6533b81ffe1ef96bd1278e58
RESEARCH PRODUCT
Dérivé de la bléomycine générant moins de ROS ? Moins de fibrose ? Une alternative dans le développement d’une thérapie anticancéreuse efficace mais moins toxique
A KenaniAli BettaiebAli BettaiebS Brahimsubject
Drugcongenital hereditary and neonatal diseases and abnormalitiesCancer Researchurogenital systemmedia_common.quotation_subjectnutritional and metabolic diseasesHematologyGeneral MedicineBleomycinmedicine.diseaseMolecular biologychemistry.chemical_compoundOncologychemistryMechanism of actionApoptosisFibrosisPulmonary fibrosisToxicitymedicineRadiology Nuclear Medicine and imagingmedicine.symptomCytotoxicitymedia_commondescription
Deglycobleomycin (DBLM), the aglycon of the glycopeptide antitumor drug bleomycin (BLM), was first used since 1980 during comparative studies between BLM and DBLM in order to elucidate the role of the sugar component in the mechanism of action of BLM. In fact, the deglycosylation of BLM reduce the toxicity of this molecule and fails to produce reactive oxygen species, responsible for pulmonary fibrosis, and for anti-neoplastic activity of BLM. This causes toxic DNA lesions and ultimately leads to cell death. The therapeutic use of BLM is limited by a dose-dependent lung toxicity that eventually leads to fibrosis. Testing BLM-derivative molecules and defining their molecular mechanisms involved in tumor cell death may help to design new therapeutic approach with limited toxicity profile while maintaining anti-tumoral properties. The present review was undertaken to determine the effect of carbohydrate moiety in the mechanism of BLM induced cytotoxicity behind a comparative studies between BLM and DBLM.
year | journal | country | edition | language |
---|---|---|---|---|
2010-05-01 | Bulletin du Cancer |