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Recent Advances in the Therapeutic Perspectives of Nutlin-3

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Nutlin-3 is a small molecule inhibitor of the MDM2/p53 interaction, which leads to the non-genotoxic p53 stabilization, activation of cell cycle arrest and apoptosis pathways. A series of recent studies have strengthened the concept that selective, non-genotoxic p53 activation by Nutlin-3 might represent an alternative to the current cytotoxic chemotherapy, in particular for pediatric tumors and for hematological malignancies, which retain a high percentage of p53wild-type status at diagnosis. Like most other drugs employed in cancer therapy, it will be unlikely that Nutlin-3 will be used as a monotherapy. In this respect, Nutlin-3 shows a synergistic cytotoxic effect when used in combination with innovative drugs, such as TRAIL or bortozemib. Although Nutlin-3 is currently in phase I clinical trial for the treatment of retinoblastoma, its effects on normal tissues and cell types remain largely to be determined and will require further investigation in the future years.





Keywords: HDM2; MDM2; Nutlin-3; P-gp; PEDIATRIC TUMORS; Pediatric malignancies; apoptosis; autophagic; chemotherapy; endothelial; hematological malignancies; leukemia; malignancies; p53 pathway; p53-independent; pharmacokinetics; senescence; synergistic; therapeutic combinations

Document Type: Research Article

Publication date: 01 February 2011

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    Each thematic issue of Current Pharmaceutical Design covers all subject areas of major importance to modern drug design, including: medicinal chemistry, pharmacology, drug targets and disease mechanism.
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