Abstract |
The effect of N-1-(3,5-dimethyladamantyl)maleimide (DMAMI) on the growth of Colo205 human colon cancer cells was examined both in vitro and in vivo. Flow cytometry analysis showed a decrease of G2/M Colo205 cells at 4-6 h after treatment with DMAMI prior to accumulation of apoptotic cells at 24 h. Significant changes in cell morphology, i.e. shrinkage and chromatin condensation of cells, were observed after treatment with DMAMI. In the analysis of the apoptosis markers, it was found that the increase of Annexin V binding to membrane, peroxide radicals, dissipation of the mitochondrial membrane potential, and the activation of caspase-3, -8 and -9 were all evident at 4-6 h after treatment with DMAMI. In vivo analysis showed that treatment of Colo205 tumor-bearing SCID mice with DMAMI (230 mg/kg, intratumoral, once) resulted in rapid tumor damage that leads to significant tumor growth inhibition and no obvious acute toxicity. These results suggest that DMAMI has potential for local treatment of cancer.
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Authors | Jane-Jen Wang, Yaw-Terng Chern, Yuh-Fang Chang, Tsung-Yun Liu, Chin-Wen Chi |
Journal | Anti-cancer drugs
(Anticancer Drugs)
Vol. 13
Issue 5
Pg. 533-43
(Jun 2002)
ISSN: 0959-4973 [Print] England |
PMID | 12045465
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Annexin A5
- Antineoplastic Agents
- Cytochrome c Group
- Free Radicals
- Maleimides
- N-1-(3,5-dimethyladamantyl)maleimide
- Caspases
- Adamantane
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Topics |
- Adamantane
(analogs & derivatives, pharmacology)
- Animals
- Annexin A5
(metabolism)
- Antineoplastic Agents
(pharmacology)
- Apoptosis
(drug effects)
- Caspases
(metabolism)
- Cell Division
(drug effects)
- Colonic Neoplasms
(metabolism, pathology)
- Cytochrome c Group
(metabolism)
- Dose-Response Relationship, Drug
- Flow Cytometry
- Free Radicals
(metabolism)
- G2 Phase
(drug effects)
- Humans
- Maleimides
(pharmacology)
- Membrane Potentials
(drug effects)
- Mice
- Mice, SCID
- Mitochondria
(drug effects, metabolism)
- Mitosis
(drug effects)
- Necrosis
- Tumor Cells, Cultured
(drug effects, metabolism)
- Xenograft Model Antitumor Assays
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