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The Impact of BCL11A Polymorphisms on Endometrial Cancer Risk Among Chinese Han Females
BACKGROUND: Endometrial carcinoma (EC) is one of the most common malignant gynecological malignancies. BCL11A gene may have a tumor-suppressor role in EC. Until now, no studies have reported the effect of BCL11A variants on EC predisposition in Chinese population. METHODS: Six BCL11A polymorphisms w...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9000540/ https://www.ncbi.nlm.nih.gov/pubmed/35418772 http://dx.doi.org/10.2147/PGPM.S345772 |
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author | Cai, Junhong Peng, Siyuan Wang, Haibo Bao, Shan |
author_facet | Cai, Junhong Peng, Siyuan Wang, Haibo Bao, Shan |
author_sort | Cai, Junhong |
collection | PubMed |
description | BACKGROUND: Endometrial carcinoma (EC) is one of the most common malignant gynecological malignancies. BCL11A gene may have a tumor-suppressor role in EC. Until now, no studies have reported the effect of BCL11A variants on EC predisposition in Chinese population. METHODS: Six BCL11A polymorphisms were genotyped using Agena MassARRAY system among 509 EC patients and 506 matched healthy women. Risk assessment of the BCL11A polymorphisms for EC risk was performed by calculating odds ratios (OR) with 95% confidence intervals (CI) through logistic regression models. RESULTS: We found that rs7581162 (OR = 1.29, p = 0.012), rs10189857 (OR = 1.26, p = 0.028), rs1427407 (OR = 1.30, p = 0.015), rs766432 (OR = 1.27, p = 0.025), and rs6729815 (OR = 1.32, p = 0.008) in BCL11A were associated with higher susceptibility to EC in Chinese Han women. Age and BMI stratified analysis displayed that the risk association between BCL11A variants and EC predisposition might be age- and BMI-dependent. Haplotype analysis revealed that A(rs10189857)T(rs1427407) and G(rs10189857)G(rs1427407) haplotypes were related to an increased risk of EC. MDR analysis indicated that rs1427407 was the most influential attributor on EC risk in the single-locus model, and the best combination was the two-locus model containing rs7581162 and rs766432. CONCLUSION: Our study provided the first evidence that rs7581162, rs10189857, rs1427407, rs766432, and rs6729815 in BCL11A were risk factors for EC in Chinese Han women. These findings add our understanding of the role of BCL11A gene in EC pathogenesis. |
format | Online Article Text |
id | pubmed-9000540 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-90005402022-04-12 The Impact of BCL11A Polymorphisms on Endometrial Cancer Risk Among Chinese Han Females Cai, Junhong Peng, Siyuan Wang, Haibo Bao, Shan Pharmgenomics Pers Med Original Research BACKGROUND: Endometrial carcinoma (EC) is one of the most common malignant gynecological malignancies. BCL11A gene may have a tumor-suppressor role in EC. Until now, no studies have reported the effect of BCL11A variants on EC predisposition in Chinese population. METHODS: Six BCL11A polymorphisms were genotyped using Agena MassARRAY system among 509 EC patients and 506 matched healthy women. Risk assessment of the BCL11A polymorphisms for EC risk was performed by calculating odds ratios (OR) with 95% confidence intervals (CI) through logistic regression models. RESULTS: We found that rs7581162 (OR = 1.29, p = 0.012), rs10189857 (OR = 1.26, p = 0.028), rs1427407 (OR = 1.30, p = 0.015), rs766432 (OR = 1.27, p = 0.025), and rs6729815 (OR = 1.32, p = 0.008) in BCL11A were associated with higher susceptibility to EC in Chinese Han women. Age and BMI stratified analysis displayed that the risk association between BCL11A variants and EC predisposition might be age- and BMI-dependent. Haplotype analysis revealed that A(rs10189857)T(rs1427407) and G(rs10189857)G(rs1427407) haplotypes were related to an increased risk of EC. MDR analysis indicated that rs1427407 was the most influential attributor on EC risk in the single-locus model, and the best combination was the two-locus model containing rs7581162 and rs766432. CONCLUSION: Our study provided the first evidence that rs7581162, rs10189857, rs1427407, rs766432, and rs6729815 in BCL11A were risk factors for EC in Chinese Han women. These findings add our understanding of the role of BCL11A gene in EC pathogenesis. Dove 2022-04-07 /pmc/articles/PMC9000540/ /pubmed/35418772 http://dx.doi.org/10.2147/PGPM.S345772 Text en © 2022 Cai et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Cai, Junhong Peng, Siyuan Wang, Haibo Bao, Shan The Impact of BCL11A Polymorphisms on Endometrial Cancer Risk Among Chinese Han Females |
title | The Impact of BCL11A Polymorphisms on Endometrial Cancer Risk Among Chinese Han Females |
title_full | The Impact of BCL11A Polymorphisms on Endometrial Cancer Risk Among Chinese Han Females |
title_fullStr | The Impact of BCL11A Polymorphisms on Endometrial Cancer Risk Among Chinese Han Females |
title_full_unstemmed | The Impact of BCL11A Polymorphisms on Endometrial Cancer Risk Among Chinese Han Females |
title_short | The Impact of BCL11A Polymorphisms on Endometrial Cancer Risk Among Chinese Han Females |
title_sort | impact of bcl11a polymorphisms on endometrial cancer risk among chinese han females |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9000540/ https://www.ncbi.nlm.nih.gov/pubmed/35418772 http://dx.doi.org/10.2147/PGPM.S345772 |
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