Polymorphic variants of DNMT3A and the risk of endometriosis

被引:8
|
作者
Szczepanska, Malgorzata
Mostowska, Adrianna [1 ]
Wirstlein, Przemyslaw [1 ]
Malejczyk, Jacek [2 ]
Ploski, Rafal [3 ]
Skrzypczak, Jana
Jagodzinski, Pawel P. [1 ]
机构
[1] Poznan Univ Med Sci, Dept Biochem & Mol Biol, PL-60781 Poznan, Poland
[2] Dept Histol & Embryol, Lublin, Poland
[3] Med Univ Warsaw, Dept Med Genet, Ctr Biostruct Res, Warsaw, Poland
关键词
Polymorphisms; Endometriosis; Infertility; DNMT3A; SINGLE-NUCLEOTIDE POLYMORPHISMS; DNA METHYLTRANSFERASES; ABERRANT EXPRESSION; POSSIBLE MECHANISM; GENE-EXPRESSION; DOWN-REGULATION; STROMAL CELLS; INFERTILITY; WOMEN; METHYLATION;
D O I
10.1016/j.ejogrb.2012.09.003
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: Overexpression of DNA methyltransferase 3A (DNMT3A) and aberrant methylation of various genes in eutopic endometrium have been demonstrated in women with endometriosis. We aimed to study whether DNMT3A polymorphisms could be a genetic risk factor for endometriosis and endometriosis-related infertility. Study design: We studied 5 SNPs (rs2289195, rs7590760, rs13401241, rs749131 and rs1550117) located in the DNMT3A gene in 357 women with endometriosis and 640 controls. Results: We did not observe significant differences between genotype and allele frequencies of rs2289195, rs7590760, rs13401241, rs749131 and rs1550117 SNPs in women with endometriosis, endometriosis-related infertility, and controls. The lowest p values of the trend test were observed for DNMT3A rs1550117 in endometriosis and endometriosis-related infertility (p(trend) = 0.049 and p(trend) = 0.055, respectively). Conclusions: Our results did not supply evidence for the contribution of SNPs located in DNMT3A to either endometriosis or endometriosis-related infertility. (C) 2012 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:81 / 85
页数:5
相关论文
共 50 条
  • [21] DNMT1, DNMT3A and DNMT3B Polymorphisms Associated With Gastric Cancer Risk: A Systematic Review and Meta-analysis
    Li, Hongjia
    Li, Wen
    Liu, Shanshan
    Zong, Shaoqi
    Wang, Weibing
    Ren, Jianlin
    Li, Qi
    Hou, Fenggang
    Shi, Qi
    EBIOMEDICINE, 2016, 13 : 125 - 131
  • [22] DNMT3A mutations in acute myeloid leukemia
    Shah, Mrinal Y.
    Licht, Jonathan D.
    NATURE GENETICS, 2011, 43 (04) : 289 - 290
  • [23] Selective role for DNMT3a in learning and memory
    Morris, Michael J.
    Adachi, Megumi
    Na, Elsa S.
    Monteggia, Lisa M.
    NEUROBIOLOGY OF LEARNING AND MEMORY, 2014, 115 : 30 - 37
  • [24] WTAP gene variants and susceptibility to ovarian endometriosis in a Chinese population
    Wan, Zixian
    Ye, Lu
    Chen, Guange
    Xiong, Chaoyi
    Ouyang, Zhenbo
    Wu, Liangzhi
    He, Jing
    Duan, Ping
    Jie, Youkun
    Zhang, Qiushi
    Hua, Wenfeng
    FRONTIERS IN GENETICS, 2023, 14
  • [25] DNA Demethylation by DNMT3A and DNMT3B in vitro and of Methylated Episomal DNA in Transiently Transfected Cells
    Chatterjee, Biswanath
    Lin, Miao-Hsia
    Chen, Chun-Chang
    Peng, Kai-Lin
    Wu, Mu-Sheng
    Tseng, Mei-Chun
    Chen, Yu-Ju
    Shen, Che-Kun James
    BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS, 2018, 1861 (11): : 1048 - 1061
  • [26] Polymorphic variants in the dopamine receptor D2 in women with endometriosis-related infertility
    Szczepanska, Malgorzata
    Mostowska, Adrianna
    Wirstlein, Przemyslaw
    Skrzypczak, Jana
    Misztal, Matthew
    Jagodzinski, Pawel P.
    MOLECULAR MEDICINE REPORTS, 2015, 12 (02) : 3055 - 3060
  • [27] DNMT1 and DNMT3A Gene Polymorphisms and Early Pregnancy Loss
    Ahmed, A. A. M.
    Azova, M. M.
    Ramazanova, F. U.
    Gigani, B.
    RUSSIAN JOURNAL OF GENETICS, 2020, 56 (03) : 379 - 382
  • [28] Evaluation of DNMT3A genetic polymorphisms as outcome predictors in AML patients
    Yuan, Xiao-Qing
    Zhang, Dao-Yu
    Yan, Han
    Yang, Yong-Long
    Zhu, Ke-Wei
    Chen, Yan-Hong
    Li, Xi
    Yin, Ji-Ye
    Li, Xiao-Lin
    Zeng, Hui
    Chen, Xiao-Ping
    ONCOTARGET, 2016, 7 (37) : 60555 - 60574
  • [29] DNMT3A and DNMT3B Targeting as an Effective Radiosensitizing Strategy in Embryonal Rhabdomyosarcoma
    Camero, Simona
    Vitali, Giulia
    Pontecorvi, Paola
    Ceccarelli, Simona
    Anastasiadou, Eleni
    Cicchetti, Francesca
    Flex, Elisabetta
    Pomella, Silvia
    Cassandri, Matteo
    Rota, Rossella
    Marampon, Francesco
    Marchese, Cinzia
    Schiavetti, Amalia
    Megiorni, Francesca
    CELLS, 2021, 10 (11)
  • [30] DNMT3A Mutations in Acute Myeloid Leukemia.
    Ley, Timothy J.
    Ding, Li
    Walter, Matthew J.
    McLellan, Michael D.
    Lamprecht, Tamara
    Larson, David E.
    Kandoth, Cyriac
    Payton, Jacqueline E.
    Baty, Jack
    Welch, John
    Harris, Christopher C.
    Lichti, Cheryl F.
    Townsend, R. Reid
    Fulton, Robert S.
    Dooling, David J.
    Koboldt, Daniel C.
    Schmidt, Heather
    Zhang, Qunyuan
    Osborne, John R.
    Lin, Ling
    O'Laughlin, Michelle
    McMichael, Joshua F.
    Delehaunty, Kim D.
    McGrath, Sean D.
    Fulton, Lucinda A.
    Magrini, Vincent J.
    Vickery, Tammi L.
    Hundal, Jasreet
    Cook, Lisa L.
    Conyers, Joshua J.
    Swift, Gary W.
    Reed, Jerry P.
    Alldredge, Patricia A.
    Wylie, Todd
    Walker, Jason
    Kalicki, Joelle
    Watson, Mark A.
    Heath, Sharon
    Shannon, William D.
    Varghese, Nobish
    Nagarajan, Rakesh
    Westervelt, Peter
    Tomasson, Michael H.
    Link, Daniel C.
    Graubert, Timothy A.
    DiPersio, John F.
    Mardis, Elaine R.
    Wilson, Richard K.
    NEW ENGLAND JOURNAL OF MEDICINE, 2010, 363 (25) : 2424 - 2433