Targeting ubiquitination for cancer therapies

Author:

Morrow John Kenneth12,Lin Hui-Kuan3,Sun Shao-Cong4,Zhang Shuxing1

Affiliation:

1. Integrated Molecular Discovery Laboratory, Department of Experimental Therapeutics, MD Anderson Cancer Center, Houston, TX 77030, USA

2. The University of Texas Graduate School of Biomedical Sciences, Houston, TX 77030, USA

3. Department of Molecular & Cellular Oncology, MD Anderson Cancer Center, Houston, TX 77030, USA

4. Department of Immunology, MD Anderson Cancer Center, Houston, TX 77030, USA

Abstract

Ubiquitination, the structured degradation and turnover of cellular proteins, is regulated by the ubiquitin–proteasome system (UPS). Most proteins that are critical for cellular regulations and functions are targets of the process. Ubiquitination is comprised of a sequence of three enzymatic steps, and aberrations in the pathway can lead to tumor development and progression as observed in many cancer types. Recent evidence indicates that targeting the UPS is effective for certain cancer treatment, but many more potential targets might have been previously overlooked. In this review, we will discuss the current state of small molecules that target various elements of ubiquitination. Special attention will be given to novel inhibitors of E3 ubiquitin ligases, especially those in the SCF family.

Publisher

Future Science Ltd

Subject

Drug Discovery,Pharmacology,Molecular Medicine

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