Evidence map›Paper›PMID 35647546›Full record

ReviewRSC medicinal chemistry2022

Recent developments in the structural characterisation of the IR and IGF1R: implications for the design of IR-IGF1R hybrid receptor modulators.

Samuel J Turvey, Martin J McPhillie, Mark T Kearney, Stephen P Muench, Katie J Simmons, Colin W G Fishwick

Open access · hybridAbstract readReview
In one paragraph

Review in RSC medicinal chemistry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

10 citing papers in PubMed, 23 citations in OpenAlex.

  1. NovelJournal of clinical research in pediatric endocrinology · 2026
    Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. The Role of SOX9 in IGF-II-Mediated Pulmonary Fibrosis.International journal of molecular sciences · 2023
    Article
  8. Article
  9. Article
  10. 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

6 authors at 1 institution in 1 country.

Samuel J TurveyLeeds Institute for Cardiovascular and Metabolic Medicine, University of Leeds UK K.J.Simmons@leeds.ac.uk.ORCID https://orcid.org/0000-0003-4298-8339
Martin J McPhillieSchool of Chemistry, University of Leeds UK C.W.G.Fishwick@leeds.ac.uk.ORCID https://orcid.org/0000-0001-8264-8211
Mark T KearneyLeeds Institute for Cardiovascular and Metabolic Medicine, University of Leeds UK K.J.Simmons@leeds.ac.uk.
Stephen P MuenchSchool of Biomedical Sciences, Faculty of Biological Sciences & Astbury Centre, University of Leeds UK.ORCID https://orcid.org/0000-0001-6869-4414
Katie J SimmonsLeeds Institute for Cardiovascular and Metabolic Medicine, University of Leeds UK K.J.Simmons@leeds.ac.uk.ORCID https://orcid.org/0000-0003-4846-9097
Colin W G FishwickSchool of Chemistry, University of Leeds UK C.W.G.Fishwick@leeds.ac.uk.
University of Leeds · GB

Funding

British Heart Foundation CH/13/1/30086British Heart Foundation PG/18/82/34120British Heart Foundation RG/15/7/31521
6 · The paper itself

Abstract

The insulin receptor (IR) and insulin-like growth factor 1 receptor (IGF1R) are dimeric disulfide-linked receptor tyrosine kinases, whose actions regulate metabolic and mitogenic signalling pathways inside the cell. It is well documented that in tissues co-expressing the IR and IGF1R, their respective monomers can heterodimerise to form IR-IGF1R hybrid receptors. Increased populations of the IR-IGF1R hybrid receptors are associated with several disease states, including type 2 diabetes and cancer. Recently, progress in the structural biology of IR and IGF1R has given insights into their structure-function relationships and mechanism of action. However, challenges in isolating IR-IGF1R hybrid receptors mean that their structural properties remain relatively unexplored. This review discusses the advances in the structural understanding of the IR and IGF1R, and how these discoveries can inform the design of small-molecule modulators of the IR-IGF1R hybrid receptors to understand their role in cell biology.

Identifiers

PMID35647546
PMCPMC9020618
OpenAlexW4213335178

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.