Literature DB >> 17303386

Protective association of MTHFR polymorphism on cervical intraepithelial neoplasia is modified by riboflavin status.

Chandrika J Piyathilake1, Maria Azrad, Maurizio Macaluso, Gary L Johanning, Phillip E Cornwell, Edward E Partridge, Douglas C Heimburger.   

Abstract

OBJECTIVES: We previously reported that women polymorphic for the methylenetetrahydrofolate reductase (MTHFR) gene were less likely to have cervical intraepithelial neoplasia (CIN) 2 or 3 (odds ratio [OR] 0.40, 95% confidence interval [CI] 0.21-0.78, P = 0.007). In the present study, we tested whether this protective association is modified by circulating riboflavin status in the same study population.
METHODS: Riboflavin status was assessed by the erythrocyte glutathione reductase assay and expressed in terms of an erythrocyte glutathione reductase activity coefficient. The status of MTHFR polymorphism, riboflavin, and circulating concentrations of folate, vitamins B12, A, E, and C, and total carotene were ascertained in 170 White and 265 African-American women positive for the cervical presence of high-risk human papilloma virus. Presence/absence of CIN 2 or 3 was determined histologically, and associations with risk factors were examined using multiple logistic regression. Eighty women with CIN 2 or 3 lesions were compared with 355 women without cervical lesions. Based on the median erythrocyte glutathione reductase activity coefficient of 1.4, women were grouped into low (>1.4) and high (< or =1.4) riboflavin status.
RESULTS: Women with MTHFR polymorphism and low riboflavin status were significantly less likely to have CIN 2 or 3 than was the referent group of women without the polymorphism and high riboflavin status (OR 0.35, 95% CI 0.13-0.92, P = 0.034). MTHFR polymorphism was not associated with CIN 2 or 3 in women with high riboflavin status (OR 0.51, 95% CI 0.22-1.19, P = 0.119), nor were any of the associations influenced by folate levels.
CONCLUSION: A further inactivation of polymorphic MTHFR by low riboflavin status and a resulting shift in the folate metabolic pathway toward DNA synthesis may explain these observations. The practical implications of this complex gene-nutrient-disease interaction will require further investigation.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17303386      PMCID: PMC2025704          DOI: 10.1016/j.nut.2006.12.006

Source DB:  PubMed          Journal:  Nutrition        ISSN: 0899-9007            Impact factor:   4.008


  24 in total

1.  Association of the C677T polymorphism in the MTHFR gene with breast and/or ovarian cancer risk in Jewish women.

Authors:  R Gershoni-Baruch; E Dagan; D Israeli; L Kasinetz; E Kadouri; E Friedman
Journal:  Eur J Cancer       Date:  2000-12       Impact factor: 9.162

Review 2.  Chromosomal biomarkers of genomic instability relevant to cancer.

Authors:  Michael Fenech
Journal:  Drug Discov Today       Date:  2002-11-15       Impact factor: 7.851

3.  Methylenetetrahydrofolate reductase: a link between folate and riboflavin?

Authors:  Rima Rozen
Journal:  Am J Clin Nutr       Date:  2002-08       Impact factor: 7.045

4.  Association of methylenetetrahydrofolate reductase polymorphism C677T and dietary folate with the risk of cervical dysplasia.

Authors:  M T Goodman; K McDuffie; B Hernandez; L R Wilkens; C C Bertram; J Killeen; L Le Marchand; J Selhub; S Murphy; T A Donlon
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2001-12       Impact factor: 4.254

5.  The relationship between riboflavin and plasma total homocysteine in the Framingham Offspring cohort is influenced by folate status and the C677T transition in the methylenetetrahydrofolate reductase gene.

