Association of ARID5B gene variants with acute lymphoblastic leukemia in Yemeni children

被引:11
作者
Al-absi, Boshra [1 ]
Noor, Suzita M. [2 ]
Saif-Ali, Riyadh [3 ]
Salem, Sameer D. [3 ]
Ahmed, Radwan H. [1 ]
Razif, Muhammad F. M. [1 ]
Muniandy, Sekaran [1 ]
机构
[1] Univ Malaya, Fac Med, Dept Mol Med, Kuala Lumpur 50603, Malaysia
[2] Univ Malaya, Fac Med, Dept Biomed Sci, Kuala Lumpur, Malaysia
[3] Sanaa Univ, Fac Med, Dept Biochem & Mol Biol, Sanaa, Yemen
关键词
Childhood leukemia; ARID5B; single nucleotide polymorphism; haplotype; genotyping; SUSCEPTIBILITY LOCI; RACIAL-DIFFERENCES; CHILDHOOD; RISK; 10Q21.2; 7P12.2; IKZF1; POLYMORPHISMS; 14Q11.2; CEBPE;
D O I
10.1177/1010428317697573
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Studies have shown an association between ARID5B gene polymorphisms and childhood acute lymphoblastic leukemia. However, the association between ARID5B variants and acute lymphoblastic leukemia among the Arab population still needs to be studied. The aim of this study was to investigate the association between ARID5B variants with acute lymphoblastic leukemia in Yemeni children. A total of 14 ARID5B gene single nucleotide polymorphisms (SNPs) were genotyped in 289 Yemeni children, of whom 136 had acute lymphoblastic leukemia and 153 were controls, using the nanofluidic Dynamic Array (Fluidigm 192.24 Dynamic Array). Using logistic regression adjusted for age and gender, the risks of acute lymphoblastic leukemia were presented as odds ratios and 95% confidence intervals. We found that nine SNPs were associated with acute lymphoblastic leukemia under additive genetic models: rs7073837, rs10740055, rs7089424, rs10821936, rs4506592, rs10994982, rs7896246, rs10821938, and rs7923074. Furthermore, the recessive models revealed that six SNPs were risk factors for acute lymphoblastic leukemia: rs10740055, rs7089424, rs10994982, rs7896246, rs10821938, and rs7923074. The gender-specific impact of these SNPs under the recessive genetic model revealed that SNPs rs10740055, rs10994982, and rs6479779 in females, and rs10821938 and rs7923074 in males were significantly associated with acute lymphoblastic leukemia risk. Under the dominant model, SNPs rs7073837, rs10821936, rs7896246, and rs6479778 in males only showed striking association with acute lymphoblastic leukemia. The additive model revealed that SNPs with significant association with acute lymphoblastic leukemia were rs10821936 (both males and females); rs7073837, rs10740055, rs10994982, and rs4948487 (females only); and rs7089424, rs7896246, rs10821938, and rs7923074 (males only). In addition, the ARID5B haplotype block (CGAACACAA) showed a higher risk for acute lymphoblastic leukemia. The haplotype (CCCGACTGC) was associated with protection against acute lymphoblastic leukemia. In conclusion, our study has shown that ARID5B variants are associated with acute lymphoblastic leukemia in Yemeni children with several gender biases of ARID5B single nucleotide polymorphisms reported.
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页数:8
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共 36 条
[1]  
[Anonymous], 2012, Globocan 2012: Estimated cancer incidence, mortality and prevalence worldwide in 2012
[2]   Childhood cancer in Aden, Yemen [J].
Ba-Saddik, Iman Ali .
CANCER EPIDEMIOLOGY, 2013, 37 (06) :803-806
[3]   Influence of genetic polymorphisms on the risk of developing leukemia and on disease progression [J].
Bolufer, Pascual ;
Barragan, Eva ;
Collado, Maria ;
Cervera, Jose ;
Lopez, Jose-Antonio ;
Sanz, Miguel A. .
LEUKEMIA RESEARCH, 2006, 30 (12) :1471-1491
[4]   Genetic variants in ARID5B and CEBPE are childhood ALL susceptibility loci in Hispanics [J].
Chokkalingam, Anand P. ;
Hsu, Ling-I ;
Metayer, Catherine ;
Hansen, Helen M. ;
Month, Stacy R. ;
Barcellos, Lisa F. ;
Wiemels, Joseph L. ;
Buffler, Patricia A. .
CANCER CAUSES & CONTROL, 2013, 24 (10) :1789-1795
[5]   Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia [J].
Ellinghaus, E. ;
Stanulla, M. ;
Richter, G. ;
Ellinghaus, D. ;
Kronnie, G. Te ;
Cario, G. ;
Cazzaniga, G. ;
Horstmann, M. ;
Gruemayer, R. Panzer ;
Cave, H. ;
Trka, J. ;
Cinek, O. ;
Teigler-Schlegel, A. ;
ElSharawy, A. ;
Haesler, R. ;
Nebel, A. ;
Meissner, B. ;
Bartram, T. ;
Lescai, F. ;
Franceschi, C. ;
Giordan, M. ;
Nuernberg, P. ;
Heinzow, B. ;
Zimmermann, M. ;
Schreiber, S. ;
Schrappe, M. ;
Franke, A. .
LEUKEMIA, 2012, 26 (05) :902-909
[6]   In utero origins of childhood leukaemia [J].
Greaves, M .
EARLY HUMAN DEVELOPMENT, 2005, 81 (01) :123-129
[7]   Clonal evolution in cancer [J].
Greaves, Mel ;
Maley, Carlo C. .
NATURE, 2012, 481 (7381) :306-313
[8]   ARID5B gene rs10821936 polymorphism is associated with childhood acute lymphoblastic leukemia: a meta-analysis based on 39,116 subjects [J].
Guo, Lei-Ming ;
Xi, Jia-Shui ;
Ma, Yan ;
Shao, Lin ;
Nie, Cui-Li ;
Wang, Guang-Jun .
TUMOR BIOLOGY, 2014, 35 (01) :709-713
[9]   Intron 3 of the ARID5B gene: a hot spot for acute lymphoblastic leukemia susceptibility [J].
Gutierrez-Camino, Angela ;
Lopez-Lopez, Elixabet ;
Martin-Guerrero, Idoia ;
Sanchez-Toledo, Jose ;
Garcia de Andoin, Nagore ;
Carbone Baneres, Ana ;
Garcia-Miguel, Purificacion ;
Navajas, Aurora ;
Garcia-Orad, Africa .
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 2013, 139 (11) :1879-1886
[10]   Genome-wide association study of childhood acute lymphoblastic leukemia in Korea [J].
Han, Sohee ;
Lee, Kyoung-Mu ;
Park, Sue K. ;
Lee, Jong Eun ;
Ahn, Hyo Seop ;
Shin, Hee Young ;
Kang, Hyoung Jin ;
Koo, Hong Hoe ;
Seo, Jong Jin ;
Choi, Ji Eun ;
Ahn, Yoon-Ok ;
Kang, Daehee .
LEUKEMIA RESEARCH, 2010, 34 (10) :1271-1274