Development of Novel p16INK4a Mimetics as Anticancer Therapy

Abstract

Mesothelioma therapy is a highly fatal disease that has poorly effective therapy with dose-limiting side-effects. Low expression of the CDK4/CDK6 inhibitor p16INK4a has been demonstrated in up to 90% of mesothelioma tumors. The objective of this application as a next step in the pursuit of this long term goal is to identify stabilized peptides that will mimic the interaction between p16INK4a and CDK4/6. The central hypothesis of this proposal is that protein-protein interactions can be replicated or disrupted by stabilized peptides that have been identified via the identification of pharmacophores of small peptides that interact with CDK4/6. The specific aims are as follows. (1) Determine structure-function relationships of overlapping peptides derived from p16INK4a that inhibit the activity of CDK4/6 and identify stabilized peptides that inhibit CDK4/6. (2) In vitro functional studies will be used to evaluate bioactivities of stabilized peptides. (3) In vitro ADME studies to evaluate the cell permeability, delivery, and efficacy of stabilized peptides.

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Document Details

Document Type
Technical Report
Publication Date
Oct 01, 2015
Accession Number
AD1003806

Entities

People

  • Mark Klein

Tags

DTIC Thesaurus Topics

  • Cell Line
  • Cell Physiological Processes
  • Chemical Synthesis
  • Chemistry
  • Clinical Trials
  • Gene Therapy
  • Identification
  • Inhibitors
  • Medical Personnel
  • Mesothelioma
  • Molecular Dynamics
  • Neoplasms
  • Protein-Protein Interactions
  • Side Effects
  • Simulations
  • Therapy
  • Three Dimensional

Readers

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