| Literature DB >> 20082857 |
Min Jin Kim1, Hoi Soo Yoon, Gayoung Lim, So Young Kim, Hee Joo Lee, Jin-Tae Suh, Juhie Lee, Woo-In Lee, Tae Sung Park.
Abstract
Entire ABL1 gene deletion without BCR/ABL1 rearrangement is a rare phenomenon, with only four cases previously reported. Here we describe a fifth case of ABL1 deletion without BCR/ABL1 rearrangement in an adolescent patient with precursor B-cell lymphoblastic leukemia (B-ALL) and review the relevant literature. It is not clear how ABL1 deletion affects leukemogenesis; however, it is plausible that ABL1 deletion without BCR/ABL1 rearrangement is a rare but recurrent genetic abnormality in precursor B-ALL patients. Further studies are needed to evaluate the extent of the submicroscopic defects in chromosome 9 including ABL1 gene deletion, as well as treatment response and prognosis in long-term follow-up of such patients. Copyright 2010 Elsevier Inc. All rights reserved.Entities:
Mesh:
Substances:
Year: 2010 PMID: 20082857 DOI: 10.1016/j.cancergencyto.2009.09.018
Source DB: PubMed Journal: Cancer Genet Cytogenet ISSN: 0165-4608