The association between MTHFR polymorphism and cervical cancer

Abstract Cervical cancer is an extremely prevalent disease worldwide. The purpose of this study was to illustrate the relationship between methylenetetrahydrofolate reductase (MTHFR) polymorphisms or methionine synthase reductase (MTRR) polymorphisms and cervical cancer. There were 372 women who per...

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Main Authors: Jiao-Mei Gong, Yong Shen, Wan-Wan Shan, Yan-Xia He
Format: Article
Language:English
Published: Nature Publishing Group 2018-05-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-018-25726-9
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spelling doaj-7a93e23ab26b4717808731edb6ba5d6d2020-12-08T04:00:27ZengNature Publishing GroupScientific Reports2045-23222018-05-01811710.1038/s41598-018-25726-9The association between MTHFR polymorphism and cervical cancerJiao-Mei Gong0Yong Shen1Wan-Wan Shan2Yan-Xia He3Department of Clinical Laboratory, Second Affiliated Hospital of Zhengzhou UniversityDepartment of Clinical Laboratory, Affiliated Cancer Hospital of Zhengzhou University & Henan Cancer HospitalDepartment of Obstetrics and Gynecology, Third Affiliated Hospital of Zhengzhou UniversityDepartment of Clinical Laboratory, Second Affiliated Hospital of Zhengzhou UniversityAbstract Cervical cancer is an extremely prevalent disease worldwide. The purpose of this study was to illustrate the relationship between methylenetetrahydrofolate reductase (MTHFR) polymorphisms or methionine synthase reductase (MTRR) polymorphisms and cervical cancer. There were 372 women who performed genetic and folic acid assessments. For the MTHFR C677T, there was no significant difference in the distribution of C allele and T allele in the three groups. However, the mutant C allele of MTHFR A1298C was significantly higher in the cancer group than in the normal group. Similarly, the mutant G allele of MTRR A66G was also higher than the normal group. The serum folic acid levels were gradually decreased with the development of cervical lesions. Serum folate levels in 4–9 ng/ml and ≤4 ng/ml were both significantly associated with cervical cancer risk. However, the MTHFR C677T polymorphism was not associated with the risk of cervical cancer or CIN. In contrast, the MTHFR A1298C polymorphism could increase the risk of both cervical cancer and CIN. In addition, the MTRR A66G polymorphism was only associated with the risk of cervical cancer but not CIN.https://doi.org/10.1038/s41598-018-25726-9
collection DOAJ
language English
format Article
sources DOAJ
author Jiao-Mei Gong
Yong Shen
Wan-Wan Shan
Yan-Xia He
spellingShingle Jiao-Mei Gong
Yong Shen
Wan-Wan Shan
Yan-Xia He
The association between MTHFR polymorphism and cervical cancer
Scientific Reports
author_facet Jiao-Mei Gong
Yong Shen
Wan-Wan Shan
Yan-Xia He
author_sort Jiao-Mei Gong
title The association between MTHFR polymorphism and cervical cancer
title_short The association between MTHFR polymorphism and cervical cancer
title_full The association between MTHFR polymorphism and cervical cancer
title_fullStr The association between MTHFR polymorphism and cervical cancer
title_full_unstemmed The association between MTHFR polymorphism and cervical cancer
title_sort association between mthfr polymorphism and cervical cancer
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2018-05-01
description Abstract Cervical cancer is an extremely prevalent disease worldwide. The purpose of this study was to illustrate the relationship between methylenetetrahydrofolate reductase (MTHFR) polymorphisms or methionine synthase reductase (MTRR) polymorphisms and cervical cancer. There were 372 women who performed genetic and folic acid assessments. For the MTHFR C677T, there was no significant difference in the distribution of C allele and T allele in the three groups. However, the mutant C allele of MTHFR A1298C was significantly higher in the cancer group than in the normal group. Similarly, the mutant G allele of MTRR A66G was also higher than the normal group. The serum folic acid levels were gradually decreased with the development of cervical lesions. Serum folate levels in 4–9 ng/ml and ≤4 ng/ml were both significantly associated with cervical cancer risk. However, the MTHFR C677T polymorphism was not associated with the risk of cervical cancer or CIN. In contrast, the MTHFR A1298C polymorphism could increase the risk of both cervical cancer and CIN. In addition, the MTRR A66G polymorphism was only associated with the risk of cervical cancer but not CIN.
url https://doi.org/10.1038/s41598-018-25726-9
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