Research profile · Peptide
MGF
Also known as Mechano growth factor, IGF-1Ec E-domain peptide
Overview
A peptide from a splice variant of IGF-1 whose foundational finding failed independent replication.
- Category
- Peptide
- Highest evidence level identified
- Animal evidence
- Last scientifically reviewed
- 20 August 2026
- Last regulatory review
- 20 August 2026
Mechanism under investigation
MGF is the C-terminal E-domain peptide of a splice variant of insulin-like growth factor 1 that is upregulated in skeletal muscle after mechanical loading or damage. It has been proposed that this peptide acts distinctly from mature IGF-1 by activating quiescent satellite cells and promoting myoblast proliferation while delaying fusion. That proposal is contested: a 2014 replication attempt by two pharmaceutical companies failed to reproduce the effect and concluded that the findings call into question whether the peptide has a physiological role at all.
Research areas
- Muscle biology
- Growth factor signalling
These are fields in which the compound has been investigated. Listing a field is not a statement that anything was demonstrated within it.
Current evidence
In-vitro evidence
Cells, tissues or biochemical systems outside a living organism.
Present but contradictory, and the contradiction is the important part. The original 2002 work reported that the E-domain peptide affected myoblast proliferation and differentiation differently from mature IGF-1. A 2014 replication attempt across four separate cell systems found the peptide failed to increase proliferation, failed to inhibit differentiation and failed to activate the expected signalling — while mature IGF-1 produced robust responses in the same systems.
- Different roles of the IGF-I Ec peptide and mature IGF-I in myoblast proliferation and differentiation (opens doi.org in a new tab)
- Mechano-growth factor peptide, the COOH terminus of unprocessed insulin-like growth factor 1, has no apparent effect on myoblasts or primary muscle stem cells (opens doi.org in a new tab)
Animal evidence
Studies in living non-human animals.
Limited and mostly low-citation. Rodent and rabbit studies exist, but much of the animal literature measures endogenous expression rather than administering the peptide. No large or replicated efficacy programme was located.
Human observational evidence
Studies observing people without assigning an intervention.
Exists, but only for endogenous expression rather than administration. Human muscle biopsy work has measured splice-variant messenger RNA after resistance exercise. The peptide was measured, never given.
Clinical-trial evidence
Studies assigning an intervention to human participants.
None. No registered interventional study was found, and a search of the indexed literature returned no human interventional trial.
Study limitations
- The foundational satellite-cell finding failed independent replication in a well-powered multi-system attempt by two separate pharmaceutical companies.
- No human has ever been administered this peptide in a registered trial. All human data concern endogenous expression after exercise.
- Much of the supporting literature comes from a single research lineage, which limits evidential independence.
- Animal studies are heterogeneous in species, model and endpoint, with small samples and no replication programme.
UK regulatory context
Experimental — not authorised for human use in the UK
A compound appearing in research literature that holds no UK authorisation for human use in any indication.
Source: The Human Medicines Regulations 2012, regulation 46 — prohibition on sale or supply of an unauthorised medicinal product (opens legislation.gov.uk in a new tab) (legislation.gov.uk)
Regulatory classification is jurisdiction-specific. A compound authorised elsewhere is not thereby authorised in the UK, and a supplier’s description of a substance does not determine how it is classified in law. See safety and regulation for the framework and the authoritative sources.
Safety and interpretation
No safety data from controlled human administration exist, because no such study has been conducted. Because the peptide sits on the IGF-1 axis, mitogenic concerns are biologically plausible but unproven and unquantified. Material supplied outside a regulated chain has no assured composition or purity.
References
- Regulator or official body
legislation.gov.uk, 2012 · accessed 20 August 2026
No UK marketing authorisation. The electronic Medicines Compendium ingredient index lists mecasermin, which is recombinant IGF-1 and a different molecule, but contains no entry for this peptide.
- Primary researchCitation not yet verified
Fornaro M, et al.. American Journal of Physiology: Endocrinology and Metabolism, 2014 · doi:10.1152/ajpendo.00408.2013
The replication failure. Bibliographic record confirmed via Europe PMC and the DOI verified as registered via Crossref.
- Primary researchCitation not yet verified
Yang SY, Goldspink G. FEBS Letters, 2002 · doi:10.1016/S0014-5793(02)02918-6
The original finding. Bibliographic record confirmed via Europe PMC.
- Primary researchCitation not yet verified
Hameed M, et al.. Journal of Physiology, 2003 · doi:10.1113/jphysiol.2002.032136
Measured endogenous expression; the peptide was not administered. Bibliographic record confirmed via NCBI E-utilities.