Racial disparity in uterine leiomyoma: new insights of genetic and environmental burden in myometrial cells
Abstract Uterine leiomyoma (LM), also known as uterine fibroids, are common gynecological tumors and can reach a prevalence of 70% among women by the age of 50 years. Notably, the LM burden is much higher in Black women with earlier onset, a greater tumor number, size, and severity compared to White...
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Veröffentlicht in: | Molecular human reproduction 2024-02, Vol.30 (3) |
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creator | Khan, Nazeer H McNally, Ross Kim, J Julie Wei, Jian-Jun |
description | Abstract
Uterine leiomyoma (LM), also known as uterine fibroids, are common gynecological tumors and can reach a prevalence of 70% among women by the age of 50 years. Notably, the LM burden is much higher in Black women with earlier onset, a greater tumor number, size, and severity compared to White women. Published knowledge shows that there are genetic, environmental, and lifestyle-based risk factors associated with racial disparity for LM. Significant strides have been made on genomic, epigenomic, and transcriptomic data levels in Black and White women to elucidate the underlying pathomolecular reasons of racial disparity in LM development. However, racial disparity of LM remains a major area of concern in gynecological research. This review highlights risk factors of LM and their role in different races. Furthermore, we discuss the genetics and uterine myometrial microenvironment in LM development. Comparative findings revealed that a major racial difference in the disease is linked to myometrial oxidative burden and altered ROS pathways which is relevant to the oxidized guanine in genomic DNA and MED12 mutations that drive the LM genesis. Considering the burden and morbidity of LM, we anticipate that this review on genetic risk and myometrial microenvironment will strengthen understanding and propel the growth of research to address the racial disparity of LM burden. |
doi_str_mv | 10.1093/molehr/gaae004 |
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Uterine leiomyoma (LM), also known as uterine fibroids, are common gynecological tumors and can reach a prevalence of 70% among women by the age of 50 years. Notably, the LM burden is much higher in Black women with earlier onset, a greater tumor number, size, and severity compared to White women. Published knowledge shows that there are genetic, environmental, and lifestyle-based risk factors associated with racial disparity for LM. Significant strides have been made on genomic, epigenomic, and transcriptomic data levels in Black and White women to elucidate the underlying pathomolecular reasons of racial disparity in LM development. However, racial disparity of LM remains a major area of concern in gynecological research. This review highlights risk factors of LM and their role in different races. Furthermore, we discuss the genetics and uterine myometrial microenvironment in LM development. Comparative findings revealed that a major racial difference in the disease is linked to myometrial oxidative burden and altered ROS pathways which is relevant to the oxidized guanine in genomic DNA and MED12 mutations that drive the LM genesis. Considering the burden and morbidity of LM, we anticipate that this review on genetic risk and myometrial microenvironment will strengthen understanding and propel the growth of research to address the racial disparity of LM burden.</description><identifier>ISSN: 1460-2407</identifier><identifier>EISSN: 1460-2407</identifier><identifier>DOI: 10.1093/molehr/gaae004</identifier><identifier>PMID: 38290796</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><ispartof>Molecular human reproduction, 2024-02, Vol.30 (3)</ispartof><rights>The Author(s) 2024. Published by Oxford University Press on behalf of European Society of Human Reproduction and Embryology. All rights reserved. For permissions, please email: journals.permissions@oup.com 2024</rights><rights>The Author(s) 2024. Published by Oxford University Press on behalf of European Society of Human Reproduction and Embryology. All rights reserved. For permissions, please email: journals.permissions@oup.com.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c329t-b4b84d8a3605d5065ac13aafab2d167ff81a1c38b1cf10ef6b283c7198f59cb03</citedby><cites>FETCH-LOGICAL-c329t-b4b84d8a3605d5065ac13aafab2d167ff81a1c38b1cf10ef6b283c7198f59cb03</cites><orcidid>0000-0002-9244-8683 ; 0000-0001-9834-8213 ; 0000-0003-0281-2793</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,1584,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38290796$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Khan, Nazeer H</creatorcontrib><creatorcontrib>McNally, Ross</creatorcontrib><creatorcontrib>Kim, J Julie</creatorcontrib><creatorcontrib>Wei, Jian-Jun</creatorcontrib><title>Racial disparity in uterine leiomyoma: new insights of genetic and environmental burden in myometrial cells</title><title>Molecular human reproduction</title><addtitle>Mol Hum Reprod</addtitle><description>Abstract
