Evidence map›Paper›PMID 28363699›Full record

ReviewBiochimica et biophysica acta. Molecular basis of disease2017

Bench-top to clinical therapies: A review of melanocortin ligands from 1954 to 2016.

Mark D Ericson, Cody J Lensing, Katlyn A Fleming, Katherine N Schlasner, Skye R Doering, Carrie Haskell-Luevano

Abstract readReview
In one paragraph

Review in Biochimica et biophysica acta. Molecular basis of disease, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

49 citing papers in PubMed.

  1. Trial
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  9. Carbocyclic setmelanotide analogs maintain biochemical potency at melanocortin 4 receptors.Journal of peptide science : an official publication of the European Peptide Society · 2025
    Article
  10. Article
  11. An overview of benefits and risks of chronic melanocortin-1 receptor activation.Journal of the European Academy of Dermatology and Venereology : JEADV · 2025
    Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Mark D EricsonDepartment of Medicinal Chemistry, University of Minnesota, Minneapolis, MN 55455, USA.
Cody J LensingDepartment of Medicinal Chemistry, University of Minnesota, Minneapolis, MN 55455, USA.
Katlyn A FlemingDepartment of Medicinal Chemistry, University of Minnesota, Minneapolis, MN 55455, USA.
Katherine N SchlasnerDepartment of Medicinal Chemistry, University of Minnesota, Minneapolis, MN 55455, USA.
Skye R DoeringDepartment of Medicinal Chemistry, University of Minnesota, Minneapolis, MN 55455, USA.
Carrie Haskell-LuevanoDepartment of Medicinal Chemistry, University of Minnesota, Minneapolis, MN 55455, USA. Electronic address: chaskell@umn.edu.

Funding

Melanocortin Selective LigandsR01DK091906 · NIDDK · UNIVERSITY OF MINNESOTA · PI HASKELL-LUEVANO, CARRIE · 2012 to 2015
$1.8M
Defensins as Melanocortin LigandsR01DK097838 · NIDDK · UNIVERSITY OF MINNESOTA · PI HASKELL-LUEVANO, CARRIE · 2013 to 2016
$1.7M
Novel Melanocortin Receptor Probe DiscoveryR01DK108893 · NIDDK · UNIVERSITY OF MINNESOTA · PI HASKELL-LUEVANO, CARRIE · 2016 to 2019
$1.5M
Molecular Probes of AGRP for Drug DiscoveryF32DK108402 · NIDDK · UNIVERSITY OF MINNESOTA · PI ERICSON, MARK · 2015 to 2018
$176k
NIDDK NIH HHS F32 DK108402NIDDK NIH HHS R01 DK091906NIDDK NIH HHS R01 DK097838NIDDK NIH HHS R01 DK108893
6 · The paper itself

Abstract

The discovery of the endogenous melanocortin agonists in the 1950s have resulted in sixty years of melanocortin ligand research. Early efforts involved truncations or select modifications of the naturally occurring agonists leading to the development of many potent and selective ligands. With the identification and cloning of the five known melanocortin receptors, many ligands were improved upon through bench-top in vitro assays. Optimization of select properties resulted in ligands adopted as clinical candidates. A summary of every melanocortin ligand is outside the scope of this review. Instead, this review will focus on the following topics: classic melanocortin ligands, selective ligands, small molecule (non-peptide) ligands, ligands with sex-specific effects, bivalent and multivalent ligands, and ligands advanced to clinical trials. Each topic area will be summarized with current references to update the melanocortin field on recent progress. This article is part of a Special Issue entitled: Melanocortin Receptors - edited by Ya-Xiong Tao.

Indexed as

Amino Acid SequenceAnimalsDrug DiscoveryHumansLigandsMelanocortinsModels, MolecularReceptors, MelanocortinSmall Molecule LibrariesLigandsMelanocortinsReceptors, MelanocortinSmall Molecule LibrariesBivalent/multivalent ligandsClinical trialsSelective ligandsSexual dimorphismSmall molecules

Identifiers

PMID28363699
PMCPMC5600687

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.