| Literature DB >> 18202291 |
Dengli Hong1, Rajeev Gupta, Philip Ancliff, Ann Atzberger, John Brown, Shamit Soneji, Joanne Green, Sue Colman, Wanda Piacibello, Veronica Buckle, Shinobu Tsuzuki, Mel Greaves, Tariq Enver.
Abstract
Understanding cancer pathogenesis requires knowledge of not only the specific contributory genetic mutations but also the cellular framework in which they arise and function. Here we explore the clonal evolution of a form of childhood precursor-B cell acute lymphoblastic leukemia that is characterized by a chromosomal translocation generating a TEL-AML1 fusion gene. We identify a cell compartment in leukemic children that can propagate leukemia when transplanted in mice. By studying a monochorionic twin pair, one preleukemic and one with frank leukemia, we establish the lineal relationship between these "cancer-propagating" cells and the preleukemic cell in which the TEL-AML1 fusion first arises or has functional impact. Analysis of TEL-AML1-transduced cord blood cells suggests that TEL-AML1 functions as a first-hit mutation by endowing this preleukemic cell with altered self-renewal and survival properties.Entities:
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Year: 2008 PMID： 18202291 DOI： 10.1126/science.1150648
Source DB: PubMed Journal: Science ISSN： 0036-8075 Impact factor: 47.728