Highly Soluble Pyrimido-Dione-Quinoline Compounds: Small Molecules that Stabilize and Activate p53 in Transformed Cells

The tumor-suppressor p53 protein plays a major role in tumor development. Most human cancers fail to normally activate wild-type p53, which is at least partly responsible for the unregulated growth of cancer cells and their failure to undergo apoptosis. While many chemotherapeutics enhance p53 levels, their non-specific DNA damage (genotoxicity) causes unfavorable side effects.
Defects in the pathways that control the stabilization and activation of p53 in response to stress can contribute to cancer development, without the requirement for mutation within the p53 gene itself. Many tumors that retain wild-type p53 show evidence of alterations that prevent efficient activation of p53 in response to stress, linked to a failure to inactivate HDM2. In these tumors, inhibition of HDM2 and reactivation of p53 is an attractive therapeutic strategy. Researchers at the National Cancer Institute (NCI) have developed a water-soluble, small molecule inhibitor of HDM2’s E3 activity resulting in activation of p53 in tumors that retain wild-type p53.

This invention does not lead to the genotoxicity commonly observed when using other therapeutics directed at activating p53, making it an attractive option for cancer therapy. The NCI is seeking statements of capability or interest from parties interested in licensing or in collaborative research to co-develop technologies that inhibit HDM2’s activity and reactivate p53 activity for the treatment of cancer.

Potential Commercial Applications: Competitive Advantages:
  • Targeted therapies for activating wild-type p53 in tumors to induce apoptosis
  • Inhibits unregulated growth of cancer cells
  • Reduced genotoxicity compared to many chemotherapeutics
  • Water-soluble with improved potency in stabilizing p53 and activating a p53 response

Development Stage:
Discovery (Lead Identification)

Related Invention(s):


Alan Weissman (NCI)  ➽ more inventions...

Yili Yang

Intellectual Property:
U.S. Pat: 8,877,765 issued 2014-11-04
Application No. PCT/US2007/013952
Application No. 8,877,765

Yang Y et al. Small molecule inhibitors of HDM2 ubiquitin ligase activity stabilize and activate p53 in cells  PMID 15950904

Collaboration Opportunity:

Licensing and research collaboration

Licensing Contact:
John Hewes, Ph.D.
Email: John.Hewes@nih.gov
Phone: 240-276-5515

OTT Reference No: E-138-2006
Updated: Oct 12, 2018