Authors:  Paul F Jacques; Renee Kalmbach; Pamela J Bagley; Giuseppina T Russo; Gail Rogers; Peter W F Wilson; Irwin H Rosenberg; Jacob Selhub
Journal:  J Nutr       Date:  2002-02       Impact factor: 4.798

6.  Methylenetetrahydrofolate reductase (MTHFR) polymorphism increases the risk of cervical intraepithelial neoplasia.

Authors:  C J Piyathilake; M Macaluso; G L Johanning; M Whiteside; D C Heimburger; A Giuliano
Journal:  Anticancer Res       Date:  2000 May-Jun       Impact factor: 2.480

7.  ASCUS-LSIL Triage Study. Design, methods and characteristics of trial participants.

Authors:  M Schiffman; M E Adrianza
Journal:  Acta Cytol       Date:  2000 Sep-Oct       Impact factor: 2.319

8.  Women with polymorphisms of methylenetetrahydrofolate reductase (MTHFR) and methionine synthase (MS) are less likely to have cervical intraepithelial neoplasia (CIN) 2 or 3.

Authors:  Olga L Henao; Chandrika J Piyathilake; John W Waterbor; Ellen Funkhouser; Gary L Johanning; Douglas C Heimburger; Edward E Partridge
Journal:  Int J Cancer       Date:  2005-03-01       Impact factor: 7.396

9.  Impaired functioning of thermolabile methylenetetrahydrofolate reductase is dependent on riboflavin status: implications for riboflavin requirements.

Authors:  Helene McNulty; Michelle C McKinley; Barbara Wilson; Joseph McPartlin; J J Strain; Donald G Weir; John M Scott
Journal:  Am J Clin Nutr       Date:  2002-08       Impact factor: 7.045

10.  Effect of riboflavin status on the homocysteine-lowering effect of folate in relation to the MTHFR (C677T) genotype.

Authors:  Stuart J Moat; Pauline A L Ashfield-Watt; Hilary J Powers; Robert G Newcombe; Ian F W McDowell
Journal:  Clin Chem       Date:  2003-02       Impact factor: 8.327

View more
  7 in total

1.  MTHFR C677T polymorphism contributes to colorectal cancer susceptibility: evidence from 61 case-control studies.

Authors:  Xuewen Sheng; Yanxi Zhang; Erjiang Zhao; Su Lu; Xiaoli Zheng; Hong Ge; Weiquan Lu
Journal:  Mol Biol Rep       Date:  2012-06-23       Impact factor: 2.316

2.  MTHFR C677T and A1298C polymorphisms and cervical carcinoma susceptibility: meta-analyses based on 4,421 individuals.

Authors:  Wen-Lei Zhuo; Liang Zhang; Jun-Jun Ling; Yi Zhu; Zheng-Tang Chen
Journal:  Mol Biol Rep       Date:  2012-06-19       Impact factor: 2.316

Review 3.  A literature review of MTHFR (C677T and A1298C polymorphisms) and cancer risk.

Authors:  Muzeyyen Izmirli
Journal:  Mol Biol Rep       Date:  2012-10-19       Impact factor: 2.316

4.  Methylenetetrahydrofolate reductase (MTHFR) polymorphisms and susceptibility for cervical lesions: a meta-analysis.

Authors:  Shuyu Long; Xingliang Yang; Xiaojiao Liu; Pei Yang
Journal:  PLoS One       Date:  2012-12-21       Impact factor: 3.240

5.  A comprehensive review on host genetic susceptibility to human papillomavirus infection and progression to cervical cancer.

Authors:  Koushik Chattopadhyay
Journal:  Indian J Hum Genet       Date:  2011-09

6.  Lack of association between methylenetetrahydrofolate reductase C677T polymorphism, HPV infection and cervical intraepithelial neoplasia in Brazilian women.

Authors:  Nayara Nascimento Toledo Silva; Adriano de Paula Sabino; Alexandre Tafuri; Angélica Alves Lima
Journal:  BMC Med Genet       Date:  2019-06-06       Impact factor: 2.103

7.  Association of the plasma and tissue riboflavin levels with C20orf54 expression in cervical lesions and its relationship to HPV16 infection.

Authors:  Aixingzi Aili; Ayshamgul Hasim; Alimujiang Kelimu; Xia Guo; Batur Mamtimin; Abuliz Abudula; Halmurat Upur
Journal:  PLoS One       Date:  2013-11-18       Impact factor: 3.240

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.