SPOP mutation leads to genomic instability in prostate cancer

نویسندگان

  • Gunther Boysen
  • Christopher E Barbieri
  • Davide Prandi
  • Mirjam Blattner
  • Sung-Suk Chae
  • Arun Dahija
  • Srilakshmi Nataraj
  • Dennis Huang
  • Clarisse Marotz
  • Limei Xu
  • Julie Huang
  • Paola Lecca
  • Sagar Chhangawala
  • Deli Liu
  • Pengbo Zhou
  • Andrea Sboner
  • Johann S de Bono
  • Francesca Demichelis
  • Yariv Houvras
  • Mark A Rubin
  • Joaquín M Espinosa
چکیده

Genomic instability is a fundamental feature of human cancer often resulting from impaired genome maintenance. In prostate cancer, structural genomic rearrangements are a common mechanism driving tumorigenesis. However, somatic alterations predisposing to chromosomal rearrangements in prostate cancer remain largely undefined. Here, we show that SPOP, the most commonly mutated gene in primary prostate cancer modulates DNA double strand break (DSB) repair, and that SPOP mutation is associated with genomic instability. In vivo, SPOP mutation results in a transcriptional response consistent with BRCA1 inactivation resulting in impaired homology-directed repair (HDR) of DSB. Furthermore, we found that SPOP mutation sensitizes to DNA damaging therapeutic agents such as PARP inhibitors. These results implicate SPOP as a novel participant in DSB repair, suggest that SPOP mutation drives prostate tumorigenesis in part through genomic instability, and indicate that mutant SPOP may increase response to DNA-damaging therapeutics.

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عنوان ژورنال:

دوره 4  شماره 

صفحات  -

تاریخ انتشار 2015