Association study between the polymorphisms of angiogenesis‐related genes and cervical cancer susceptibility in Chinese Uygur population

Abstract Background Cervical cancer is the second most common malignant tumor in women, and its invasion and metastasis are regulated by tumor angiogenic growth factors and their cognate receptors. In this study, we explored the relationship between genetic polymorphisms of angiogenesis‐related gene...

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Main Authors: Lili Han, Sulaiya Husaiyin, Chunhua Ma, Mayinuer Niyazi
Format: Article
Language:English
Published: Wiley 2019-10-01
Series:Molecular Genetics & Genomic Medicine
Subjects:
Online Access:https://doi.org/10.1002/mgg3.899
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author Lili Han
Sulaiya Husaiyin
Chunhua Ma
Mayinuer Niyazi
author_facet Lili Han
Sulaiya Husaiyin
Chunhua Ma
Mayinuer Niyazi
author_sort Lili Han
collection DOAJ
description Abstract Background Cervical cancer is the second most common malignant tumor in women, and its invasion and metastasis are regulated by tumor angiogenic growth factors and their cognate receptors. In this study, we explored the relationship between genetic polymorphisms of angiogenesis‐related genes (VEGF‐C, VEGFR‐2, and VEGFR‐3) and the risk of cervical cancer in Chinese Uygur population. Methods We investigated four single‐nucleotide polymorphisms (SNPs) in 342 cervical cancer cases and 498 controls to evaluate their association with the risk of cervical cancer. Their correlations were evaluated by chi‐squared test, Fisher's exact test, t test, and genetic model analyses. Odds ratios (ORs) and 95% confidence intervals (95% CIs) were calculated using unconditional logistic regression. Results We observed that rs12646659 in VEGF‐C was associated with a lower cervical cancer risk in allele, dominant, and log‐additive models (allele: p = .017; dominant: p = .018; log‐additive: p = .018). For the individuals older than 43, rs4604006 (VEGF‐C) was related to an increased cervical cancer risk under codominant model (p = .035), and rs12646659 was significantly associated with a reduced cervical cancer risk in allele, dominant, log‐additive models (allele: p = .028; codominant: p = .037; log‐additive: p = .037) However, there were no significant correlation of rs1000611 (VEGFR‐2) and rs1195571 (VEGFR‐3) with cervical cancer risk in Chinese Uygur population. Conclusion Our study firstly provided evidence that rs4604006 and rs12646659 of VEGF‐C gene were related to the susceptibility of cervical cancer in Chinese Uygur population.
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spelling doaj.art-5355404b87ca4f009e6bb46350b654102024-02-21T10:29:27ZengWileyMolecular Genetics & Genomic Medicine2324-92692019-10-01710n/an/a10.1002/mgg3.899Association study between the polymorphisms of angiogenesis‐related genes and cervical cancer susceptibility in Chinese Uygur populationLili Han0Sulaiya Husaiyin1Chunhua Ma2Mayinuer Niyazi3Department of Gynecology People’s Hospital of Xinjiang Uygur Autonomous Region Urumqi ChinaDepartment of Gynecology People’s Hospital of Xinjiang Uygur Autonomous Region Urumqi ChinaDepartment of Gynecology People’s Hospital of Xinjiang Uygur Autonomous Region Urumqi ChinaDepartment of Gynecology People’s Hospital of Xinjiang Uygur Autonomous Region Urumqi ChinaAbstract Background Cervical cancer is the second most common malignant tumor in women, and its invasion and metastasis are regulated by tumor angiogenic growth factors and their cognate receptors. In this study, we explored the relationship between genetic polymorphisms of angiogenesis‐related genes (VEGF‐C, VEGFR‐2, and VEGFR‐3) and the risk of cervical cancer in Chinese Uygur population. Methods We investigated four single‐nucleotide polymorphisms (SNPs) in 342 cervical cancer cases and 498 controls to evaluate their association with the risk of cervical cancer. Their correlations were evaluated by chi‐squared test, Fisher's exact test, t test, and genetic model analyses. Odds ratios (ORs) and 95% confidence intervals (95% CIs) were calculated using unconditional logistic regression. Results We observed that rs12646659 in VEGF‐C was associated with a lower cervical cancer risk in allele, dominant, and log‐additive models (allele: p = .017; dominant: p = .018; log‐additive: p = .018). For the individuals older than 43, rs4604006 (VEGF‐C) was related to an increased cervical cancer risk under codominant model (p = .035), and rs12646659 was significantly associated with a reduced cervical cancer risk in allele, dominant, log‐additive models (allele: p = .028; codominant: p = .037; log‐additive: p = .037) However, there were no significant correlation of rs1000611 (VEGFR‐2) and rs1195571 (VEGFR‐3) with cervical cancer risk in Chinese Uygur population. Conclusion Our study firstly provided evidence that rs4604006 and rs12646659 of VEGF‐C gene were related to the susceptibility of cervical cancer in Chinese Uygur population.https://doi.org/10.1002/mgg3.899cervical cancergenetics polymorphismsVEGF‐CVEGFR‐2VEGFR‐3
spellingShingle Lili Han
Sulaiya Husaiyin
Chunhua Ma
Mayinuer Niyazi
Association study between the polymorphisms of angiogenesis‐related genes and cervical cancer susceptibility in Chinese Uygur population
Molecular Genetics & Genomic Medicine
cervical cancer
genetics polymorphisms
VEGF‐C
VEGFR‐2
VEGFR‐3
title Association study between the polymorphisms of angiogenesis‐related genes and cervical cancer susceptibility in Chinese Uygur population
title_full Association study between the polymorphisms of angiogenesis‐related genes and cervical cancer susceptibility in Chinese Uygur population
title_fullStr Association study between the polymorphisms of angiogenesis‐related genes and cervical cancer susceptibility in Chinese Uygur population
title_full_unstemmed Association study between the polymorphisms of angiogenesis‐related genes and cervical cancer susceptibility in Chinese Uygur population
title_short Association study between the polymorphisms of angiogenesis‐related genes and cervical cancer susceptibility in Chinese Uygur population
title_sort association study between the polymorphisms of angiogenesis related genes and cervical cancer susceptibility in chinese uygur population
topic cervical cancer
genetics polymorphisms
VEGF‐C
VEGFR‐2
VEGFR‐3
url https://doi.org/10.1002/mgg3.899
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