References
- Bhandari P, Ahmad F, Dalvi R, et al (2015). Cytogenetic Profile of De Novo B lineage Acute Lymphoblastic Leukemia: Determination of Frequency, Distribution Pattern and Identification of Rare and Novel Chromosomal Aberrations in Indian Patients. Asian Pac J Cancer Prev, 16, 7219-29. https://doi.org/10.7314/APJCP.2015.16.16.7219
- Chokkalingam AP, Hsu L-I, Metayer C, et al (2013). Genetic variants in ARID5B and CEBPE are childhood ALL susceptibility loci in Hispanics. Cancer Causes Control, 24, 1789-95. https://doi.org/10.1007/s10552-013-0256-3
- Dai Y, Tang L, Healy J, Sinnett D (2014). Contribution of Polymorphisms in IKZF1 Gene to Childhood Acute Leukemia: A Meta-Analysis of 33 Case-Control Studies. PLoS ONE, 9, 113748. https://doi.org/10.1371/journal.pone.0113748
- Ellinghaus E, Stanulla M, Richter G, et al (2012). Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic. Leukemia, 26, 902-9. https://doi.org/10.1038/leu.2011.302
- Fletcher O, Houlston RS (2010). Architecture of inherited susceptibility to common cancer. Nat Rev Cancer, 10, 353-61. https://doi.org/10.1038/nrc2840
- Georgopoulos K, Bigby M, Wang J-H, et al (1994). The ikaros gene is required for the development of all lymphoid lineages. Cell, 79, 143-56. https://doi.org/10.1016/0092-8674(94)90407-3
- Gutierrez-Camino A, Lopez-Lopez E, Martin-Guerrero I, et al (2013). Intron 3 of the ARID5B gene: a hot spot for acute lymphoblastic leukemia susceptibility. J Cancer Res Clin Oncol, 139, 1879-86. https://doi.org/10.1007/s00432-013-1512-3
- Han S, Lee K-M, Park SK, et al (2010). Genome-wide association study of childhood acute lymphoblastic leukemia in Korea. Leuk Res, 34, 1271-4. https://doi.org/10.1016/j.leukres.2010.02.001
- Healy J, Richer C, Bourgey M, Kritikou EA, Sinnett D (2010). Replication analysis confirms the association of ARID5B with childhood B-cell acute lymphoblastic leukemia. Haematologica, 95, 1608-11. https://doi.org/10.3324/haematol.2010.022459
- Jiang Y, Hou J, Zhang Q, et al (2013). The MTHFR C677T polymorphism and risk of acute lymphoblastic leukemia: an updated meta-analysis based on 37 case-control studies. Asian Pac J Cancer Prev, 14, 6357-62. https://doi.org/10.7314/APJCP.2013.14.11.6357
- Kennedy AE, Kamdar KY, Lupo PJ, et al (2015). Genetic markers in a multi-ethnic sample for childhood acute lymphoblastic leukemia risk. Leuk Lymphoma, 56, 169-74. https://doi.org/10.3109/10428194.2014.910662
- Kreile M, Rots D, Piekuse L, et al (2014). Lack of association between polymorphisms in genes MTHFR and MDR1 with risk of childhood acute lymphoblastic leukemia. Asian Pac J Cancer Prev, 15, 9707-11. https://doi.org/10.7314/APJCP.2014.15.22.9707
- Lautner-Csorba O, Gezsi A, Semsei AF, et al (2012). Candidate gene association study in pediatric acute lymphoblastic leukemia evaluated by Bayesian network based Bayesian multilevel analysis of relevance. BMC Med Genomics, 5, 1-15. https://doi.org/10.1186/1755-8794-5-1
- Li S, Ren L, Fan L, Wang G (2014). IKZF1 rs4132601 polymorphism and acute lymphoblastic leukemia susceptibility: a meta-analysis. Leuk Lymphoma, 56, 1-13.
- Lin C, Song W, Bi X, et al (2014a). Recent advances in the ARID family: focusing on roles in human cancer. OncoTargets Ther, 7, 315-24.
