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Nature DOI:10.1038/nature18003

Proteogenomics connects somatic mutations to signalling in breast cancer.

Publication TypeJournal Article
Year of Publication2016
AuthorsMertins, P, Mani, DR, Ruggles, KV, Gillette, MA, Clauser, KR, Wang, P, Wang, X, Qiao, JW, Cao, S, Petralia, F, Kawaler, E, Mundt, F, Krug, K, Tu, Z, Lei, JT, Gatza, ML, Wilkerson, M, Perou, CM, Yellapantula, V, Huang, KL, Lin, C, McLellan, MD, Yan, P, Davies, SR, Townsend, RR, Skates, SJ, Wang, J, Zhang, B, Kinsinger, CR, Mesri, M, Rodriguez, H, Ding, L, Paulovich, AG, Fenyö, D, Ellis, MJ, Carr, SA, NCI, CPTAC
JournalNature
Volume534
Issue7605
Pages55-62
Date Published2016/05/25
ISSN0028-0836
Abstract

Somatic mutations have been extensively characterized in breast cancer, but the effects of these genetic alterations on the proteomic landscape remain poorly understood. Here we describe quantitative mass-spectrometry-based proteomic and phosphoproteomic analyses of 105 genomically annotated breast cancers, of which 77 provided high-quality data. Integrated analyses provided insights into the somatic cancer genome including the consequences of chromosomal loss, such as the 5q deletion characteristic of basal-like breast cancer. Interrogation of the 5q trans-effects against the Library of Integrated Network-based Cellular Signatures, connected loss of CETN3 and SKP1 to elevated expression of epidermal growth factor receptor (EGFR), and SKP1 loss also to increased SRC tyrosine kinase. Global proteomic data confirmed a stromal-enriched group of proteins in addition to basal and luminal clusters, and pathway analysis of the phosphoproteome identified a G-protein-coupled receptor cluster that was not readily identified at the mRNA level. In addition to ERBB2, other amplicon-associated highly phosphorylated kinases were identified, including CDK12, PAK1, PTK2, RIPK2 and TLK2. We demonstrate that proteogenomic analysis of breast cancer elucidates the functional consequences of somatic mutations, narrows candidate nominations for driver genes within large deletions and amplified regions, and identifies therapeutic targets.

URLhttp://dx.doi.org/10.1038/nature18003
DOI10.1038/nature18003
Pubmed

http://www.ncbi.nlm.nih.gov/pubmed/27251275?dopt=Abstract

PubMed ID27251275
PubMed Central IDPMC5102256