Evidence map›Paper›PMID 37350933›Full record

ArticleFrontiers in oncology2023

G protein-coupled receptor GPR68 inhibits lymphocyte infiltration and contributes to gender-dependent melanoma growth.

Shangmei Ye, Yunfeng Zhu, Dongmei Zhong, Xiaodong Song, Jialin Li, Fang Xiao, Zhilei Huang, Wenjie Zhang, Mingyue Wu, Kangdi Zhang and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. GPCRs: emerging targets for novel T cell immune checkpoint therapy.Cancer immunology, immunotherapy : CII · 2024
    Review
  6. Review
  7. Recent advances in acid sensing by G protein coupled receptors.Pflugers Archiv : European journal of physiology · 2024
    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

12 authors at 2 institutions in 1 country.

Shangmei YeInstitute of Precision Medicine, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Yunfeng ZhuInstitute of Precision Medicine, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Dongmei ZhongInstitute of Precision Medicine, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Xiaodong SongDepartment of Critical Care Medicine, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Jialin LiDepartment of Critical Care Medicine, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Fang XiaoDepartment of Critical Care Medicine, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Zhilei HuangInstitute of Precision Medicine, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Wenjie ZhangInstitute of Precision Medicine, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Mingyue WuInstitute of Precision Medicine, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Kangdi ZhangInstitute of Precision Medicine, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Fu-Li XiangInstitute of Precision Medicine, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Jie XuInstitute of Precision Medicine, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Sun Yat-sen University · CNThe First Affiliated Hospital, Sun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Melanoma is a common and aggressive type of skin cancer with rising incidence rate globally. Gender is one of the determining factors, and overall males have a higher risk of developing melanoma as well as worse prognosis. Emerging evidence show that GPR68, a G protein-coupled receptor that is sensitive to acid and mechanical stimulations for cellular microenvironment, plays an important role in tumor biology. However, whether GPR68 is involved in gender-dependent regulation of tumor growth is unclear. Methods: We established a syngeneic melanoma model in Results: GPR68 is required for melanoma growth in males but dispensable in females. GPR68 is expressed and functional in B16-F10 melanocytes, but the activity of the receptor does not directly contribute to proliferation and migration of the cells. GPR68 inhibits infiltration of CD45 Discussion: GPR68 is sensor for acid and mechanical stimulations, which are two important factors in the microenvironment associated with tumor growth and metastasis. Our results suggest a prominent role of the receptor molecules in tumor biology in a gender-dependent manner. Since GPCRs are more feasible to develop small molecule drugs compared to transcription factors, our study demonstrates the potential of GPR68 as a novel druggable therapeutic target for melanoma in male patients.

Indexed as

gender dependenceGPR68infiltrationmelanomaNK cellsT cells

Identifiers

PMID37350933
PMCPMC10282648
OpenAlexW4379798090

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.