SPOP Promotes Ubiquitination and Degradation of the ERG Oncoprotein to Suppress Prostate Cancer Progression.

Journal Article (Journal Article)

The ERG gene is fused to TMPRSS2 in approximately 50% of prostate cancers (PrCa), resulting in its overexpression. However, whether this is the sole mechanism underlying ERG elevation in PrCa is currently unclear. Here we report that ERG ubiquitination and degradation are governed by the Cullin 3-based ubiquitin ligase SPOP and that deficiency in this pathway leads to aberrant elevation of the ERG oncoprotein. Specifically, we find that truncated ERG (ΔERG), encoded by the ERG fusion gene, is stabilized by evading SPOP-mediated destruction, whereas prostate cancer-associated SPOP mutants are also deficient in promoting ERG ubiquitination. Furthermore, we show that the SPOP/ERG interaction is modulated by CKI-mediated phosphorylation. Importantly, we demonstrate that DNA damage drugs, topoisomerase inhibitors, can trigger CKI activation to restore the SPOP/ΔERG interaction and its consequent degradation. Therefore, SPOP functions as a tumor suppressor to negatively regulate the stability of the ERG oncoprotein in prostate cancer.

Full Text

Duke Authors

Cited Authors

  • Gan, W; Dai, X; Lunardi, A; Li, Z; Inuzuka, H; Liu, P; Varmeh, S; Zhang, J; Cheng, L; Sun, Y; Asara, JM; Beck, AH; Huang, J; Pandolfi, PP; Wei, W

Published Date

  • September 17, 2015

Published In

Volume / Issue

  • 59 / 6

Start / End Page

  • 917 - 930

PubMed ID

  • 26344095

Pubmed Central ID

  • PMC4575912

Electronic International Standard Serial Number (EISSN)

  • 1097-4164

Digital Object Identifier (DOI)

  • 10.1016/j.molcel.2015.07.026


  • eng

Conference Location

  • United States