Uterine leiomyoma (LM), also known as uterine fibroids, are common gynecological tumors and can reach a prevalence of 70% among women by the age of 50 years. Notably, the LM burden is much higher in Black women with earlier onset, a greater tumor number, size, and severity compared to White women. Published knowledge shows that there are genetic, environmental, and lifestyle-based risk factors associated with racial disparity for LM. Significant strides have been made on genomic, epigenomic, and transcriptomic data levels in Black and White women to elucidate the underlying pathomolecular reasons of racial disparity in LM development. However, racial disparity of LM remains a major area of concern in gynecological research. This review highlights risk factors of LM and their role in different races. Furthermore, we discuss the genetics and uterine myometrial microenvironment in LM development. Comparative findings revealed that a major racial difference in the disease is linked to myometrial oxidative burden and altered ROS pathways which is relevant to the oxidized guanine in genomic DNA and MED12 mutations that drive the LM genesis. Considering the burden and morbidity of LM, we anticipate that this review on genetic risk and myometrial microenvironment will strengthen understanding and propel the growth of research to address the racial disparity of LM burden.</description><issn>1460-2407</issn><issn>1460-2407</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqFkE1LxDAQhoMo7rp69Sg56qG7SdOP1JssfsGCIHouSTrZjbbJmrTK_ntbuoo3TzMwz_swvAidUzKnpGCLxtWw8Yu1EEBIcoCmNMlIFCckP_yzT9BJCG-E0DxO-TGaMB4XJC-yKXp_FsqIGlcmbIU37Q4bi7sWvLGAazCu2blGXGMLX_0lmPWmDdhpvAYLrVFY2AqD_TTe2QZs25tk5yuwg2aIQusHvYK6DqfoSIs6wNl-ztDr3e3L8iFaPd0_Lm9WkWJx0UYykTypuGAZSauUZKlQlAmhhYwrmuVacyqoYlxSpSkBncmYM5XTguu0UJKwGbocvVvvPjoIbdmYMHwgLLgulHERkzRnJEl7dD6iyrsQPOhy600j_K6kpBwKLseCy33BfeBi7-5kA9Uv_tNoD1yNgOu2_8m-AZ_MiYY</recordid><startdate>20240229</startdate><enddate>20240229</enddate><creator>Khan, Nazeer H</creator><creator>McNally, Ross</creator><creator>Kim, J Julie</creator><creator>Wei, Jian-Jun</creator><general>Oxford University Press</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-9244-8683</orcidid><orcidid>https://orcid.org/0000-0001-9834-8213</orcidid><orcidid>https://orcid.org/0000-0003-0281-2793</orcidid></search><sort><creationdate>20240229</creationdate><title>Racial disparity in uterine leiomyoma: new insights of genetic and environmental burden in myometrial cells</title><author>Khan, Nazeer H ; McNally, Ross ; Kim, J Julie ; Wei, Jian-Jun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c329t-b4b84d8a3605d5065ac13aafab2d167ff81a1c38b1cf10ef6b283c7198f59cb03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Khan, Nazeer H</creatorcontrib><creatorcontrib>McNally, Ross</creatorcontrib><creatorcontrib>Kim, J Julie</creatorcontrib><creatorcontrib>Wei, Jian-Jun</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular human reproduction</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Khan, Nazeer H</au><au>McNally, Ross</au><au>Kim, J Julie</au><au>Wei, Jian-Jun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Racial disparity in uterine leiomyoma: new insights of genetic and environmental burden in myometrial cells</atitle><jtitle>Molecular human reproduction</jtitle><addtitle>Mol Hum Reprod</addtitle><date>2024-02-29</date><risdate>2024</risdate><volume>30</volume><issue>3</issue><issn>1460-2407</issn><eissn>1460-2407</eissn><abstract>Abstract
Uterine leiomyoma (LM), also known as uterine fibroids, are common gynecological tumors and can reach a prevalence of 70% among women by the age of 50 years. Notably, the LM burden is much higher in Black women with earlier onset, a greater tumor number, size, and severity compared to White women. Published knowledge shows that there are genetic, environmental, and lifestyle-based risk factors associated with racial disparity for LM. Significant strides have been made on genomic, epigenomic, and transcriptomic data levels in Black and White women to elucidate the underlying pathomolecular reasons of racial disparity in LM development. However, racial disparity of LM remains a major area of concern in gynecological research. This review highlights risk factors of LM and their role in different races. Furthermore, we discuss the genetics and uterine myometrial microenvironment in LM development. Comparative findings revealed that a major racial difference in the disease is linked to myometrial oxidative burden and altered ROS pathways which is relevant to the oxidized guanine in genomic DNA and MED12 mutations that drive the LM genesis. Considering the burden and morbidity of LM, we anticipate that this review on genetic risk and myometrial microenvironment will strengthen understanding and propel the growth of research to address the racial disparity of LM burden.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>38290796</pmid><doi>10.1093/molehr/gaae004</doi><orcidid>https://orcid.org/0000-0002-9244-8683</orcidid><orcidid>https://orcid.org/0000-0001-9834-8213</orcidid><orcidid>https://orcid.org/0000-0003-0281-2793</orcidid></addata></record> |
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title | Racial disparity in uterine leiomyoma: new insights of genetic and environmental burden in myometrial cells |
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