The long tail of oncogenic drivers in prostate cancer. Academic Article uri icon

Overview

abstract

  • Comprehensive genomic characterization of prostate cancer has identified recurrent alterations in genes involved in androgen signaling, DNA repair, and PI3K signaling, among others. However, larger and uniform genomic analysis may identify additional recurrently mutated genes at lower frequencies. Here we aggregate and uniformly analyze exome sequencing data from 1,013 prostate cancers. We identify and validate a new class of E26 transformation-specific (ETS)-fusion-negative tumors defined by mutations in epigenetic regulators, as well as alterations in pathways not previously implicated in prostate cancer, such as the spliceosome pathway. We find that the incidence of significantly mutated genes (SMGs) follows a long-tail distribution, with many genes mutated in less than 3% of cases. We identify a total of 97 SMGs, including 70 not previously implicated in prostate cancer, such as the ubiquitin ligase CUL3 and the transcription factor SPEN. Finally, comparing primary and metastatic prostate cancer identifies a set of genomic markers that may inform risk stratification.

authors

publication date

  • April 2, 2018

Research

keywords

  • Oncogenes
  • Prostatic Neoplasms

Identity

PubMed Central ID

  • PMC6107367

Scopus Document Identifier

  • 85044725681

Digital Object Identifier (DOI)

  • 10.1038/s41588-018-0078-z

PubMed ID

  • 29610475

Additional Document Info

volume

  • 50

issue

  • 5