academic Search Index
Journal :
Genetics & Epigenetics
Publication Type :
Academic Journal
Accession number :
89392923
Full Text :
https://doi.org/10.4137/GEG.S9877