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PMID: 12120092 Published · ppublish English Journal Article Review

Apoptosis-based therapies.

Nature reviews. Drug discovery ·Vol. 1 ·No. 2 ·2002-02-00 ·Pages 111-21

Reed JC

Abstract

Many of today's medical illnesses can be attributed directly or indirectly to problems with apoptosis--a programmed cell-suicide mechanism. Disorders in which defective regulation of apoptosis contributes to disease pathogenesis or progression can involve either cell accumulation, in which cell eradication or cell turnover is impaired, or cell loss, in which the cell-suicide programme is inappropriately triggered. Identification of the genes and gene products that are responsible for apoptosis, together with emerging information about the mechanisms of action and structures of apoptotic regulatory and effector proteins, has laid a foundation for the discovery of drugs, some of which are now undergoing evaluation in human clinical trials.

MeSH Terms
Animals Apoptosis/drug effects Apoptotic Protease-Activating Factor 1 Caspase Inhibitors Genes, bcl-2 Genes, p53 Genetic Therapy Humans Inhibitor of Apoptosis Proteins Insect Proteins/antagonists & inhibitors,genetics Neoplasms/therapy Proteins/antagonists & inhibitors Transcription Factors/physiology
Chemicals
APAF1 protein, human Apoptotic Protease-Activating Factor 1 Caspase Inhibitors Inhibitor of Apoptosis Proteins Insect Proteins Proteins Transcription Factors
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Reed John C
Burnham Institute, 10901 North Torrey Pines Road, La Jolla, California 92037, USA. jreed@burnham.org
Article Info
Journal
Nature reviews. Drug discovery
Abbr.
Nat Rev Drug Discov
ISSN
1474-1776
Published
2002-02-00
Pages
111-21
Language
English
Region
England
NLM ID
101124171
Subset
IM
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