MTHFR 677CT And 1298AC POLYMORPHISMS IN CHILDREN WITH DOWN SYNDROME AND ACUTE MYELOID LEUKEMIA IN BRAZIL

被引:7
作者
Amorim, Marcia R. [1 ]
Zanrosso, Crisiane Wais
Magalhaes, Isis Q. [2 ,3 ]
Pereira, Simone C. [3 ]
Figueiredo, Alexandre
Emerenciano, Mariana
Pinheiro, Vitoria Regia [4 ]
d'Andrea, Maria Lydia [5 ]
Orioli, Ieda M. [6 ]
Koifman, Sergio [7 ]
Pombo-de-Oliveira, Maria. S.
机构
[1] Inst Nacl Canc, Res Ctr Expt Med, Pediat Hematol Oncol Program, BR-20231050 Rio De Janeiro, Brazil
[2] Hosp Apoio Brasilia, Brasilia, DF, Brazil
[3] Inst Nacl Canc, Div Expt Med, Rio De Janeiro, Brazil
[4] Ctr Infantil Boldrini, Campinas, SP, Brazil
[5] Hosp Darcy Vargas, Dept Pediat Oncol, Sao Paulo, Brazil
[6] Univ Fed Do, Inst Biol, Dept Genet, Rio De Janeiro, Brazil
[7] Fiocruz MS, Escola Nacl Saude Publ, BR-21045900 Rio De Janeiro, Brazil
关键词
677CT; 1298AC; acute leukemia; MTHFR; Down syndrome;
D O I
10.1080/08880010802435104
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Down syndrome (DS) is an important risk factor associated with acute leukemia (AL). The presence of polymorphisms that reduce 5,10-methylenetetrahydrofolate reductase (MTHFR) activity has been linked to the multifactorial leukemogenic process. The authors have conducted a study to test whether 677CT and/or 1298AC polymorphisms of MTHFR would play an additional role in susceptibility of acute myeloid leukemia (AML) in DS children. They also verified whether any polymorphism in the MTHFR gene was associated with the risk of DS. Genetic polymorphisms determination was carried out in 248 samples from healthy individuals as controls and a total of 115 DS children (65 without leukemia and 50 with AML). The present study failed to reveal any association between these polymorphisms and risk of AML in DS children. The data also indicate that MTHFR polymorphisms are not associated with risk of being a DS child.
引用
收藏
页码:744 / 750
页数:7
相关论文
共 18 条
[1]   CLONAL HEMATOLOGIC DISORDERS IN DOWN-SYNDROME - A REVIEW [J].
AVETLOISEAU, H ;
MECHINAUD, F ;
HAROUSSEAU, JL .
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 1995, 17 (01) :19-24
[2]  
BAIN B, 1997, LEUKAEMIA DIAGNOSIS
[3]  
BENE MC, 1995, LEUKEMIA, V9, P1783
[4]  
Botto LD, 2000, AM J EPIDEMIOL, V151, P862
[5]   Methylenetetrahydrofolate reductase polymorphism in the etiology of down syndrome [J].
Chadefaux-Vekemans, B ;
Coudé, M ;
Muller, F ;
Oury, JF ;
Chabli, A ;
Jaïs, JP ;
Kamoun, P .
PEDIATRIC RESEARCH, 2002, 51 (06) :766-767
[6]   Association between the MTHFR A1298C polymorphism and increased risk of acute myeloid leukemia in Brazilian children [J].
Da Costa Ramos, Flavio Jose ;
De Mello, Maricilda Palandi ;
Yunes, Jose Andres ;
De Jesus Marques-Salles, Terezinha ;
Santos, Neide ;
Brandalise, Silvia R. ;
Pombo-de-Oliveira, Maria S. .
LEUKEMIA & LYMPHOMA, 2006, 47 (10) :2070-2075
[7]   Relationship between polymorphisms in genes involved in homocysteine metabolism and maternal risk for Down syndrome in Brazil [J].
da Silva, LRJ ;
Vergani, N ;
Galdieri, LD ;
Porto, MPR ;
Longhitano, SB ;
Brunoni, D ;
D'Almeida, V ;
Perez, ABA .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2005, 135A (03) :263-267
[8]   Origins of leukaemia in children with Down syndrome [J].
Hitzler, JK ;
Zipursky, A .
NATURE REVIEWS CANCER, 2005, 5 (01) :11-20
[9]   Polymorphisms in genes involved in folate metabolism as maternal risk factors for Down syndrome [J].
Hobbs, CA ;
Sherman, SL ;
Yi, P ;
Hopkins, SE ;
Torfs, CP ;
Hine, RJ ;
Pogribna, M ;
Rozen, R ;
James, SJ .
AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (03) :623-630
[10]  
LANGE K, 1997, BASIC PRINCIPLES POP