The role of genetic factors in developing endometrioid lesions

Q3 Medicine
T. A. Ponomareva, O. Altukhova, I. Ponomarenko, M. Churnosov
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引用次数: 0

Abstract

Here, we analyze the data on genetic factors involved in developing endometriosis available in current publications. To date, the genome-wide associative studies (GWAS) have revealed more than 190 loci associated with endometriosis development, however, only few polymorphisms were associated with this disease identified in two GWAS (rs1537377 CDKN2B-AS1, rs71575922 SYNE1, rs11674184 GREB1, rs1903068 KDR, rs2235529 WNT4, rs7412010 CDC42), and only one rs12700667 TSEN15P3/MIR148A polymorphic locus in four studies. Several polymorphisms located in the region of two genes GREB1 (rs11674184, rs13394619, rs35417544) and WNT4 (rs2235529, rs12037376, rs7521902) are associated with endometriosis in several GWAS. The association of 5 polymorphic loci with endometriosis was confirmed in two or more replication studies: rs13394619 GREB1, rs7521902 MIR4418/WNT4, rs1250248 FN1 and rs6542095 CKAP2L/IL1A – in two studies, rs12700667 TSEN15P3/MIR148A – in four studies. At the same time, the relationship between the vast majority of GWAS-significant polymorphic loci (more than 95 %) and endometriosis has not been confirmed in other independent studies, necessitating a need to continue endometriosis-related genetic studies, including those aimed at confirming previously identified associations.
遗传因素在发生子宫内膜样病变中的作用
在这里,我们分析了当前出版物中有关发生子宫内膜异位症的遗传因素的数据。迄今为止,全基因组关联研究(GWAS)已经发现了190多个与子宫内膜异位症相关的位点,然而,只有少数多态性在两个GWAS (rs1537377 CDKN2B-AS1、rs71575922 SYNE1、rs11674184 GREB1、rs1903068 KDR、rs2235529 WNT4、rs7412010 CDC42)中被发现,在四个研究中只有一个rs12700667 TSEN15P3/MIR148A多态性位点被发现。位于两个基因GREB1 (rs11674184, rs13394619, rs35417544)和WNT4 (rs2235529, rs12037376, rs7521902)区域的几个多态性与几种GWAS的子宫内膜异位症有关。5个多态性位点与子宫内膜异位症的关联在两个或多个复制研究中得到证实:rs13394619 GREB1, rs7521902 MIR4418/WNT4, rs1250248 FN1和rs6542095 CKAP2L/IL1A -在两个研究中,rs12700667 TSEN15P3/MIR148A -在四个研究中。同时,绝大多数gwas显著多态性位点(超过95%)与子宫内膜异位症之间的关系尚未在其他独立研究中得到证实,因此需要继续进行子宫内膜异位症相关的遗传研究,包括那些旨在确认先前确定的关联的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.00
自引率
0.00%
发文量
68
审稿时长
12 weeks
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