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Sermorelin

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

Quick Stats
Studies 223
Trials 41
Score 1
2024 pubmed 2 citations

A novel approach for the treatment of AML, through GHRH antagonism: MIA-602.

Costoya. Joel J; Gaumond. Simonetta I SI; Chale. Ravinder S RS; Schally. Andrew V AV; Jimenez. Joaquin J JJ

Key Findings

  • GHRH antagonists like MIA-602 kill AML cancer cells in vitro and in animal models
  • MIA-602 works against drug‑resistant leukemia cells
  • When combined with standard chemotherapy, MIA-602 shows synergistic anti‑cancer effects

Practical Outcomes

  • For biohackers, this research is not actionable yet; it highlights a potential future AML therapy but offers no safe, self‑administered protocol or dosage. The findings are mainly of interest for clinical development rather than personal health optimization.

Summary

The study looks at a new drug called MIA-602 that blocks a hormone signal (GHRH) and shows it can kill leukemia cells in lab tests, even those that resist standard chemo, and works better when combined with chemo. However, this is early‑stage cancer research, not a health‑boosting supplement, and it isn’t ready for personal use.

Abstract

Acute myeloid leukemia (AML) is the most aggressive and prevalent form of leukemia in adults. The gold-standard intervention revolves around the use of chemotherapy, and in some cases hematopoietic stem cell transplantation. Drug resistance is a frequent complication resulting from treatment, as it stands there are limited clinical measures available for refractory AML besides palliative care. The goal of this review is to renew interest in a novel targeted hormone therapy in the treatment of AML utilizing growth hormone-releasing hormone (GHRH) antagonism, given it may provide a potential solution for current barriers to achieving complete remission post-therapy. Recapitulating pre-clinical evidence, GHRH antagonists (GHRH-Ant) have significant anti-cancer activity across experimental human AML cell lines in vitro and in vivo and demonstrate significant inhibition of cancer in drug resistant analogs of leukemic cell lines as well. GHRH-Ant act in manners that are orthogonal to anthracyclines and when administered in combination synergize to produce a more potent anti-neoplastic effect. Considering the adversities associated with standard AML therapies and the developing issue of drug resistance, MIA-602 represents a novel approach worth further investigation.

Study Information

Provider

pubmed

Year

2024

Date

2024-10-17T00:00:00.000Z

DOI

10.1007/s11154-024-09917-6

Citations

2

References

58