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Characterization of the cytotoxic activity of the indoloquinoline alkaloid cryptolepine in human tumour cell lines and primary cultures of tumour cells from patients.
- Source :
-
Investigational new drugs [Invest New Drugs] 2009 Oct; Vol. 27 (5), pp. 402-11. Date of Electronic Publication: 2008 Oct 14. - Publication Year :
- 2009
-
Abstract
- The plant derived indoloquinoline alkaloid cryptolepine was investigated for its cytotoxic properties in 12 human tumour cell lines and in primary cultures of tumour cells from patients. The fluorometric microculture cytotoxicity assay was used to assess cytotoxicity and DNA micro-array analysis to evaluate gene expression. Cryptolepine mean IC(50) in the cell line panel was 0.9 microM compared with 1.0 and 2.8 microM in haematological and solid tumour malignancies, respectively. Among patient solid tumour samples, those from breast cancer were the most sensitive and essentially as sensitive as haematological malignancies. Cryptolepine activity showed highest correlations to topoisomerase II and microtubule targeting drugs. In the cell lines cryptolepine activity was essentially unaffected by established mechanisms of drug resistance. A number of genes were identified as associated with cryptolepine activity. In conclusion, cryptolepine shows interesting in vitro cytotoxic properties and its further evaluation as an anti-cancer drug seems warranted.
- Subjects :
- Biomarkers, Tumor genetics
Biomarkers, Tumor metabolism
Drug Resistance, Neoplasm
Drug Screening Assays, Antitumor
Gene Expression Profiling
Humans
Molecular Structure
Neoplasms metabolism
Neoplasms pathology
Oligonucleotide Array Sequence Analysis
Tumor Cells, Cultured
Antineoplastic Agents, Phytogenic pharmacology
Indole Alkaloids pharmacology
Neoplasms drug therapy
Quinolines pharmacology
Topoisomerase II Inhibitors
Subjects
Details
- Language :
- English
- ISSN :
- 1573-0646
- Volume :
- 27
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Investigational new drugs
- Publication Type :
- Academic Journal
- Accession number :
- 18853102
- Full Text :
- https://doi.org/10.1007/s10637-008-9185-5