Abstract |
A survival kinase, Akt, is a downstream factor in the phosphatidylinositide-3'-kinase-dependent pathway, which mediates many biological responses including glucose uptake, protein synthesis and the regulation of proliferation and apoptosis, which is assumed to contribute to acquisition of malignant properties of human cancers. Here we find that an anti- tumor antibiotic, tetrocarcin A, directly induces apoptosis of human breast cancer cells. The apoptosis is accompanied by the activation of a proteolytic cascade of caspases including caspase-3 and -9, and concomitantly decreases phosphorylation of Akt, PDK1, and PTEN, a tumor suppressor that regulates the activity of Akt through the dephosphorylation of polyphosphoinositides. Tetrocarcin A affected neither expression of Akt, PDK1, or PTEN, nor did it affect the expression of Bcl family members including Bcl-2, Bcl-X(L), and Bax. These results suggest that tetrocarcin A could be a potent chemotherapeutic agent for human breast cancer targeting the phosphatidylinositide-3'- kinase/Akt signaling pathway.
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Authors | Hiroo Nakajima, Koichi Sakaguchi, Ikuya Fujiwara, Mitsuhiko Mizuta, Mie Tsuruga, Junji Magae, Naruhiko Mizuta |
Journal | Biochemical and biophysical research communications
(Biochem Biophys Res Commun)
Vol. 356
Issue 1
Pg. 260-5
(Apr 27 2007)
ISSN: 0006-291X [Print] United States |
PMID | 17350598
(Publication Type: Journal Article)
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Chemical References |
- Aminoglycosides
- Antibiotics, Antineoplastic
- BCL2L1 protein, human
- bcl-2-Associated X Protein
- bcl-X Protein
- tetrocarcin A
- 3-Phosphoinositide-Dependent Protein Kinases
- PDPK1 protein, human
- Protein Serine-Threonine Kinases
- Proto-Oncogene Proteins c-akt
- PTEN Phosphohydrolase
- Caspase 3
- Caspase 9
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Topics |
- 3-Phosphoinositide-Dependent Protein Kinases
- Aminoglycosides
(pharmacology)
- Antibiotics, Antineoplastic
(pharmacology)
- Apoptosis
(drug effects)
- Blotting, Western
- Breast Neoplasms
(metabolism, pathology, physiopathology)
- Caspase 3
(metabolism)
- Caspase 9
(metabolism)
- Cell Line, Tumor
- Cell Survival
(drug effects)
- Dose-Response Relationship, Drug
- Enzyme Activation
(drug effects)
- Humans
- PTEN Phosphohydrolase
(metabolism)
- Phosphatidylinositol 3-Kinases
(metabolism)
- Phosphorylation
(drug effects)
- Protein Serine-Threonine Kinases
(metabolism)
- Proto-Oncogene Proteins c-akt
(metabolism)
- Signal Transduction
(drug effects)
- bcl-2-Associated X Protein
(metabolism)
- bcl-X Protein
(metabolism)
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