Unknown,Transcriptomics,Genomics,Proteomics

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Transcription profiling of human leukemia cells treated with mercaptopurine and/or methotrexate


ABSTRACT: To elucidate the genomics of cellular responses to cancer treatment, we analyzed the expression of over 9,600 human genes in acute lymphoblastic leukemia cells before and after in vivo treatment with methotrexate and mercaptopurine given alone or in combination. Based on changes in gene expression, we identified 124 genes that accurately discriminated among the four treatments. Discriminating genes included those involved in apoptosis, mismatch repair, cell cycle control and stress response. Only 14% of genes that changed when these medications were given as single agents also changed when they were given together. These data indicate that lymphoid leukemia cells of different molecular subtypes share common pathways of genomic response to the same treatment, that changes in gene expression are treatment-specific and that gene expression can illuminate differences in cellular response to drug combinations versus single agents.

ORGANISM(S): Homo sapiens

SUBMITTER: William Evans 

PROVIDER: E-GEOD-412 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Publications

Treatment-specific changes in gene expression discriminate in vivo drug response in human leukemia cells.

Cheok Meyling H MH   Yang Wenjian W   Pui Ching-Hon CH   Downing James R JR   Cheng Cheng C   Naeve Clayton W CW   Relling Mary V MV   Evans William E WE  

Nature genetics 20030501 1


To elucidate the genomics of cellular responses to cancer treatment, we analyzed the expression of over 9,600 human genes in acute lymphoblastic leukemia cells before and after in vivo treatment with methotrexate and mercaptopurine given alone or in combination. Based on changes in gene expression, we identified 124 genes that accurately discriminated among the four treatments. Discriminating genes included those involved in apoptosis, mismatch repair, cell cycle control and stress response. Onl  ...[more]

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