Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2003-1-13
pubmed:abstractText
Apoptosis, a cell death programme mediated by the caspase family of cysteine proteases, is essential for appropriate removal of excess cells in many developmental and physiological settings. It would, however, be very dangerous for the organism to depend on a single protease family for clearance of unwanted and potentially dangerous cells. Indeed, the exclusive role of caspases in the execution of programmed cell death (PCD) has been challenged recently, and the understanding of the molecular control of alternative death pathways is emerging. Here, I review recently discovered triggers and molecular regulators of caspase-independent cell death programmes and discuss their potential as therapeutic targets for the treatment of cancer.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
0785-3890
pubmed:author
pubmed:issnType
Print
pubmed:volume
34
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
480-8
pubmed:dateRevised
2007-7-25
pubmed:meshHeading
pubmed:year
2002
pubmed:articleTitle
Programmed cell death: many ways for cells to die decently.
pubmed:affiliation
Apoptosis Laboratory, Institute of Cancer Biology, Danish Cancer Society, Strandhoulevarden 49, DK-2100 Copenhagen, Denmark. mhj@biobase.dk
pubmed:publicationType
Journal Article, Review, Research Support, Non-U.S. Gov't