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- W2001515311 endingPage "648" @default.
- W2001515311 startingPage "633" @default.
- W2001515311 abstract "Cell death inhibition is a very successful strategy that cancer cells employ to combat the immune system and various anticancer therapies. Inhibitor of apoptosis (IAP) proteins possess a wide range of biological activities that promote cancer survival and proliferation. One of them, X-chromosome-linked IAP is a direct inhibitor of proapoptotic executioners, caspases. Cellular IAP proteins regulate expression of antiapoptotic molecules and prevent assembly of proapoptotic protein signaling complexes, while survivin regulates cell division. In addition, amplifications, mutations and chromosomal translocations of IAP genes are associated with various malignancies. Several therapeutic strategies have been designed to target IAP proteins, including a small-molecule approach that is based on mimicking the IAP-binding motif of an endogenous IAP antagonist – the second mitochondrial activator of caspases. Other strategies involve antisense nucleotides and transcriptional repression. The main focus of this article is to provide an update on IAP protein biology and perspectives on the development of IAP-targeting therapeutics." @default.
- W2001515311 created "2016-06-24" @default.
- W2001515311 creator A5048067233 @default.
- W2001515311 creator A5052364035 @default.
- W2001515311 date "2011-05-01" @default.
- W2001515311 modified "2023-10-18" @default.
- W2001515311 title "Inhibitor of apoptosis proteins: fascinating biology leads to attractive tumor therapeutic targets" @default.
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