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Association of the 5,10-methylenetetrahydrofolate reductase (MTHFR C677T and A1298C) polymorphisms in koreanpatients with adupatients with adult acute lymphoblastic leukemia

Authors
 DOYEUN OH  ;  NAM KEUN KIM  ;  YOO HONG MIN  ;  HYUN SOOK CHI  ;  SEONYANG PARK  ;  HEUNG SIK KIM  ;  CHUL SOO KIM  ;  MYUNG JU AHN  ;  JUNG AE LEE  ;  JAE HOON LEE  ;  HUGH CHUL KIM  ;  MOON JU JANG 
Citation
 ANTICANCER RESEARCH, Vol.27(5A) : 3419-3424, 2007 
Journal Title
ANTICANCER RESEARCH
ISSN
 0250-7005 
Issue Date
2007
Abstract
BACKGROUND:
Methylenetetrahydrofolate reductase (MTHFR) plays a central role in converting folate to methyl donor for DNA methylation. Because MTHFR is a key enzyme in folate metabolism, changes in its activity resulting from polymorphisms in the MTHFR gene could modify the susceptibility to cancer. Recently, the C677T and A1298C mutations of MTHFR were discovered to be associated with susceptibility in acute lymphoblastic leukemia (ALL).
PATIENTS AND METHODS:
The association between MTHFR polymorphisms and susceptibility and clinical outcome in ALL was studied in 118 adult ALL patients and matched healthy controls (n =427). DNA samples taken from patients with ALL and controls were analyzed using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) assays to detect the MTHFR C677T and A1298C mutations.
RESULTS:
No significant difference was found in the development of adult ALL among those with different MTHFR genotypes of the C677T or A1298C polymorphisms. However, the MTHFR 677CT+TT genotype showed a tendency to be associated with adult ALL [crude odds ratio (OR), 0.67; 95% confidence interval (CI), 0.44-1.02; adjusted OR, 0.74 95% CI, 0.47-1.14].
CONCLUSION:
The MTHFR C677T and A1298C polymorphisms are not significant risk factors in adult acute leukemia in the Korean population.
Files in This Item:
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Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Min, Yoo Hong(민유홍) ORCID logo https://orcid.org/0000-0001-8542-9583
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/95639
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