| Literature DB >> 22094254 |
Liang Li1, Min Li, Canlan Sun, Liton Francisco, Sujata Chakraborty, Melanie Sabado, Tinisha McDonald, Janelle Gyorffy, Karen Chang, Shirong Wang, Wenhong Fan, Jiangning Li, Lue Ping Zhao, Jerald Radich, Stephen Forman, Smita Bhatia, Ravi Bhatia.
Abstract
Therapy-related myelodysplasia or acute myeloid leukemia (t-MDS/AML) is a major complication of cancer treatment. We compared gene expression in CD34+ cells from patients who developed t-MDS/AML after autologous hematopoietic cell transplantation (aHCT) for lymphoma with controls who did not develop t-MDS/AML. We observed altered gene expression related to mitochondrial function, metabolism, and hematopoietic regulation in pre-aHCT samples from patients who subsequently developed t-MDS/AML. Progression to overt t-MDS/AML was associated with additional alterations in cell-cycle regulatory genes. An optimal 38-gene PBSC classifier accurately distinguished patients who did or did not develop t-MDS/AML in an independent group of patients. We conclude that genetic programs associated with t-MDS/AML are perturbed long before disease onset, and accurately identify patients at risk for this complication. 2011 Elsevier Inc. All rights reserved.Entities:
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Year: 2011 PMID: 22094254 PMCID: PMC3220884 DOI: 10.1016/j.ccr.2011.09.011
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743