Role of Ubiquitin Ligases and the Proteasome in Oncogenesis: Novel Targets for Anticancer Therapies

Author:

Micel Lindsey N.1,Tentler John J.1,Smith Peter G.1,Eckhardt Gail S.1

Affiliation:

1. Lindsey N. Micel, John J. Tentler, and S. Gail Eckhardt, University of Colorado School of Medicine, Aurora; Lindsey N. Micel, Children's Hospital Colorado, Aurora, CO; and Peter G. Smith, H3 Biomedicine, Cambridge, MA.

Abstract

The ubiquitin proteasome system (UPS) regulates the ubiquitination, and thus degradation and turnover, of many proteins vital to cellular regulation and function. The UPS comprises a sequential series of enzymatic processes using four key enzyme families: E1 (ubiquitin-activating enzymes), E2 (ubiquitin-carrier proteins), E3 (ubiquitin-protein ligases), and E4 (ubiquitin chain assembly factors). Because the UPS is a crucial regulator of the cell cycle, and abnormal cell-cycle control can lead to oncogenesis, aberrancies within the UPS pathway can result in a malignant cellular phenotype and thus has become an attractive target for novel anticancer agents. This article will provide an overall review of the mechanics of the UPS, describe aberrancies leading to cancer, and give an overview of current drug therapies selectively targeting the UPS.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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