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Metabolomics,Unknown,Transcriptomics,Genomics,Proteomics

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Response and resistance to BET bromodomain inhibitors in triple negative breast cancer

ABSTRACT: This SuperSeries is composed of the SubSeries listed below. Refer to individual Series

ORGANISM(S): Homo sapiens

SUBMITTER: Kornelia Polyak

PROVIDER: E-GEOD-63584 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Response and resistance to BET bromodomain inhibitors in triple-negative breast cancer.

Shu Shaokun S Lin Charles Y CY He Housheng Hansen HH Witwicki Robert M RM Tabassum Doris P DP Roberts Justin M JM Janiszewska Michalina M Huh Sung Jin SJ Liang Yi Y Ryan Jeremy J Doherty Ernest E Mohammed Hisham H Guo Hao H Stover Daniel G DG Ekram Muhammad B MB Brown Jonathan J D'Santos Clive C Krop Ian E IE Dillon Deborah D McKeown Michael M Ott Christopher C Qi Jun J Ni Min M Rao Prakash K PK Duarte Melissa M Wu Shwu-Yuan SY Chiang Cheng-Ming CM Anders Lars L Young Richard A RA Winer Eric E Letai Antony A Barry William T WT Carroll Jason S JS Long Henry H Brown Myles M Liu X Shirley XS Meyer Clifford A CA Bradner James E JE Polyak Kornelia K

Nature 20160106 7586

Triple-negative breast cancer (TNBC) is a heterogeneous and clinically aggressive disease for which there is no targeted therapy. BET bromodomain inhibitors, which have shown efficacy in several models of cancer, have not been evaluated in TNBC. These inhibitors displace BET bromodomain proteins such as BRD4 from chromatin by competing with their acetyl-lysine recognition modules, leading to inhibition of oncogenic transcriptional programs. Here we report the preferential sensitivity of TNBCs to ...[more]

PMID: 26735014

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