| Literature DB >> 26366682 |
Jatinder K Lamba1, Stanley Pounds2, Xueyuan Cao2, Kristine R Crews3, Christopher R Cogle4, Neha Bhise1, Susana C Raimondi5, James R Downing5, Sharyn D Baker3, Raul C Ribeiro6, Jeffrey E Rubnitz6.
Abstract
Despite initial remission, ∼60-70% of adult and 30% of pediatric patients experience relapse or refractory AML. Studies so far have identified base line gene expression profiles of pathogenic and prognostic significance in AML; however, the extent of change in gene expression post-initiation of treatment has not been investigated. Exposure of leukemic cells to chemotherapeutic agents such as cytarabine, a mainstay of AML chemotherapy, can trigger adaptive response by influencing leukemic cell transcriptome and, hence, development of resistance or refractory disease. It is, however, challenging to perform such a study due to lack of availability of specimens post-drug treatment. The primary objective of this study was to identify in vivo cytarabine-induced changes in leukemia cell transcriptome and to evaluate their impact on clinical outcome. The results highlight genes relevant to cytarabine resistance and support the concept of targeting cytarabine-induced genes as a means of improving response.Entities:
Keywords: Cytarabine; acute myeloid leukemia; event-free survival; gene expression
Mesh:
Substances:
Year: 2015 PMID: 26366682 PMCID: PMC4794368 DOI: 10.3109/10428194.2015.1086918
Source DB: PubMed Journal: Leuk Lymphoma ISSN: 1026-8022