- Lin C-Y, Li M-J, Chang J-G, et al (2014b). High-resolution melting analyses for genetic variants in ARID5B and IKZF1 with childhood acute lymphoblastic leukemia susceptibility loci in Taiwan. Blood Cells Mol Dis, 52, 140-5. https://doi.org/10.1016/j.bcmd.2013.10.003
- Mullighan CG, Su X, Zhang J, et al (2009). Deletion of IKZF1 and prognosis in acute lymphoblastic leukemia. N Engl J Med, 360, 470-80. https://doi.org/10.1056/NEJMoa0808253
- Orsi L, Rudant J, Bonaventure A, et al (2012). Genetic polymorphisms and childhood acute lymphoblastic leukemia: GWAS of the ESCALE study (SFCE). Leukemia, 26, 2561-4. https://doi.org/10.1038/leu.2012.148
-
Pan Y, Chen H, Liang H, Wang X, Wang L (2014). Meta-analysis of the association between CCAAT/enhancer binding protein-
$\varepsilon$ polymorphism and the risk of childhood acute lymphoblastic leukemia. Int J Clin Exp Med, 7, 5553-7. - Papaemmanuil E, Hosking FJ, Vijayakrishnan J, et al (2009). Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia. Nat Genet, 41, 1006-10. https://doi.org/10.1038/ng.430
- Pastorczak A, Gorniak P, Sherborne A, et al (2011). Role of 657del5 NBN mutation and 7p12.2 (IKZF1), 9p21 (CDKN2A), 10q21.2 (ARID5B) and 14q11.2 (CEBPE) variation and risk of childhood ALL in the Polish population. Leuk Res, 35, 1534-6. https://doi.org/10.1016/j.leukres.2011.07.034
- Pongstaporn W, Pakakasama S, Chaksangchaichote P, et al (2015). MDR1 C3435T and C1236T polymorphisms: association with high-risk childhood acute lymphoblastic leukemia. Asian Pac J Cancer Prev, 16, 2839-43. https://doi.org/10.7314/APJCP.2015.16.7.2839
- Prasad RB, Hosking FJ, Vijayakrishnan J, et al (2010). Verification of the susceptibility loci on 7p12.2, 10q21.2, and 14q11.2 in precursor B-cell acute lymphoblastic leukemia of childhood. Blood, 115, 1765-7. https://doi.org/10.1182/blood-2009-09-241513
- Sole X, Guino E, Valls J, Iniesta R, Moreno V (2006). SNPStats: a web tool for the analysis of association studies. Bioinformatics, 22, 1928-9. https://doi.org/10.1093/bioinformatics/btl268
- Trevino LR, Yang W, French D, et al (2009). Germline genomic variants associated with childhood acute lymphoblastic leukemia. Nat Genet, 41, 1001-5. https://doi.org/10.1038/ng.432
- Vijayakrishnan J, Sherborne AL, Sawangpanich R, et al (2010). Variation at 7p12.2 and 10q21.2 influences childhood acute lymphoblastic leukemia risk in the Thai population and may contribute to racial differences in leukemia incidence. Leuk Lymphoma, 51, 1870-4. https://doi.org/10.3109/10428194.2010.511356
- Walsh KM, Chokkalingam AP, Hsu L-I, et al (2013). Associations between genome-wide Native American ancestry, known risk alleles and B-cell ALL risk in Hispanic children. Leukemia, 27, 2416-9. https://doi.org/10.1038/leu.2013.130
- Wang Y, Chen J, Li J, et al (2013). Association of three polymorphisms in ARID5B, IKZF1and CEBPE with the risk of childhood acute lymphoblastic leukemia in a Chinese population. Gene, 524, 203-7. https://doi.org/10.1016/j.gene.2013.04.028
- Xu H, Cheng C, Devidas M, et al (2012). ARID5B Genetic Polymorphisms Contribute to Racial Disparities in the Incidence and Treatment Outcome of Childhood Acute Lymphoblastic Leukemia. J Clin Oncol, 30, 751-7. https://doi.org/10.1200/JCO.2011.38.0345
- Yadav SP, Rastogi N, Kharya G, et al (2014). Barriers to Cure for children with cancer in india and strategies to improve outcomes: a report by the indian pediatric hematology oncology group. Pediatr Hematol Oncol, 31, 217-24. https://doi.org/10.3109/08880018.2014.893596
- Yang W, Trevino LR, Yang JJ, et al (2010). ARID5B SNP rs10821936 is associated with risk of childhood acute lymphoblastic leukemia in blacks and contributes to racial differences in leukemia incidence. Leukemia, 24, 894-6. https://doi.org/10.1038/leu.2009.277
- Zeng H, Wang XB, Cui NH, et al (2014). Associations between AT-rich Interactive Domain 5B gene Polymorphisms and Risk of Childhood Acute Lymphoblastic Leukemia: a Metaanalysis. Asian Pac J Cancer Prev, 15, 6211-7. https://doi.org/10.7314/APJCP.2014.15.15.6211