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Blood ; 120(4): 843-6, 2012 Jul 26.
Article in English | MEDLINE | ID: mdl-22700719

ABSTRACT

We performed a meta-analysis of 3 genome-wide association studies to identify additional common variants influencing chronic lymphocytic leukemia (CLL) risk. The discovery phase was composed of genome-wide association study data from 1121 cases and 3745 controls. Replication analysis was performed in 861 cases and 2033 controls. We identified a novel CLL risk locus at 6p21.33 (rs210142; intronic to the BAK1 gene, BCL2 antagonist killer 1; P = 9.47 × 10(-16)). A strong relationship between risk genotype and reduced BAK1 expression was shown in lymphoblastoid cell lines. This finding provides additional support for polygenic inheritance to CLL and provides further insight into the biologic basis of disease development.


Subject(s)
Antineoplastic Agents/adverse effects , Chromosome Aberrations/chemically induced , Leukemia, Myeloid, Chronic-Phase/drug therapy , Leukemia, Myeloid, Chronic-Phase/genetics , Philadelphia Chromosome , Piperazines/adverse effects , Pyrimidines/adverse effects , Adolescent , Adult , Aged , Aged, 80 and over , Benzamides , Cytogenetic Analysis , Female , Humans , Imatinib Mesylate , In Situ Hybridization, Fluorescence , Leukemia, Myeloid, Chronic-Phase/mortality , Male , Middle Aged , Prognosis , Prospective Studies , RNA, Messenger/genetics , Real-Time Polymerase Chain Reaction , Reverse Transcriptase Polymerase Chain Reaction , Survival Rate , Young Adult
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