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Anticancer alkaloid lamellarins inhibit protein kinases.
- Source :
-
Marine drugs [Mar Drugs] 2008; Vol. 6 (4), pp. 514-27. Date of Electronic Publication: 2008 Oct 07. - Publication Year :
- 2008
-
Abstract
- Lamellarins, a family of hexacyclic pyrrole alkaloids originally isolated from marine invertebrates, display promising anti-tumor activity. They induce apoptotic cell death through multi-target mechanisms, including inhibition of topoisomerase I, interaction with DNA and direct effects on mitochondria. We here report that lamellarins inhibit several protein kinases relevant to cancer such as cyclin-dependent kinases, dual-specificity tyrosine phosphorylation activated kinase 1A, casein kinase 1, glycogen synthase kinase-3 and PIM-1. A good correlation is observed between the effects of lamellarins on protein kinases and their action on cell death, suggesting that inhibition of specific kinases may contribute to the cytotoxicity of lamellarins. Structure/activity relationship suggests several paths for the optimization of lamellarins as kinase inhibitors.
- Subjects :
- Alkaloids chemistry
Alkaloids isolation & purification
Animals
Antineoplastic Agents chemistry
Antineoplastic Agents isolation & purification
Antineoplastic Agents pharmacology
Cell Death drug effects
Heterocyclic Compounds, 4 or More Rings chemistry
Heterocyclic Compounds, 4 or More Rings isolation & purification
Humans
Neoplasms physiopathology
Protein Kinase Inhibitors chemistry
Protein Kinase Inhibitors isolation & purification
Protein Kinase Inhibitors pharmacology
Protein Kinases drug effects
Structure-Activity Relationship
Alkaloids pharmacology
Heterocyclic Compounds, 4 or More Rings pharmacology
Neoplasms drug therapy
Subjects
Details
- Language :
- English
- ISSN :
- 1660-3397
- Volume :
- 6
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Marine drugs
- Publication Type :
- Academic Journal
- Accession number :
- 19172192
- Full Text :
- https://doi.org/10.3390/md20080026