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Sermorelin

GHRH (1-29), GRF 1-29 NH2, Sermorelin acetate

Quick Stats
Studies 223
Trials 41
Score 2
2009 pubmed 11 citations

Stimulatory effect of growth hormone-releasing hormone (GHRH(1-29)NH2) on the proliferation, VEGF and chromogranin A secretion by human neuroendocrine tumor cell line NCI-H727 in vitro.

Stepień. Tomasz T; Sacewicz. Małgorzata M; Lawnicka. Hanna H; Krupiński. Roman R; Komorowski. Jan J; Siejka. Agnieszka A; Stepień. Henryk H

Key Findings

  • GHRH (1‑29)NH2 increased proliferation of NCI‑H727 neuroendocrine tumor cells in vitro
  • GHRH treatment raised VEGF secretion, a factor that promotes blood vessel growth
  • GHRH also boosted chromogranin A release, a marker of neuroendocrine activity

Practical Outcomes

  • If you’re using sermorelin or similar GHRH analogs, be aware there may be a risk of stimulating growth of hidden neuroendocrine tumors. Monitoring for tumor markers or avoiding use if you have a history of such cancers is prudent. This data doesn’t support any performance‑enhancing protocol with GHRH.

Summary

The study found that the hormone GHRH, which sermorelin mimics, can make certain lung neuroendocrine tumor cells grow faster and release more factors that promote blood vessel formation and tumor activity. This suggests that using GHRH‑like peptides could potentially stimulate tumor growth in susceptible tissues, so caution is advised for anyone considering them for anti‑aging or performance purposes.

Abstract

Growth hormone-releasing hormone (GHRH) and its receptors have been implicated in a variety of cellular processes like cell survival, proliferation, apoptosis, angiogenesis and neoplastic transformation of various non-pituitary tissues. Here, we investigated for the first time the in vitro effect of GHRH(1-29)NH2 on the proliferation and the secretion of vascular endothelial growth factor (VEGF) and chromogranin A by the human bronchial neuroendocrine tumor cells NCI-H727. GHRH(1-29)NH2 at the concentrations of 10(-8)-10(-6)M increased the proliferation of these cells and this effect was associated with a statistically significant increase in VEGF and chromogranin A secretion into the supernatants of the tested cells. Our findings indicate that GHRH functions as a trophic hormone for bronchial neuroendocrine (NET) tumors.

Study Information

Provider

pubmed

Year

2009

Date

2009-09-10T00:00:00.000Z

DOI

10.1016/j.npep.2009.08.005

Citations

11

References

46