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PMID: 15077141 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Review

Caspase activation - stepping on the gas or releasing the brakes? Lessons from humans and flies.

Oncogene ·Vol. 23 ·No. 16 ·2004-04-12 ·Pages 2774-84

Salvesen GS, Abrams JM

Abstract

The central components of the execution phase of apoptosis in worms, flies, and humans are members of the caspase protease family. Work in Drosophila and mammalian systems has revealed a web of interactions that govern the activity of these proteases, and two fundamental control points have been identified. These are zymogen activation - the process that converts a latent caspase into its active form, and inhibition of the resulting active protease. In humans, the driving force for caspase activity is activation of the zymogens, but in Drosophila, a major thrust is derepression of caspase inhibitors. In this review, we consider evidence for these two distinct events in terms of the regulation of caspase activity. This sets the scene for therapy to reinstate the normal death mechanisms that have been overcome in a cancer cell's quest for immortality.

MeSH Terms
Animals Apoptosis Caspases/physiology Cytokines/metabolism Drosophila Drosophila Proteins/physiology Enzyme Activation Humans Inhibitor of Apoptosis Proteins Neoplasms/pathology Proteins/physiology X-Linked Inhibitor of Apoptosis Protein
Chemicals
Cytokines DIAP1 protein, Drosophila Drosophila Proteins Inhibitor of Apoptosis Proteins Proteins X-Linked Inhibitor of Apoptosis Protein XIAP protein, human Caspases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Salvesen Guy S
Program in Apoptosis and Cell Death Research, The Burnham Institute, 10901 North Torrey Pines Road, La Jolla, CA 92122, USA. gsalvesen@burnham.org
Abrams John M
Article Info
Journal
Oncogene
Abbr.
Oncogene
ISSN
0950-9232
Published
2004-04-12
Pages
2774-84
Language
English
Region
England
NLM ID
8711562
Subset
IM
Grants
NIA NIH HHS · AG12466 · United States
NIA NIH HHS · AG15402 · United States
NCI NIH HHS · CA69381 · United States
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