Interaction between XRCC2 gene polymorphism and abdominal obesity on risk of endometrial carcinoma

Aims The aim of this study was to investigate the impact of three single nucleotide polymorphisms (SNPs) within X-Ray Repair Cross Complementary Group 2 (XRCC2) gene and additional gene- abdominal obesity (AO) interaction with endometrial carcinoma (EC) risk.Methods Hardy–Weinberg equilibrium was te...

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Main Authors: Wenjuan Tian, Siyu Cao, Wei Zhang, Chenlian Quan, Meiqin Zhang, Yan Huang
Format: Article
Language:English
Published: Taylor & Francis Group 2024-12-01
Series:Gynecological Endocrinology
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Online Access:https://www.tandfonline.com/doi/10.1080/09513590.2024.2317270
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author Wenjuan Tian
Siyu Cao
Wei Zhang
Chenlian Quan
Meiqin Zhang
Yan Huang
author_facet Wenjuan Tian
Siyu Cao
Wei Zhang
Chenlian Quan
Meiqin Zhang
Yan Huang
author_sort Wenjuan Tian
collection DOAJ
description Aims The aim of this study was to investigate the impact of three single nucleotide polymorphisms (SNPs) within X-Ray Repair Cross Complementary Group 2 (XRCC2) gene and additional gene- abdominal obesity (AO) interaction with endometrial carcinoma (EC) risk.Methods Hardy–Weinberg equilibrium was tested for all participants by using SNPstats (online software: http://bioinfo.iconcologia.net/SNPstats). The best SNP–SNP and gene–AO interaction combination among three SNPs within XRCC2 gene and AO was screened using generalized multifactor dimensionality reduction (GMDR).Results We employed the logistic regression analysis showed that rs718282-T allele is associated with increased EC risk, adjusted ORs (95%CI) were 1.67 (1.23–2.04). However, we did not find statistical association between rs3218536, and rs3218384 and EC susceptibility. GMDR analysis was used for SNP-SNP- and gene-abdominal obesity analysis. The cross-validation consistency and the testing accuracy for the interaction were calculated. The two-locus model between rs718282 and AO had a testing accuracy of 60.11%, which was significant at the p < .001 level, and this two- locus model was considered as the best model. It provided statistical evidence for rs718282 gene–AO interaction effects. The results indicated that AO influenced the EC risk depending on the rs718282 genotypes. Compared with non- AO subjects with rs718282–CC genotype, AO subjects with rs718282-CT or TT genotype had the highest EC risk, OR (95%CI) was 2.83 (1.67 − 4.02), after covariates adjustment.Conclusions Both the rs718282- T allele, and its interaction with AO were associated with increased EC risk.
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spelling doaj-art-e155cb4a67e147bfaa2a615cd71f863d2025-08-20T02:39:22ZengTaylor & Francis GroupGynecological Endocrinology0951-35901473-07662024-12-0140110.1080/09513590.2024.2317270Interaction between XRCC2 gene polymorphism and abdominal obesity on risk of endometrial carcinomaWenjuan Tian0Siyu Cao1Wei Zhang2Chenlian Quan3Meiqin Zhang4Yan Huang5Department of Oncology, Shanghai Medical College of Fudan University, Shanghai, ChinaDepartment of Oncology, Shanghai Medical College of Fudan University, Shanghai, ChinaDepartment of Oncology, Shanghai Medical College of Fudan University, Shanghai, ChinaDepartment of Oncology, Shanghai Medical College of Fudan University, Shanghai, ChinaDepartment of Oncology, Shanghai Medical College of Fudan University, Shanghai, ChinaDepartment of Oncology, Shanghai Medical College of Fudan University, Shanghai, ChinaAims The aim of this study was to investigate the impact of three single nucleotide polymorphisms (SNPs) within X-Ray Repair Cross Complementary Group 2 (XRCC2) gene and additional gene- abdominal obesity (AO) interaction with endometrial carcinoma (EC) risk.Methods Hardy–Weinberg equilibrium was tested for all participants by using SNPstats (online software: http://bioinfo.iconcologia.net/SNPstats). The best SNP–SNP and gene–AO interaction combination among three SNPs within XRCC2 gene and AO was screened using generalized multifactor dimensionality reduction (GMDR).Results We employed the logistic regression analysis showed that rs718282-T allele is associated with increased EC risk, adjusted ORs (95%CI) were 1.67 (1.23–2.04). However, we did not find statistical association between rs3218536, and rs3218384 and EC susceptibility. GMDR analysis was used for SNP-SNP- and gene-abdominal obesity analysis. The cross-validation consistency and the testing accuracy for the interaction were calculated. The two-locus model between rs718282 and AO had a testing accuracy of 60.11%, which was significant at the p < .001 level, and this two- locus model was considered as the best model. It provided statistical evidence for rs718282 gene–AO interaction effects. The results indicated that AO influenced the EC risk depending on the rs718282 genotypes. Compared with non- AO subjects with rs718282–CC genotype, AO subjects with rs718282-CT or TT genotype had the highest EC risk, OR (95%CI) was 2.83 (1.67 − 4.02), after covariates adjustment.Conclusions Both the rs718282- T allele, and its interaction with AO were associated with increased EC risk.https://www.tandfonline.com/doi/10.1080/09513590.2024.2317270Abdominal obesityendometrial carcinomainteractionsingle nucleotide polymorphismsX-ray repair cross-complementing group
spellingShingle Wenjuan Tian
Siyu Cao
Wei Zhang
Chenlian Quan
Meiqin Zhang
Yan Huang
Interaction between XRCC2 gene polymorphism and abdominal obesity on risk of endometrial carcinoma
Gynecological Endocrinology
Abdominal obesity
endometrial carcinoma
interaction
single nucleotide polymorphisms
X-ray repair cross-complementing group
title Interaction between XRCC2 gene polymorphism and abdominal obesity on risk of endometrial carcinoma
title_full Interaction between XRCC2 gene polymorphism and abdominal obesity on risk of endometrial carcinoma
title_fullStr Interaction between XRCC2 gene polymorphism and abdominal obesity on risk of endometrial carcinoma
title_full_unstemmed Interaction between XRCC2 gene polymorphism and abdominal obesity on risk of endometrial carcinoma
title_short Interaction between XRCC2 gene polymorphism and abdominal obesity on risk of endometrial carcinoma
title_sort interaction between xrcc2 gene polymorphism and abdominal obesity on risk of endometrial carcinoma
topic Abdominal obesity
endometrial carcinoma
interaction
single nucleotide polymorphisms
X-ray repair cross-complementing group
url https://www.tandfonline.com/doi/10.1080/09513590.2024.2317270
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