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Metabolomics,Unknown,Transcriptomics,Genomics,Proteomics

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Early and late TKI response of CML stem cells

ABSTRACT: Chronic myeloid leukaemia (CML) is a clonal haemopoietic stem cell (HSC) disorder associated with the BCR-ABL oncogene, which encodes a constitutively active tyrosine kinase. We have demonstrated the existence of CML HSC which are resistant to the tyrosine kinase inhibitors (TKI). We have hypothesised that CML stem cells are dependent on key survival pathways that are induced by TKI treatment. In order to elucidate these key survival pathways, we have investigated the transcriptional differences between CML stem/progenitor cells (CD34+38-) treated with TKIs (imatinib, dasatinib and nilotinib) at different time points (8 hours and 7 days, in the absence of growth factors) and by carrying out RNA profiling for the different populations. CD34+38- cells were isolated from chronic phase patient samples. >100ng of total RNA was amplified prior to analysis that was carried out with Affymetrix Human Gene 1.0 ST array.

ORGANISM(S): Homo sapiens

SUBMITTER: Tessa Holyoake

PROVIDER: E-MTAB-2594 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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