Unknown

Dataset Information

0

Clinical significance of in vivo cytarabine-induced gene expression signature in AML.


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.

SUBMITTER: Lamba JK 

PROVIDER: S-EPMC4794368 | biostudies-literature | 2016

REPOSITORIES: biostudies-literature

altmetric image

Publications


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 tr  ...[more]

Similar Datasets

| S-EPMC7594404 | biostudies-literature
2016-07-04 | E-GEOD-52919 | biostudies-arrayexpress
2016-01-02 | GSE52919 | GEO
| S-EPMC3139433 | biostudies-literature
| S-EPMC5593973 | biostudies-literature
| S-EPMC4060157 | biostudies-literature
| S-EPMC4612499 | biostudies-other
| S-EPMC5420795 | biostudies-literature
| S-EPMC5352074 | biostudies-literature
| 2659791 | ecrin-mdr-crc