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Detection of Hereditary Prostate Cancer

Posted Nov 30 2008 4:00pm

Description of Invention:
Inherited prostate cancer susceptibility genes with high penetrance are responsible for 5% to 10% of all cancer cases and up to 30% to 40% of early onset of the disease. Previous genetic linkage studies indicated that germline variations in a gene or genes on Xq27 were involved in prostate carcinogenesis. The linkage peak for prostate cancer overlies a region containing five SPANX genes whose expression has been detected in a variety of cancers. The investigators have identified an intra-chromosomal inversion involving more than a 400 kb sequence in prostate cancer patients but not in unaffected individuals. This technology can be used as an accurate, early prostate cancer susceptibility diagnostics method.

Applications:
High throughput screening assay to predict patient susceptibility to prostate cancer

Advantages:
Easy, ready to use early stage prostate cancer diagnostic

Development Status:
The technology is currently in the pre-clinical stage of development.

Inventors:
Natalay Kouprina (NCI)


Licensing Status:
Available for licensing.


Portfolios:
Cancer
Cancer - Diagnostics
Gene Based Therapies
Gene Based Therapies - Diagnostics



For Additional Information Please Contact:
Jennifer Wong
NIH Office of Technology Transfer
6011 Executive Blvd. Suite 325,
Rockville, MD 20852
United States
Email: wongje@mail.nih.gov
Phone: 301-435-4633
Fax: 301-402-0220


Ref No: 1857

Updated: 12/2008

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