Genome-wide DNA methylation analysis reveals a potential mechanism for the pathogenesis and development of uterine leiomyomas.
Genome-wide DNA methylation analysis reveals a potential mechanism for the pathogenesis and development of uterine leiomyomas.
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DOI:
10.1371/journal.pone.0066632
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发表时间:
2013
期刊:
影响因子:
3.7
通讯作者:
Sugino N
中科院分区:
文献类型:
--
作者:
Maekawa R;Sato S;Yamagata Y;Asada H;Tamura I;Lee L;Okada M;Tamura H;Takaki E;Nakai A;Sugino N
The pathogenesis of uterine leiomyomas, the most common benign tumor in women, remains unclear. Since acquired factors such as obesity, hypertension and early menarche place women at greater risk for uterine leiomyomas, uterine leiomyomas may be associated with epigenetic abnormalities that are caused by unfavorable environmental exposures. Profiles of genome-wide DNA methylation and mRNA expression were investigated in leiomyomas and in myometrium with and without leiomyomas. Profiles of DNA methylation and mRNA expression in the myometrium with and without leiomyomas were quite similar while those in leiomyomas were distinct. We identified 120 genes whose DNA methylation and mRNA expression patterns differed between leiomyomas and the adjacent myometrium. The biological relevance of the aberrantly methylated and expressed genes was cancer process, including IRS1 that is related to transformation, and collagen-related genes such as COL4A1, COL4A2 and COL6A3. We also detected 22 target genes of estrogen receptor (ER) alpha, including apoptosis-related genes, that have aberrant DNA methylation in the promoter, suggesting that the aberrant epigenetic regulation of ER alpha-target genes contributes to the aberrant response to estrogen. Aberrant DNA methylation and its related transcriptional aberration were associated with cancer processes, which may represent a critical initial mechanism that triggers transformation of a single tumor stem cell that will eventually develop into a monoclonal leiomyoma tumor. The aberrant epigenetic regulation of ER alpha-target genes also may contribute to the aberrant response to estrogen, which is involved in the development of uterine leiomyomas after menarche.
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DOI:
10.1158/1541-7786.mcr-11-0605
发表时间:
2012-04
期刊:
Molecular cancer research : MCR
影响因子:
--
作者:
Greathouse KL;Bredfeldt T;Everitt JI;Lin K;Berry T;Kannan K;Mittelstadt ML;Ho SM;Walker CL
通讯作者:
Walker CL
影响因子:
3.7
作者:
Esposito DL;Aru F;Lattanzio R;Morgano A;Abbondanza M;Malekzadeh R;Bishehsari F;Valanzano R;Russo A;Piantelli M;Moschetta A;Lotti LV;Mariani-Costantini R
通讯作者:
Mariani-Costantini R
影响因子:
8
作者:
del Rincón, SV;Guo, Q;Miller, WH
通讯作者:
Miller, WH
影响因子:
1.8
作者:
Feng G;Du P;Krett NL;Tessel M;Rosen S;Kibbe WA;Lin SM
通讯作者:
Lin SM
影响因子:
14.9
作者:
Huang DW;Sherman BT;Tan Q;Kir J;Liu D;Bryant D;Guo Y;Stephens R;Baseler MW;Lane HC;Lempicki RA
通讯作者:
Lempicki RA