Peer Reviewed

1

Document Type

Article

Publication Date

15-8-2012

Keywords

Aged, Colorectal Neoplasms, Female, Humans, Immunohistochemistry, Male, Middle Aged, Multivariate Analysis, Prognosis, Proteasome Endopeptidase Complex, Tumor Markers, Biological

Comments

This article is also available at http://onlinelibrary.wiley.com/doi/10.1002/ijc.26468/abstract

Abstract

Colorectal cancer is a leading cause of cancer-related deaths worldwide. Early diagnosis and treatment of colorectal cancer is the key to improving survival rates and as such a need exists to identify patients who may benefit from adjuvant chemotherapy. The dysregulation of the ubiquitin-proteasome system (UPS) has been implicated in oncogenesis and cancer cell survival, and proteasome inhibitors are in clinical use for a number of malignancies including multiple myeloma. In our study, we examined the protein expression of several key components of the UPS in colorectal cancer using immunohistochemistry to determine expression levels of ubiquitinylated proteins and the proteasomal subunits, 20S core and Rpt4 in a cohort of 228 patients with colon cancer. Multivariate Cox analysis revealed that neither the intensity of either ubiquitinylated proteins or the 20S core was predictive in either Stage II or III colon cancer for disease free survival or overall survival. In contrast, in Stage II patients increased Rpt4 staining was significantly associated with disease free survival (Cox proportional hazard ratio 0.605; p = 0.0217). Our data suggest that Rpt4 is an independent prognostic variable for Stage II colorectal cancer and may aid in the decision of which patients undergo adjuvant chemotherapy.

Disciplines

Physics | Physiology

Citation

McCawley N, Conlon S, Hector S, Cummins RJ, Dicker P, Johnston PG, Kay EW, McNamara DA, Prehn JHM, Concannon CG. Analyzing proteasomal subunit expression reveals Rpt4 as a prognostic marker in stage II colorectal cancer. International Journal of Cancer. 2012;131(4):E494-500,

PubMed ID

21960357

DOI Link

10.1002/ijc.26468

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