Evidence map›Paper›PMID 41190345›Full record

ReviewFrontiers in aging2025

Acid sensing to inflammaging: mechanisms and therapeutic promise of GPR68 (OGR1) in aging-related diseases.

Jianlei Wei, Fengxin Cui, Zhihua Huang, Zeping Li, Zebin Mao, Pengxia Zhang

Abstract readReview
In one paragraph

Review in Frontiers in aging, 2025. 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
–field-weighted citation impact
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.

  1. Article
  2. Review
  3. Review
  4. Review
  5. 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

6 authors.

Jianlei WeiSchool of Basic Medicine, Jiamusi University, Jiamusi, Heilongjiang, China.
Fengxin CuiThe Seventh People's Hospital affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Zhihua HuangDepartment of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Peking University, Beijing, China.
Zeping LiDepartment of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Peking University, Beijing, China.
Zebin MaoDepartment of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Peking University, Beijing, China.
Pengxia ZhangSchool of Basic Medicine, Jiamusi University, Jiamusi, Heilongjiang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

GPR68 is a proton-sensing G protein-coupled receptor with an activation threshold at extracellular pH values between 6.5 and 7.0. It is widely expressed in diverse cell types, particularly in fibroblasts and cancer cells, within inflammatory and tumor microenvironments. In inflammatory bowel disease patients, GPR68 expression is also significantly increased in macrophages and monocytes. GPR68 primarily modulates inflammatory responses through the Gq/11-phospholipase C-inositol 1,4,5-trisphosphate/Ca

Indexed as

aging-related diseaseschronic inflammationGPR68immune responsetherapeutic target

Identifiers

PMID41190345
PMCPMC12580631

What OpenQuestion holds

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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.