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Nature DOI:10.1038/nature12688

A melanocyte lineage program confers resistance to MAP kinase pathway inhibition.

Publication TypeJournal Article
Year of Publication2013
AuthorsJohannessen, CM, Johnson, LA, Piccioni, F, Townes, A, Frederick, DT, Donahue, MK, Narayan, R, Flaherty, KT, Wargo, JA, Root, DE, Garraway, LA
JournalNature
Volume504
Issue7478
Pages138-42
Date Published2013 Dec 05
ISSN1476-4687
KeywordsAntineoplastic Agents, Cell Line, Tumor, Cell Lineage, CREB-Binding Protein, Cyclic AMP, Drug Resistance, Neoplasm, Gene Expression Regulation, Neoplastic, HEK293 Cells, Humans, Melanocytes, Melanoma, Mitogen-Activated Protein Kinases, Protein Kinase Inhibitors, Signal Transduction, Transcription Factors
Abstract

Malignant melanomas harbouring point mutations (Val600Glu) in the serine/threonine-protein kinase BRAF (BRAF(V600E)) depend on RAF-MEK-ERK signalling for tumour cell growth. RAF and MEK inhibitors show remarkable clinical efficacy in BRAF(V600E) melanoma; however, resistance to these agents remains a formidable challenge. Global characterization of resistance mechanisms may inform the development of more effective therapeutic combinations. Here we carried out systematic gain-of-function resistance studies by expressing more than 15,500 genes individually in a BRAF(V600E) melanoma cell line treated with RAF, MEK, ERK or combined RAF-MEK inhibitors. These studies revealed a cyclic-AMP-dependent melanocytic signalling network not previously associated with drug resistance, including G-protein-coupled receptors, adenyl cyclase, protein kinase A and cAMP response element binding protein (CREB). Preliminary analysis of biopsies from BRAF(V600E) melanoma patients revealed that phosphorylated (active) CREB was suppressed by RAF-MEK inhibition but restored in relapsing tumours. Expression of transcription factors activated downstream of MAP kinase and cAMP pathways also conferred resistance, including c-FOS, NR4A1, NR4A2 and MITF. Combined treatment with MAPK-pathway and histone-deacetylase inhibitors suppressed MITF expression and cAMP-mediated resistance. Collectively, these data suggest that oncogenic dysregulation of a melanocyte lineage dependency can cause resistance to RAF-MEK-ERK inhibition, which may be overcome by combining signalling- and chromatin-directed therapeutics.

URLhttp://dx.doi.org/10.1038/nature12688
DOI10.1038/nature12688
Pubmed

http://www.ncbi.nlm.nih.gov/pubmed/24185007?dopt=Abstract

Alternate JournalNature
PubMed ID24185007
PubMed Central IDPMC4098832
Grant ListP01 CA163222 / CA / NCI NIH HHS / United States
P50 CA093683 / CA / NCI NIH HHS / United States
U54 HG006093 / HG / NHGRI NIH HHS / United States
DP2OD002750 / OD / NIH HHS / United States
DP2 OD002750 / OD / NIH HHS / United States
P50CA93683 / CA / NCI NIH HHS / United States
R33 CA155554 / CA / NCI NIH HHS / United States
U54 CA112962 / CA / NCI NIH HHS / United States
U01 HG006492 / HG / NHGRI NIH HHS / United States