Genome-Wide SNP Analysis in Cancer: Leukemia Shows the Way

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Genome-Wide SNP Analysis in Cancer: Leukemia Shows the Way Yingzi Wang, Scott A. Armstrong  Cancer Cell  Volume 11, Issue 4, Pages 308-309 (April 2007) DOI: 10.1016/j.ccr.2007.03.017 Copyright © 2007 Elsevier Inc. Terms and Conditions

Figure 1 SNP Analysis of B-ALL Identifies Recurrent Mutations in Genes Important for Normal B Cell Development Mullighan et al. analyzed 242 pediatric ALL cases using genome-wide SNP analysis. Recurrent deletions in B-precursor ALL samples were identified in genes such as EBF1 and PAX5 that are known regulators of B cell development. This suggests that perturbation of normal pathways that promote development from common lymphoid progenitors (CLP) to pre-B cells is an important part of the pathogenesis of B-ALL and highlights the power of genome-wide assessment of cancer cells. Cancer Cell 2007 11, 308-309DOI: (10.1016/j.ccr.2007.03.017) Copyright © 2007 Elsevier Inc. Terms and Conditions