Evidence map›Paper›PMID 32942611›Full record

ReviewDiseases (Basel, Switzerland)2020

Glycoprotein G-protein Coupled Receptors in Disease: Luteinizing Hormone Receptors and Follicle Stimulating Hormone Receptors.

Duaa Althumairy, Xiaoping Zhang, Nicholas Baez, George Barisas, Deborah A Roess, George R Bousfield, Debbie C Crans

Open access · goldAbstract readReview
In one paragraph

Review in Diseases (Basel, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

13 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Significance ofInternational journal of reproductive biomedicine · 2024
    Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. 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

7 authors at 3 institutions in 2 countries.

Duaa AlthumairyCell and Molecular Biology Program, Colorado State University, Fort Collins, CO 80523, USA.
Xiaoping ZhangDepartment of Chemistry, Colorado State University, Fort Collins, CO 80523, USA.
Nicholas BaezDepartment of Chemistry, Colorado State University, Fort Collins, CO 80523, USA.
George BarisasCell and Molecular Biology Program, Colorado State University, Fort Collins, CO 80523, USA.
Deborah A RoessDepartment of Biomedical Sciences, Colorado State University, Fort Collins, CO 80523, USA.
George R BousfieldDepartment of Biological Sciences, Wichita State University, Wichita, KS 67260, USA.ORCID 0000-0002-5632-7606
Debbie C CransCell and Molecular Biology Program, Colorado State University, Fort Collins, CO 80523, USA.ORCID 0000-0001-7792-3450
Colorado State University · USKing Faisal University · SAWichita State University · US

Funding

NIH HHS NIH AG-029531
6 · The paper itself

Abstract

Signal transduction by luteinizing hormone receptors (LHRs) and follicle-stimulating hormone receptors (FSHRs) is essential for the successful reproduction of human beings. Both receptors and the thyroid-stimulating hormone receptor are members of a subset of G-protein coupled receptors (GPCRs) described as the glycoprotein hormone receptors. Their ligands, follicle-stimulating hormone (FSH) and luteinizing hormone (LH) and a structurally related hormone produced in pregnancy, human chorionic gonadotropin (hCG), are large protein hormones that are extensively glycosylated. Although the primary physiologic functions of these receptors are in ovarian function and maintenance of pregnancy in human females and spermatogenesis in males, there are reports of LHRs or FSHRs involvement in disease processes both in the reproductive system and elsewhere. In this review, we evaluate the aggregation state of the structure of actively signaling LHRs or FSHRs, their functions in reproduction as well as summarizing disease processes related to receptor mutations affecting receptor function or expression in reproductive and non-reproductive tissues. We will also present novel strategies for either increasing or reducing the activity of LHRs signaling. Such approaches to modify signaling by glycoprotein receptors may prove advantageous in treating diseases relating to LHRs or FSHRs function in addition to furthering the identification of new strategies for modulating GPCR signaling.

Indexed as

follicle-stimulating hormone receptorhormonesluteinizing hormone receptor

Identifiers

PMID32942611
PMCPMC7565105
OpenAlexW3085308247

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.