Evidence map›Paper›PMID 27547198›Full record

ReviewFrontiers in endocrinology2016

ACTH Antagonists.

Adrian John Clark, Rachel Forfar, Mashal Hussain, Jeff Jerman, Ed McIver, Debra Taylor, Li Chan

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in endocrinology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

14 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Article
  3. Effects of ACTHBulletin of experimental biology and medicine · 2025
    Article
  4. Review
  5. Article
  6. Advances in pharmacological treatment of CushingZhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2024
    Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
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

7 authors at 2 institutions in 1 country.

Adrian John ClarkCentre for Endocrinology, William Harvey Research Institute, Queen Mary University of London , London , UK.
Rachel ForfarCentre for Therapeutics Discovery, MRC Technology , Stevenage , UK.
Mashal HussainCentre for Endocrinology, William Harvey Research Institute, Queen Mary University of London , London , UK.
Jeff JermanCentre for Therapeutics Discovery, MRC Technology , Stevenage , UK.
Ed McIverCentre for Therapeutics Discovery, MRC Technology , Stevenage , UK.
Debra TaylorCentre for Therapeutics Discovery, MRC Technology , Stevenage , UK.
Li ChanCentre for Endocrinology, William Harvey Research Institute, Queen Mary University of London , London , UK.
LifeArc · GBQueen Mary University of London · GB

Funding

Medical Research Council G0802796Medical Research Council MC_G1000806
6 · The paper itself

Abstract

Adrenocorticotropin (ACTH) acts via a highly selective receptor that is a member of the melanocortin receptor subfamily of type 1 G protein-coupled receptors. The ACTH receptor, also known as the melanocortin 2 receptor (MC2R), is unusual in that it is absolutely dependent on a small accessory protein, melanocortin receptor accessory protein (MRAP) for cell surface expression and function. ACTH is the only known naturally occurring agonist for this receptor. This lack of redundancy and high degree of ligand specificity suggests that antagonism of this receptor could provide a useful therapeutic aid and a potential investigational tool. Clinical situations in which this could be useful include (1) Cushing's disease and ectopic ACTH syndrome - especially while preparing for definitive treatment of a causative tumor, or in refractory cases, or (2) congenital adrenal hyperplasia - as an adjunct to glucocorticoid replacement. A case for antagonism in other clinical situations in which there is ACTH excess can also be made. In this article, we will explore the scientific and clinical case for an ACTH antagonist, and will review the evidence for existing and recently described peptides and modified peptides in this role.

Indexed as

adrenocorticotropin hormonecongenital adrenal hyperplasiaCushing’s syndromeG protein-coupled receptorhigh throughput screeningpeptide hormone antagonistsreceptor antagonismreceptor modelling

Identifiers

PMID27547198
PMCPMC4974254
OpenAlexW4210396070

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.