| Literature DB >> 25270907 |
Roberta La Starza1, Chiara Borga2, Gianluca Barba1, Valentina Pierini1, Claire Schwab3, Caterina Matteucci1, Anair G Lema Fernandez1, Anna Leszl2, Gianni Cazzaniga4, Sabina Chiaretti5, Giuseppe Basso2, Christine J Harrison3, Geertruy Te Kronnie2, Cristina Mecucci1.
Abstract
MYC translocations represent a genetic subtype of T-lineage acute lymphoblastic leukemia (T-ALL), which occurs at an incidence of ∼6%, assessed within a cohort of 196 T-ALL patients (64 adults and 132 children). The translocations were of 2 types; those rearranged with the T-cell receptor loci and those with other partners. MYC translocations were significantly associated with the TAL/LMO subtype of T-ALL (P = .018) and trisomies 6 (P < .001) and 7 (P < .001). Within the TAL/LMO subtype, gene expression profiling identified 148 differentially expressed genes between patients with and without MYC translocations; specifically, 77 were upregulated and 71 downregulated in those with MYC translocations. The poor prognostic marker, CD44, was among the upregulated genes. MYC translocations occurred as secondary abnormalities, present in subclones in one-half of the cases. Longitudinal studies indicated an association with induction failure and relapse.Entities:
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Year: 2014 PMID: 25270907 DOI: 10.1182/blood-2014-06-578856
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113