Oncogenic function of SCCRO5/DCUN1D5 requires its Neddylation E3 activity and nuclear localization.

Clin Cancer Res

Authors' Affiliations: Department of Surgery, Laboratory of Epithelial Cancer Biology and Departments of Epidemiology and Biostatistics and Pathology, Memorial Sloan-Kettering Cancer Center, New York, New York.

Published: January 2014

AI Article Synopsis

  • The study investigates how SCCRO5 (DCUN1D5) contributes to cancer development by analyzing its expression in various cancer samples.
  • Findings show that high levels of SCCRO5 are linked to poorer survival rates in patients with oral and lung cancers, indicating its role in promoting cancer cell viability.
  • The research concludes that SCCRO5 functions as part of a neddylation E3 complex, which plays a crucial role in its oncogenic effects, highlighting the importance of both its neddylation activity and nuclear localization for its function in cancer.

Article Abstract

Purpose: To determine mechanisms by which SCCRO5 (aka DCUN1D5) promotes oncogenesis.

Experimental Design: SCCRO5 mRNA and protein expression were assessed in 203 randomly selected primary cancer tissue samples, matched histologically normal tissues, and cell lines by use of real-time PCR and Western blot analysis. SCCRO5 overexpression was correlated with survival. The effect of SCCRO5 knockdown on viability was assessed in selected cancer cell lines. Structure-function studies were performed to determine the SCCRO5 residues required for binding to the neddylation components, for neddylation-promoting activity, and for transformation.

Results: In oral and lung squamous cell carcinomas, SCCRO5 mRNA levels corresponded with protein levels and overexpression correlated with decreased disease-specific survival. Knockdown of SCCRO5 by RNAi resulted in a selective decrease in the viability of cancer cells with high endogenous levels, suggesting the presence of oncogene addiction. SCCRO5 promoted cullin neddylation while maintaining conserved reaction processivity paradigms involved in ubiquitin and ubiquitin-like protein conjugation, establishing it as a component of the neddylation E3. Neddylation activities in vitro required the potentiating of neddylation (PONY) domain but not the nuclear localization sequence (NLS) domain. In contrast, both the NLS domain and the PONY domain were required for transformation of NIH-3T3 cells.

Conclusions: Our data suggest that SCCRO5 has oncogenic potential that requires its function as a component of the neddylation E3. Neddylation activity and nuclear localization of SCCRO5 are important for its in vivo function.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4191716PMC
http://dx.doi.org/10.1158/1078-0432.CCR-13-1252DOI Listing

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