Home LiteratureArticle Details
PMID: 9695821 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S. Review

The caspase-RB connection in cell death.

Trends in cell biology ·Vol. 8 ·No. 3 ·1998-03-00 ·Pages 116-20

Tan X, Wang JY

Abstract

Execution of the cell-death programme requires the activation of a family of cysteine proteases known as caspases. Specific cellular proteins are cleaved by caspases during apoptosis, including the retinoblastoma tumour-suppressor protein (RB1). A caspase-resistant RB1 can attenuate the death response to tumour necrosis factor alpha. The cleavage of RB1 during cell death, together with the increased cell death during embryonic development of Rb-knockout mice, suggests that RB1 degradation contributes to the activation of the cell-death pathway.

MeSH Terms
Animals Cell Death/physiology Cysteine Endopeptidases/metabolism,physiology Cytoskeletal Proteins/metabolism,physiology Humans Retinoblastoma Protein/metabolism,physiology
Chemicals
Cytoskeletal Proteins Retinoblastoma Protein Cysteine Endopeptidases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Tan X
Dept of Biology, University of California, San Diego, La Jolla 92093-0322, USA.
Wang J Y
Article Info
Journal
Trends in cell biology
Abbr.
Trends Cell Biol
ISSN
0962-8924
Published
1998-03-00
Pages
116-20
Language
English
Region
England
NLM ID
9200566
Subset
IM
Grants
NCI NIH HHS · R01 CA058320 · United States
NCI NIH HHS · CA 58320 · United States
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