Home LiteratureArticle Details
PMID: 17882664 Published · ppublish English Journal Article Review

Ubiquitin ligases in cancer: ushers for degradation.

Cancer investigation ·Vol. 25 ·No. 6 ·2007-09-00 ·Pages 502-13

Newton K, Vucic D

Abstract

The regulated degradation of cellular proteins by the ubiquitin-proteasome system impacts a range of vital cellular processes in both normal and cancerous cells. An ubiquitin-activating enzyme (E1), ubiquitin-conjugating enzyme (E2), and ubiquitin ligase (E3) catalyzes the conjugation of the protein ubiquitin to a target protein and, thereby, tags that protein for recognition and destruction by the proteasome. Ubiquitin ligases are particularly interesting because they determine substrate selection. This review examines the role of dysregulated ubiquitin ligase activity in the development and progression of various cancers, and highlights why ubiquitin ligases have emerged as extremely attractive targets for therapeutic intervention in a number of human malignancies.

MeSH Terms
Humans Neoplasms/drug therapy,enzymology,pathology Ubiquitin-Protein Ligases/classification,drug effects,metabolism
Chemicals
Ubiquitin-Protein Ligases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Newton Kim
Department of Physiological Chemistry, Genentech, Inc., South San Francisco, California 94110, USA.
Vucic Domagoj
Article Info
Journal
Cancer investigation
Abbr.
Cancer Invest
ISSN
0735-7907
Published
2007-09-00
Pages
502-13
Language
English
Region
England
NLM ID
8307154
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com