Natriuretic peptide receptor a as a novel target for prostate cancer

• Published in: Molecular cancer 2011-05, Vol.10 (1), p.56-56, Article 56
• Main Authors: Wang, Xiaoqin, Raulji, Payal, Mohapatra, Shyam S, Patel, Ronil, Hellermann, Gary, Kong, Xiaoyuan, Vera, Pedro L, Meyer-Siegler, Katherine L, Coppola, Domenico, Mohapatra, Subhra
• Format: Article
• Language: English
• Subjects: Animals; Apoptosis; Care and treatment; Cell Line; Diagnosis; Disease Progression; Down-Regulation; Humans; Intramolecular Oxidoreductases - metabolism; Macrophage Migration-Inhibitory Factors - metabolism; Male; Mice; Mice, Inbred C57BL; Mice, Knockout; Natriuretic peptides; Peptides - genetics; Peptides - metabolism; Physiological aspects; Prostate cancer; Prostatic Neoplasms - physiopathology; Rabbits; Rats; Receptors, Atrial Natriuretic Factor - antagonists & inhibitors; Receptors, Atrial Natriuretic Factor - genetics; Receptors, Atrial Natriuretic Factor - metabolism; RNA, Small Interfering - metabolism; Tumor Burden - genetics; Xenograft Model Antitumor Assays
• ISSN: 1476-4598; 1476-4598
• DOI: 10.1186/1476-4598-10-56

The receptor for the cardiac hormone 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 prostate cancer remains unclear. NPRA expression was examined by western blotting, RT-PCR and immunohistochemistry. NPRA was downregulated by transfection of siRNA, shRNA and NPRA inhibitor (iNPRA). Antitumor efficacy of iNPRA was tested in mice using a TRAMP-C1 xenograft. Here, we demonstrated that NPRA is abundantly expressed on tumorigenic mouse and human prostate cells, but not in nontumorigenic prostate epithelial cells. NPRA expression showed positive correlation with clinical staging in a human PCa tissue microarray. Down-regulation of NPRA by siNPRA or iNPRA induced apoptosis in PCa cells. The mechanism of iNPRA-induced anti-PCa effects was linked to NPRA-induced expression of macrophage migration inhibitory factor (MIF), a proinflammatory cytokine over-expressed in PCa and significantly reduced by siNPRA. Prostate tumor cells implanted in mice deficient in atrial natriuretic peptide receptor A (NPRA-KO) failed to grow, and treatment of TRAMP-C1 xenografts with iNPRA reduced tumor burden and MIF expression. Using the TRAMP spontaneous PCa model, we found that NPRA expression correlated with MIF expression during PCa progression. Collectively, these results suggest that NPRA promotes PCa development in part by regulating MIF. Our findings also suggest that NPRA is a potential prognostic marker and a target for PCa therapy.