Valproic acid-induced histone acetylation suppresses CYP19 gene expression and inhibits the growth and survival of endometrial stromal cells

被引:20
|
作者
Chen, Yu [1 ]
Cai, Shengyun [1 ]
Wang, Jingwen [1 ]
Xu, Mingjuan [1 ]
机构
[1] Second Mil Med Univ, Dept Obstet & Gynaecol, Changhai Hosp, Shanghai 200433, Peoples R China
关键词
valproic acid; CYP19; endometriosis; endometrial stromal cells; histone acetylation; DEACETYLASE INHIBITORS; THERAPEUTIC TARGET; PATHOGENESIS; AROMATASE; ESTROGEN; EPIGENETICS; MECHANISMS; APOPTOSIS; DISEASE;
D O I
10.3892/ijmm.2015.2263
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Endometriosis is a common type of estrogen-dependent, gynecological and chronic inflammatory disease. Epigenetics refers to changes in gene expression that occur without altering the DNA sequence or DNA content. Histone modification dominates epigenetics, and histone acetylation is the most extensively studied type of histone modification. The CYP19 gene is the gene that encodes P450 aromatase, which regulates the synthesis of estrogen. Hence, we conducted this study to investigate whether histone acetylation has an effect on CYP19 expression and whether histone acetylation is related to endometrial stromal cells (ESCs). Reverse transcription-quantitative polymerase chain reaction (RT-qPCR), western blot analysis and chromatin immunoprecipitation assays were performed. The results revealed that valproic acid (VPA) significantly promoted histone acetylation in the ESCs, which inhibited histone acetylation in the promoter region of the CYP19 gene, thus suppressing its expression. We also noted that VPA inhibited cell viability and proliferation, and induced the apoptosis, of ESCs. The findings of our study on histone acetylation, endometriosis and the CYP19 gene provide insight which may aid in the research of histone acetylation and suggest that the CYP19 gene may be a novel therapeutic target and method for the treatment of endometriosis.
引用
收藏
页码:725 / 732
页数:8
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