Evidence map›Paper›PMID 30696114›Full record

ReviewInternational journal of molecular sciences2019

GPR68: An Emerging Drug Target in Cancer.

Shu Z Wiley, Krishna Sriram, Cristina Salmerón, Paul A Insel

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
4.1field-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

50 citing papers in PubMed, 95 citations in OpenAlex.

  1. Review
  2. Article
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  6. Article
  7. Article
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  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. GPCRs: emerging targets for novel T cell immune checkpoint therapy.Cancer immunology, immunotherapy : CII · 2024
    Review
  16. Article
  17. Molecular basis of proton-sensing by G protein-coupled receptors.bioRxiv : the preprint server for biology · 2024
    Article
  18. Article
  19. Review
  20. 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

4 authors at 1 institution in 1 country.

Shu Z WileyDepartment of Pharmacology, University of California, San Diego, La Jolla, CA 92093, USA. szwiley@ucsd.edu.
Krishna SriramDepartment of Pharmacology, University of California, San Diego, La Jolla, CA 92093, USA. ksriram@ucsd.edu.
Cristina SalmerónDepartment of Pharmacology, University of California, San Diego, La Jolla, CA 92093, USA. crsalmeronsalvador@ucsd.edu.
Paul A InselDepartment of Pharmacology, University of California, San Diego, La Jolla, CA 92093, USA. pinsel@ucsd.edu.
University of California, San Diego · US

Funding

UCSD Cancer Center Training Program in Drug DevelopmentT32CA121938 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Michael Bouvet, Dwayne G. Stupack · 2006 to 2026
$10.3M
National Institutes of Health CA121938, CA189477NCI NIH HHS T32 CA121938
6 · The paper itself

Abstract

GPR68 (or ovarian cancer G protein-coupled receptor 1, OGR1) is a proton-sensing G-protein-coupled receptor (GPCR) that responds to extracellular acidity and regulates a variety of cellular functions. Acidosis is considered a defining hallmark of the tumor microenvironment (TME). GPR68 expression is highly upregulated in numerous types of cancer. Emerging evidence has revealed that GPR68 may play crucial roles in tumor biology, including tumorigenesis, tumor growth, and metastasis. This review summarizes current knowledge regarding GPR68-its expression, regulation, signaling pathways, physiological roles, and functions it regulates in human cancers (including prostate, colon and pancreatic cancer, melanoma, medulloblastoma, and myelodysplastic syndrome). The findings provide evidence for GPR68 as a potentially novel therapeutic target but in addition, we note challenges in developing drugs that target GPR68.

Indexed as

Molecular Targeted TherapyAnimalsHumansModels, BiologicalNeoplasmsReceptors, G-Protein-CoupledSmall Molecule LibrariesReceptors, G-Protein-CoupledSmall Molecule LibrariesacidosisGPR68proton-sensing GPCRsRNA-seqtumor microenvironment

Identifiers

PMID30696114
PMCPMC6386835
OpenAlexW2913111458

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.