Abstract |
In this issue of Cancer Cell, Nickeleit et al. (2008) identify a new proteasome inhibitor, argyrin A, and show that it induces apoptosis and inhibits angiogenesis via p27-dependent mechanisms. Their observations challenge current thinking about how this class of promising cancer therapies works and why they selectively kill cancer cells.
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Authors | David J McConkey |
Journal | Cancer cell
(Cancer Cell)
Vol. 14
Issue 1
Pg. 1-2
(Jul 08 2008)
ISSN: 1878-3686 [Electronic] United States |
PMID | 18598936
(Publication Type: Comment, Journal Article)
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Chemical References |
- Angiogenesis Inhibitors
- Boronic Acids
- CDKN1B protein, human
- Cysteine Proteinase Inhibitors
- Intracellular Signaling Peptides and Proteins
- Proteasome Inhibitors
- Pyrazines
- Cyclin-Dependent Kinase Inhibitor p27
- Bortezomib
- Proteasome Endopeptidase Complex
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Topics |
- Angiogenesis Inhibitors
(pharmacology, therapeutic use)
- Animals
- Apoptosis
(drug effects)
- Blood Vessels
(drug effects, pathology)
- Boronic Acids
(pharmacology)
- Bortezomib
- Cell Cycle
(drug effects)
- Cell Proliferation
(drug effects)
- Cyclin-Dependent Kinase Inhibitor p27
- Cysteine Proteinase Inhibitors
(pharmacology, therapeutic use)
- Dose-Response Relationship, Drug
- Humans
- Intracellular Signaling Peptides and Proteins
(metabolism)
- Necrosis
- Neoplasms
(blood supply, drug therapy, enzymology, pathology)
- Neovascularization, Pathologic
(enzymology, prevention & control)
- Proteasome Endopeptidase Complex
(genetics, metabolism)
- Proteasome Inhibitors
- Protein Processing, Post-Translational
(drug effects)
- Pyrazines
(pharmacology)
- Time Factors
- Up-Regulation
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