Evidence map›Paper›PMID 37428391›Full record

ReviewProtein science : a publication of the Protein Society2023

Growth hormone receptor agonists and antagonists: From protein expression and purification to long-acting formulations.

Yue Wang, Minah Kim, Chantal Buckley, Heather D Maynard, Ries J Langley, Jo K Perry

Open access · hybridAbstract readReview
In one paragraph

Review in Protein science : a publication of the Protein Society, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.6field-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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
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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 at 2 institutions in 2 countries.

Yue WangLiggins Institute, University of Auckland, Auckland, New Zealand.ORCID 0000-0001-9010-4177
Minah KimLiggins Institute, University of Auckland, Auckland, New Zealand.
Chantal BuckleyLiggins Institute, University of Auckland, Auckland, New Zealand.
Heather D MaynardDepartment of Chemistry and Biochemistry and the California NanoSystems Institute, University of California, Los Angeles, California, USA.
Ries J LangleyMaurice Wilkins Centre for Molecular Biodiscovery, Auckland, New Zealand.
Jo K PerryLiggins Institute, University of Auckland, Auckland, New Zealand.
University of Auckland · NZCalifornia NanoSystems Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recombinant human growth hormone (rhGH) and GH receptor antagonists (GHAs) are used clinically to treat a range of disorders associated with GH deficiency or hypersecretion, respectively. However, these biotherapeutics can be difficult and expensive to manufacture with multiple challenges from recombinant protein generation through to the development of long-acting formulations required to improve the circulating half-life of the drug. In this review, we summarize methodologies and approaches used for making and purifying recombinant GH and GHA proteins, and strategies to improve pharmacokinetic and pharmacodynamic properties, including PEGylation and fusion proteins. Therapeutics that are in clinical use or are currently under development are also discussed.

Indexed as

Human Growth HormoneReceptors, SomatotropinHumansRecombinant ProteinsHuman Growth HormoneReceptors, SomatotropinRecombinant Proteinsantagonistbiotherapeuticfusion proteingrowth hormonelong-actingPEGylationrecombinant protein production

Identifiers

PMID37428391
PMCPMC10443362
OpenAlexW4383710780

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.