التفاصيل البيبلوغرافية
| العنوان: |
A Heritable Missense Polymorphism in CDKN2A Confers Strong Risk of Childhood Acute Lymphoblastic Leukemia and Is Preferentially Selected during Clonal Evolution. |
| المؤلفون: |
Walsh, Kyle M.1 kyle.walsh@ucsf.edu, de Smith, Adam J.2, Hansen, Helen M.1, Smirnov, Ivan V.1, Gonseth, Semira2, Endicott, Alyson A.2, Jianqiao Xiao2, Rice, Terri1, Fu, Cecilia H.3, McCoy, Lucie S.1, Lachance, Daniel H.4, Eckel-Passow, Jeanette E.5, Wiencke, John K.1,6, Jenkins, Robert B.7, Wrensch, Margaret R.1,6, Xiaomei Ma8, Metayer, Catherine9, Wiemels, Joseph L.1,2,6 |
| المصدر: |
Cancer Research. 11/15/2015, Vol. 75 Issue 22, p4884-4894. 11p. |
| مصطلحات موضوعية: |
*HERITABILITY, *MISSENSE mutation, *GENETIC polymorphisms, *CYCLIN-dependent kinase inhibitor-2A, *LYMPHOBLASTIC leukemia, *BIOLOGICAL evolution |
| مستخلص: |
Genome-wide association studies (GWAS) have identified SNPs in six genes that are associated with childhood acute lymphoblastic leukemia (ALL). A lead SNP was found to occur on chromosome 9p21.3, a region that is deleted in 30% of childhood ALLs, suggesting the presence of causal polymorphisms linked to ALL risk. We used SNP genotyping and imputation-based fine-mapping of a multiethnic ALL case-control population (Ncases = 1,464, Ncontrols = 3,279) to identify variants of large effect within 9p21.3. We identified a CDKN2A missense variant (rs3731249) with 2% allele frequency in controls that confers three-fold increased risk of ALL in children of European ancestry (OR, 2.99; P = 1.51 x 10-9) and Hispanic children (OR, 2.77; P = 3.78 x 10-4). Moreover, of 17 patients whose tumors displayed allelic imbalance at CDKN2A, 14 preferentially retained the risk allele and lost the protective allele (PBinomial = 0.006), suggesting that the risk allele provides a selective advantage during tumor growth. Notably, the CDKN2A variant was not significantly associated with melanoma, glioblastoma, or pancreatic cancer risk, implying that this polymorphism specifically confers ALL risk but not general cancer risk. Taken together, our findings demonstrate that coding polymorphisms of large effect can underlie GWAS "hits" and that inherited polymorphisms may undergo directional selection during clonal expansion of tumors. [ABSTRACT FROM AUTHOR] |
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