Evidence map›Paper›PMID 35665216›Full record

ArticleSkin health and disease2022

Melanogenic effect of dersimelagon (MT-7117), a novel oral melanocortin 1 receptor agonist.

T Suzuki, Y Kawano, A Matsumoto, M Kondo, K Funayama, S Tanemura, M Miyashiro, A Nishi, K Yamada, M Tsuda and 3 more

Open access · goldAbstract read
In one paragraph

Article in Skin health and disease, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.8field-weighted citation impact, top 15% of its field
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

12 citing papers in PubMed, 21 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. An overview of benefits and risks of chronic melanocortin-1 receptor activation.Journal of the European Academy of Dermatology and Venereology : JEADV · 2025
    Review
  6. Review
  7. Review
  8. Melanocortin 1 Receptor (MC1R): Pharmacological and Therapeutic Aspects.International journal of molecular sciences · 2023
    Review
  9. Absorption, metabolism, and excretion of [Pharmacology research & perspectives · 2023
    Article
  10. Review
  11. Article
  12. Article
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

13 authors at 1 institution in 1 country.

T SuzukiSohyaku Innovative Research Division Mitsubishi Tanabe Pharma Corporation Yokohama Japan.ORCID https://orcid.org/0000-0002-4902-2927
Y KawanoSohyaku Innovative Research Division Mitsubishi Tanabe Pharma Corporation Yokohama Japan.
A MatsumotoSohyaku Innovative Research Division Mitsubishi Tanabe Pharma Corporation Yokohama Japan.
M KondoSohyaku Innovative Research Division Mitsubishi Tanabe Pharma Corporation Yokohama Japan.
K FunayamaSohyaku Innovative Research Division Mitsubishi Tanabe Pharma Corporation Yokohama Japan.
S TanemuraSohyaku Innovative Research Division Mitsubishi Tanabe Pharma Corporation Yokohama Japan.
M MiyashiroSohyaku Innovative Research Division Mitsubishi Tanabe Pharma Corporation Yokohama Japan.
A NishiSohyaku Innovative Research Division Mitsubishi Tanabe Pharma Corporation Yokohama Japan.
K YamadaSohyaku Innovative Research Division Mitsubishi Tanabe Pharma Corporation Yokohama Japan.
M TsudaSohyaku Innovative Research Division Mitsubishi Tanabe Pharma Corporation Yokohama Japan.
A SatoSohyaku Innovative Research Division Mitsubishi Tanabe Pharma Corporation Yokohama Japan.
K MorokumaSohyaku Innovative Research Division Mitsubishi Tanabe Pharma Corporation Yokohama Japan.
Y YamamotoSohyaku Innovative Research Division Mitsubishi Tanabe Pharma Corporation Yokohama Japan.
Mitsubishi Group (Japan) · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The activation of melanocortin 1 receptor (MC1R) on melanocytes stimulates the production of eumelanin. A tridecapeptide α melanocyte-stimulating hormone (αMSH) is known to induce skin pigmentation. Objectives: We characterised the properties of a novel oral MC1R agonist dersimelagon (MT-7117) with respect to its specific binding to MC1R, downstream signalling and eumelanin production in experimental models. Methods: The competitive binding and production of intracellular cyclic adenosine 3', 5'-monophosphate in cells expressing recombinant melanocortin receptors were examined. A mouse melanoma cell line B16F1 was used for the evaluation of in vitro melanin production. The in vitro activity of MT-7117 was determined with αMSH and [Nle Results: MT-7117 showed the highest affinity for human MC1R compared to the other melanocortin receptors evaluated and agonistic activity for human, cynomolgus monkey and mouse MC1R, with EC Conclusions: MT-7117 is a novel oral MC1R agonist that induces melanogenesis in vitro and in vivo, suggesting its potential application for the prevention of phototoxic reactions in patients with photodermatoses, such as erythropoietic protoporphyria and X-linked protoporphyria.

Identifiers

PMID35665216
PMCPMC9060023
OpenAlexW3216575265

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Registered trials

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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.