Urodilatin and four cardiac hormones decrease human renal carcinoma cell numbers
B A Vesely1, E J Eichelbaum, A A Alli
1James A. Haley Veterans Medical Center and University of South Florida Health Sciences Center, Tampa, 33612, USA.
Background:
Mortality from renal-cell cancer remains a significant problem with an estimated 12,600 deaths in the United States in 2005 even with current treatment(s) of surgery, chemotherapy, radiation and immunotherapy. Four cardiac natriuretic peptides, that is, atrial natriuretic peptide, vessel dilator, long-acting natriuretic peptide and kaliuretic peptide have significant anti-cancer effects in breast, pancreatic, prostate and colon adenocarcinomas.
Materials And Methods:
These four peptide hormones plus brain natriuretic peptide (BNP), C-natriuretic peptide (CNP) and urodilatin, a peptide hormone formed in the kidney by a different post-translational processing of the atrial natriuretic peptide prohormone, were evaluated for their anti-cancer effects in renal carcinomas.
Results:
Dose-response curves revealed a significant (P < 0.0001) decrease in human renal carcinoma cells with each 10-fold increase in concentration from 1 microm to 100 microm of five of these peptide hormones. There was an 81%, 74%, 66%, 70% and 70% elimination within 24 h in renal carcinoma cells secondary to vessel dilator, kaliuretic peptide, urodilatin, atrial natriuretic peptide and long-acting natriuretic peptide, respectively (P < 0.0001 for each), whereas BNP had no effect and CNP decreased renal cancer cell number by 10% (P = 0.04) at their 100 microm concentrations. Three days after treatment with these peptide hormones, the cancer cells began to proliferate again. The four cardiac hormones and urodilatin decreased DNA synthesis from 65-84% (P < 0.00001), whereas BNP and CNP decreased DNA synthesis 3% and 12% (both non-significant). Western blots revealed for the first time natriuretic peptide receptors (NPR)-A, -B and -C were present in the renal cancer cells.
Conclusions:
These results indicate that urodilatin and the four cardiac hormones have potent anti-cancer effects by eliminating up to 81% of renal carcinoma cells within 24 h of treatment.
Insights
Natriuretic peptides, including urodilatin and four cardiac hormones, show potent anti-cancer effects against renal carcinoma cells. These peptide hormones eliminated up to 81% of cancer cells within 24 hours, offering a promising new avenue for cancer treatment.
Area of Science:
- Cardiovascular Endocrinology
- Nephrology
- Oncology
Background:
- Renal-cell cancer (RCC) poses a significant mortality risk, with limited success from current treatments.
- Four cardiac natriuretic peptides have demonstrated anti-cancer properties in various adenocarcinomas.
Purpose of the Study:
- To evaluate the anti-cancer effects of several natriuretic peptides and urodilatin in renal carcinomas.
- To investigate the presence of natriuretic peptide receptors in renal cancer cells.
Main Methods:
- Seven peptide hormones (atrial natriuretic peptide, vessel dilator, long-acting natriuretic peptide, kaliuretic peptide, brain natriuretic peptide (BNP), C-natriuretic peptide (CNP), and urodilatin) were tested.
- Dose-response studies and DNA synthesis assays were performed on human renal carcinoma cells.
- Western blotting was used to detect natriuretic peptide receptors (NPRs).
Main Results:
- Vessel dilator, kaliuretic peptide, urodilatin, atrial natriuretic peptide, and long-acting natriuretic peptide significantly reduced renal carcinoma cell count by up to 81% within 24 hours.
- BNP showed no effect, while CNP had a minimal effect on cell number.
- These peptide hormones, along with urodilatin, significantly decreased DNA synthesis (65-84%).
- Natriuretic peptide receptors (NPR-A, -B, and -C) were detected in renal cancer cells.
Conclusions:
- Urodilatin and four cardiac hormones exhibit potent anti-cancer activity against renal carcinoma cells.
- These findings suggest a potential therapeutic role for specific natriuretic peptides in RCC treatment.
- The presence of NPRs indicates a mechanism for peptide hormone action in renal cancer cells.
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