Access the full text.
Sign up today, get DeepDyve free for 14 days.
K. Jaskiewicz, Marasas Wf, C. Lazarus, Beyers Ad, Van Pd (1988)
Association of esophageal cytological abnormalities with vitamin and lipotrope deficiencies in populations at risk for esophageal cancer.Anticancer research, 8 4
S. Weinstein, G. Gridley, L. Harty, S. Diehl, L. Brown, D. Winn, Eleuterio Bravo-Otero, R. Hayes (2002)
Folate intake, serum homocysteine and methylenetetrahydrofolate reductase (MTHFR) C677T genotype are not associated with oral cancer risk in Puerto Rico.The Journal of nutrition, 132 4
Chunying Song, Deyin Xing, W. Tan, Qingyi Wei, D. Lin (2001)
Methylenetetrahydrofolate reductase polymorphisms increase risk of esophageal squamous cell carcinoma in a Chinese population.Cancer research, 61 8
Yi-Lin Jeng, Mei-Hsuan Wu, Han-Bin Huang, Wei-Yu Lin, S. You, T. Chu, Chien-Jen Chen, Chien‐An Sun (2003)
The methylenetetrahydrofolate reductase 677C-->T polymorphism and lung cancer risk in a Chinese population.Anticancer research, 23 6D
M. Tseng, S. Murray, L. Kupper, R. Sandler (1996)
Micronutrients and the risk of colorectal adenomas.American journal of epidemiology, 144 11
H. Pauer, T. Voigt-Tschirschwitz, B. Hinney, P. Burfeind, Cornelia Wolf, G. Emons, J. Neesen (2003)
Analyzes of three common thrombophilic gene mutations in German women with recurrent abortionsActa Obstetricia et Gynecologica Scandinavica, 82
Robert Kim, R. Becker (2003)
Association between factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations and events of the arterial circulatory system: a meta-analysis of published studies.American heart journal, 146 6
T. Antoniadi, T. Hatzis, C. Kroupis, E. Economou-Petersen, M. Petersen (1999)
Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in a Greek population of blood donors.American journal of hematology, 61 4
L. Meglič, M. Stegnar, T. Milanez, M. Božič, B. Peterlin, P. Peternel, Z. Novak-Antolic (2003)
Factor V Leiden, prothrombin 20210G --> A, methylenetetrahydrofolate reductase 677C --> T and plasminogen activator inhibitor 4G/5G polymorphism in women with pregnancy-related venous thromboembolism.European journal of obstetrics, gynecology, and reproductive biology, 111 2
Nicole Dowling, H. Austin, A. Dilley, C. Whitsett, B. Evatt, W. Hooper (2003)
The epidemiology of venous thromboembolism in Caucasians and African‐Americans: the GATE Study 1Journal of Thrombosis and Haemostasis, 1
L. Brattström, D. Wilcken, J. Öhrvik, L. Brudin (1998)
Common methylenetetrahydrofolate reductase gene mutation leads to hyperhomocysteinemia but not to vascular disease: the result of a meta-analysis.Circulation, 98 23
R. Stolzenberg-Solomon, Y. Qiao, C. Abnet, D. Ratnasinghe, S. Dawsey, Z. Dong, P. Taylor, S. Mark (2003)
Esophageal and gastric cardia cancer risk and folate- and vitamin B(12)-related polymorphisms in Linxian, China.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 12 11 Pt 1
V. Gudnason, D. Stansbie, J. Scott, A. Bowron, V. Nicaud, S. Humphries (1997)
C677T (thermolabile alanine/valine) polymorphism in methylenetetrahydrofolate reductase (MTHFR): its frequency and impact on plasma homocysteine concentration in different European populations. EARS group.Atherosclerosis, 136 2
P. Frosst, H. Blom, R. Milos, P. Goyette, C. Sheppard, R. Matthews, G. Boers, M. Heijer, L. Kluijtmans, L. Heuve, R. Rozen (1995)
A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductaseNature Genetics, 10
K. Sohn, R. Croxford, Z. Yates, M. Lucock, Young-In Kim (2004)
Effect of the methylenetetrahydrofolate reductase C677T polymorphism on chemosensitivity of colon and breast cancer cells to 5-fluorouracil and methotrexate.Journal of the National Cancer Institute, 96 2
E. Vairaktaris, C. Yapijakis, J. Wiltfang, J. Ries, A. Vylliotis, S. Derka, Stavros Vasiliou, F. Neukam (2005)
Are factor V and prothrombin mutations associated with increased risk of oral cancer?Anticancer research, 25 3c
K. Siemianowicz, J. Gmiński, W. Garczorz, Natalia Slabiak, M. Goss, M. Machalski, H. Magiera-Molendowska (2003)
Methylenetetrahydrofolate reductase gene C677T and A1298C polymorphisms in patients with small cell and non-small cell lung cancer.Oncology reports, 10 5
P. Isotalo, J. Donnelly (2002)
Comment on ‘increased frequency of combined methylenetetrahydrofolate reductase C677T and A1298C mutated alleles in spontaneously aborted embryos’European Journal of Human Genetics, 10
H. Zetterberg, B. Regland, M. Palmér, A. Ricksten, L. Palmqvist, L. Rymo, D. Arvanitis, D. Spandidos, K. Blennow (2002)
