LA-12 overcomes confluence-dependent resistance of HT-29 colon cancer cells to Pt (II) compounds
Language English Country Greece Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
20530425
PII: 30/4/1183
Knihovny.cz E-resources
- MeSH
- Adenocarcinoma drug therapy MeSH
- Amantadine analogs & derivatives pharmacology MeSH
- Apoptosis drug effects MeSH
- Cell Adhesion drug effects MeSH
- HT29 Cells MeSH
- Drug Resistance, Neoplasm MeSH
- Cisplatin pharmacology MeSH
- Humans MeSH
- Colonic Neoplasms drug therapy pathology MeSH
- Organoplatinum Compounds pharmacology MeSH
- Oxaliplatin MeSH
- Antineoplastic Agents pharmacology MeSH
- Dose-Response Relationship, Drug MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Amantadine MeSH
- bis(acetato)(1-adamantylamine)amminedichloroplatinum(IV) MeSH Browser
- Cisplatin MeSH
- Organoplatinum Compounds MeSH
- Oxaliplatin MeSH
- Antineoplastic Agents MeSH
BACKGROUND: LA-12 is a new platinum (IV) drug with promising cytotoxic effects in a wide range of cancer cell lines. Its confluence-dependent effects were compared with cisplatin (CDDP) and oxaliplatin (L-OHP) in HT-29 cells. MATERIALS AND METHODS: Cytotoxicity was determined by MTT test, eosin exclusion assay, and cell number quantification. The cell cycle was analysed using propidium iodide DNA staining (flow cytometry), apoptosis by phosphatidylserine externalisation (annexin-V assay), mitochondrial membrane potential by flow cytometry, nuclear morphology by means of fluorescence microscopy, and PARP cleavage by Western blotting. RESULTS: While L-OHP and CDDP were practically inactive in the subconfluent cell population, LA-12 showed a similar toxicity in both subconfluent and growing populations. All compounds induced apoptosis, although with different potentials. CONCLUSION: LA-12 was able to overcome confluence-dependent resistance of HT-29 cells observed for other platinum compounds, which may have potential therapeutic use in slowly growing tumours.