Licencing Opportunity:
This work represents a licensing opportunity.
The technology is available for licensing from TransGenex Nanobiotech Inc (a USF-spin-out) company.
Further Information:
NPRA has also been found to be a target in breast and prostate cancers. TransGenex Nanobiotech Inc is engaged in an aggressive program to obtain further patents on extensions of the technology it has developed. The company is now seeking a strategic partner to help finance Tox-Pharm studies leading to an Investigational New Drug application with the FDA and Phase I clinical trials.
Natriuretic peptide receptor a as a novel anticancer target.
Cancer research 2008 Jan 1; 68(1):249-56
Kong X X, Wang X X, Xu W W, Behera S S, Hellermann G G, Kumar A A, Lockey R RF, Mohapatra S S, Mohapatra S SS
Joy McCann Culverhouse Airway Disease and Nanomedicine Research Center, Allergy and Immunology Division, Department of Internal Medicine, University of South Florida College of Medicine, Tampa, FL 33612, USA.
The receptor for atrial natriuretic peptide (ANP), natriuretic peptide receptor A (NPRA), is expressed in cancer cells, and natriuretic peptides have been implicated in cancers. However, the direct role of NPRA signaling in tumorigenesis remains elusive. Here, we report that NPRA expression and signaling is important for tumor growth. NPRA-deficient mice showed significantly reduced antigen-induced pulmonary inflammation. NPRA deficiency also substantially protected C57BL/6 mice from lung, skin, and ovarian cancers. Furthermore, a nanoparticle-formulated interfering RNA for NPRA attenuated B16 melanoma tumors in mice. Ectopic expression of a plasmid encoding NP73-102, the NH(2)-terminal peptide of the ANP prohormone, which down-regulates NPRA expression, also suppressed lung metastasis of A549 cells in nude mice and tumorigenesis of Line 1 cells in immunocompetent BALB/c mice. The antitumor activity of NP73-102 was in part attributed to apoptosis of tumor cells. Western blot and immunohistochemistry staining indicated that the transcription factor, nuclear factor-kappaB, was inactivated, whereas the level of tumor suppressor retinoblastoma protein was up-regulated in the lungs of NPRA-deficient mice. Furthermore, expression of vascular endothelial growth factor was down-regulated in the lungs of NPRA-deficient mice compared with that in wild-type mice. These results suggest that NPRA is involved in tumor angiogenesis and represents a new target for cancer therapy.
Keywords: Natriuretic peptide ANP NPRA