Increased frequency of combined methylenetetrahydrofolate reductase C677T and A1298C mutated alleles in spontaneously aborted embryosEuropean Journal of Human Genetics, 10
U. Nowak-Göttl, C. Wermes, R. Junker, H. Koch, R. Schobess, G. Fleischhack, D. Schwabe, S. Ehrenforth (1999)
Prospective evaluation of the thrombotic risk in children with acute lymphoblastic leukemia carrying the MTHFR TT 677 genotype, the prothrombin G20210A variant, and further prothrombotic risk factors.Blood, 93 5
E. Giovannucci, E. Rimm, A. Ascherio, M. Stampfer, G. Colditz, W. Willett (1995)
Alcohol, low-methionine--low-folate diets, and risk of colon cancer in men.Journal of the National Cancer Institute, 87 4
P. Jacques, A. Bostom, Roger Williams, R. Ellison, J. Eckfeldt, I. Rosenberg, J. Selhub, R. Rozen (1996)
Relation between folate status, a common mutation in methylenetetrahydrofolate reductase, and plasma homocysteine concentrations.Circulation, 93 1
L. Bailey (2003)
Folate, methyl-related nutrients, alcohol, and the MTHFR 677C-->T polymorphism affect cancer risk: intake recommendations.The Journal of nutrition, 133 11 Suppl 1
E. Ramacciotti, N. Wolosker, P. Puech-Leão, Eduardo Zeratti, Paula Gusson, A. Giglio, R. Franco (2003)
Prevalence of factor V Leiden, FII G20210A, FXIII Val34Leu and MTHFR C677T polymorphisms in cancer patients with and without venous thrombosis.Thrombosis research, 109 4
R. Pihusch, G. Danzl, M. Scholz, Detlev Harich, M. Pihusch, P. Lohse, E. Hiller (2002)
Impact of thrombophilic gene mutations on thrombosis risk in patients with gastrointestinal carcinomaCancer, 94
P. Isotalo, G. Wells, J. Donnelly, J. Donnelly (2000)
Neonatal and fetal methylenetetrahydrofolate reductase genetic polymorphisms: an examination of C677T and A1298C mutations.American journal of human genetics, 67 4
M. Krajinovic, Stéphanie Lamothe, D. Labuda, É. Lemieux-Blanchard, Y. Théorêt, A. Moghrabi, D. Sinnett (2004)
Role of MTHFR genetic polymorphisms in the susceptibility to childhood acute lymphoblastic leukemia.Blood, 103 1
Ilan Weisberg, P. Tran, B. Christensen, Sahar Sibani, R. Rozen (1998)
A second genetic polymorphism in methylenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity.Molecular genetics and metabolism, 64 3
(2003)
Methylenetetrahydrofolate reductase 677CC normal genotype may protect against multiple myeloma
Sang-Woon Choi, J. Mason (2000)
Folate and carcinogenesis: an integrated scheme.The Journal of nutrition, 130 2
Purpose: We investigated whether the mutant methylenetetrahydrofolate reductase (MTHFR) increases risk for oral cancer. The common germ-line mutation C677T in the MTHFR gene significantly diminishes specific activity of the enzyme, which is responsible for the circulating form of folate. Folate deficiency is associated with increased risk for thrombosis, as well as for several types of cancer, through disruption of DNA methylation, DNA synthesis and deficient DNA repair. Methods: We searched for the C677T mutation by restriction fragment analysis of PCR products in DNA samples of 110 patients with oral squamous cell carcinoma and 120 healthy controls of comparable ethnicity, age and sex. Results: The number of heterozygotes was significantly different in the two groups (P<0.005), as well as in subgroups of patients with or without a positive family history for cancer, compared to normal controls (P<0.01 and P<0.005, respectively). Furthermore, the subgroup of patients with a positive family history for thrombophilia had a significant increase both in the frequencies of mutant alleles (P<0.01) and heterozygotes (P<0.001) in comparison to normal controls. Conclusions: The obtained results suggest that the MTHFR mutation is a minor contributing factor in oncogenesis in the oral region, in conjunction with low dietary uptake of folate.
Journal of Cancer Research and Clinical Oncology – Springer Journals
Published: Dec 20, 2005
Read and print from thousands of top scholarly journals.
Already have an account? Log in
Bookmark this article. You can see your Bookmarks on your DeepDyve Library.
To save an article, log in first, or sign up for a DeepDyve account if you don’t already have one.
Copy and paste the desired citation format or use the link below to download a file formatted for EndNote
Access the full text.
Sign up today, get DeepDyve free for 14 days.
All DeepDyve websites use cookies to improve your online experience. They were placed on your computer when you launched this website. You can change your cookie settings through your browser.