Abstract |
The inhibitor of apoptosis protein (IAP) family encodes a group of Baculovirus IAP repeat domain (BIR)-containing proteins that suppress apoptosis. Some of the IAPs, survivin and XIAP in particular, are differentially overexpressed in many types of human cancer and are deemed attractive anticancer targets. Here we review the regulation of survivin expression and survivin's functions in both normal and cancerous cells, and some of the current survivin-targeted cancer therapy. We further discuss the possible mechanisms of tetra-O-methyl nordihydroguaretic acid (M(4)N), a global transcription inhibitor, in the induction of cancer cell death in tumors via survivin-dependent and -independent pathways.
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Authors | Ru Chih C Huang, Chih Chuan Chang, David Mold |
Journal | Seminars in oncology
(Semin Oncol)
Vol. 33
Issue 4
Pg. 479-85
(Aug 2006)
ISSN: 0093-7754 [Print] United States |
PMID | 16890802
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't, Review)
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Chemical References |
- BIRC5 protein, human
- Inhibitor of Apoptosis Proteins
- Microtubule-Associated Proteins
- Neoplasm Proteins
- Survivin
- terameprocol
- Masoprocol
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Topics |
- Apoptosis
(drug effects, physiology)
- Cell Division
(physiology)
- Humans
- Inhibitor of Apoptosis Proteins
- Masoprocol
(analogs & derivatives, chemistry, pharmacology)
- Microtubule-Associated Proteins
(antagonists & inhibitors, genetics, metabolism)
- Necrosis
- Neoplasm Proteins
(antagonists & inhibitors, genetics, metabolism)
- Neoplasms
(pathology)
- Survivin
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