Publication Date:
2016
abstract:
Introduction: Restoration of the p53 tumor suppressor function is an attractive anticancer strategy. Despite the development of several therapeutics targeting the two main p53 negative regulators, MDM2 and MDM4, no one has yet reached clinical application. In the past, several efforts have been employed to develop more specific and efficient compounds that can improve and/or overcome some of the features related to small molecule compounds (SMC). Peptides and peptidomimetics are emerging as attractive molecules given their increased selectivity, reduced toxicity and reduced tendency to develop tumor-resistance compared to SMC.
Iris type:
01.01 Articolo in rivista
Keywords:
p53 reactivation therapy; anticancer peptide; MDM2; MDM4; MDMX; dual-inhibitor; therapy-resistance
List of contributors:
Pellegrino, Marsha; Teveroni, Emanuela; Luca', Rossella; Moretti, Fabiola
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