Use of the TP5 Peptide for the Treatment of Cancer

GBM is the most aggressive form of brain cancer. The current standard of care against GBM is a combination of surgery, chemotherapy and radiotherapy. However, after standard treatment, the cancer usually recurs – emphasizing a need for new targets and better alternatives. A promising target is cyclin-dependent kinase 5 (CDK5), the hyperactivity of which has been shown to have a role in cancer progression. 

TP5/TFP5, a small peptide inhibitor against CDK5, was developed at the National Institutes of Health and modified to increase its passage through the blood brain barrier. Researchers at the NCI and NINDS demonstrated that TP5 decreases cell viability and increases programmed cell death in GBM and CRC cell lines with aberrant CDK5 activity. TP5 was found to impair DNA repair by inhibiting CDK5 and acted additively and synergistically with DNA-damaging agents (e.g. temozolomide, irinotecan, irradiation) used in treatment of GBM and colon carcinoma. TP5 decreased the tumor volume and increased the overall survival of orthotopic glioblastoma mouse models.

The Neuro-Oncology Branch is seeking statements of capability or interest from parties interested in licensing this invention to further develop, evaluate, or commercialize TP5 for novel treatment of GBM and/or other cancers with aberrant CDK5 expression.

Potential Commercial Applications:		Competitive Advantages:
Treatment of GBM and other brain tumors with aberrant CDK5 expression Treatment of other cancers with aberrant CDK5 expression, including CRC and lung cancer The GBM market is expected to grow to >U$1B at a compound annual growth rate (CAGR) of 7.5% The CRC market has risen to >US$8B at a CAGR of 3%		TP5: Decreases the tumor volume and the proliferation rate of GBM in mouse models Can cross the blood-brain barrier, overcoming a major obstacle for the therapeutic agent development for GBM Decreases the tumor volume in CRC mouse models Additive as well as synergistic with the current standard of care CDK5: CDK5 expression and activity are deregulated in cancer cells; because CDK5 is not a tumor-associated mutation, the role of CDK5 in cancer has been underappreciated until recently – meaning less competition Roscovitine, another CDK inhibitor, was shown to delay resistance to temozolomide – the only approved drug for GBM

Development Stage:
Pre-clinical (in vivo)

Related Invention(s):
E-144-2010


Inventors:

Zhengping Zhuang (NCI)  ➽ more inventions...

Emeline Tabouret (NCI)  ➽ more inventions...

Herui Wang (NCI)  ➽ more inventions...

Harish Pant (NINDS)  ➽ more inventions...

Niranjana Amin (NINDS)  ➽ more inventions...


Intellectual Property:
Pat: - issued -

Publications:
Tabouret E, et al. TP5, a peptide inhibitor of aberrant and hyperactive CDK5/p25: a novel therapeutic approach against glioblastoma.  Oxford Academic
Binukumar BK, et al. TFP5/TP5 peptide provides neuroprotection in the MPTP model of Parkinson’s disease.  PMID: 27335538
Binukumar BK, et al. Peptide TFP5/TP5 derived from Cdk5 activator P35 provides neuroprotection in the MPTP model of Parkinson’s disease.  PMID: 26399293

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-007-2019
Updated: Oct 6, 2020