Evidence map›Paper›PMID 39423285›Full record

ArticleScience immunology2024

The acid-sensing receptor GPR65 on tumor macrophages drives tumor growth in obesity.

Sreya Bagchi, Robert Yuan, Han-Li Huang, Weiruo Zhang, David Kung-Chun Chiu, Hyungjoo Kim, Sophia L Cha, Lorna Tolentino, Joshua Lowitz, Yilin Liu and 4 more

Abstract read
In one paragraph

Article in Science immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Review
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  5. Mechanical interplay between adipose tissues and disease progression.Bioengineering & translational medicine · 2026
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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

14 authors.

Sreya BagchiDepartment of Pathology, Stanford University, Stanford, CA 94305, USA.ORCID 0009-0009-9471-3557
Robert YuanDepartment of Pathology, Stanford University, Stanford, CA 94305, USA.
Han-Li HuangDepartment of Pathology, Stanford University, Stanford, CA 94305, USA.ORCID 0000-0001-8515-1219
Weiruo ZhangDepartment of Biological Data Science, Stanford University, Stanford, CA 94305, USA.ORCID 0000-0003-3680-7562
David Kung-Chun ChiuDepartment of Pathology, Stanford University, Stanford, CA 94305, USA.
Hyungjoo KimDepartment of Pathology, Stanford University, Stanford, CA 94305, USA.ORCID 0000-0003-1627-4797
Sophia L ChaDepartment of Pathology, Stanford University, Stanford, CA 94305, USA.ORCID 0000-0002-5344-900X
Lorna TolentinoDepartment of Pathology, Stanford University, Stanford, CA 94305, USA.
Joshua LowitzAntibody Solutions, Santa Clara, CA 95054, USA.ORCID 0009-0008-7142-3752
Yilin LiuDepartment of Pathology, Stanford University, Stanford, CA 94305, USA.
Anna MoshnikovaPhysics Department, University of Rhode Island, Kingston, RI 02881, USA.ORCID 0000-0002-4431-1551
Oleg AndreevPhysics Department, University of Rhode Island, Kingston, RI 02881, USA.ORCID 0000-0001-7086-0055
Sylvia PlevritisDepartment of Biological Data Science, Stanford University, Stanford, CA 94305, USA.ORCID 0000-0002-4155-5542
Edgar G EnglemanDepartment of Pathology, Stanford University, Stanford, CA 94305, USA.ORCID 0000-0002-2096-9279

Funding

Systems Biology of Tumor-Immune-Stromal Interactions in Metastatic ProgressionU54CA274511 · NCI · STANFORD UNIVERSITY · PI JOSEPH B SHRAGER · 2023 to 2026
$9.5M
Innate Immune Mechanisms Contributing to Cancer Growth in ObesityR01CA262361 · NCI · STANFORD UNIVERSITY · PI ENGLEMAN, EDGAR G. · 2021 to 2025
$2.9M
Effects of Maternal Obesity on Offspring Immune SystemR21HD098688 · NICHD · STANFORD UNIVERSITY · PI ENGLEMAN, EDGAR G. · 2019 to 2020
$438k
NCI NIH HHS R01 CA262361NCI NIH HHS U54 CA274511NICHD NIH HHS R21 HD098688
6 · The paper itself

Abstract

Multiple cancers, including colorectal cancer (CRC), are more frequent and often more aggressive in individuals with obesity. Here, we showed that macrophages accumulated within tumors of patients with obesity and CRC and in obese CRC mice and that they promoted accelerated tumor growth. These changes were initiated by oleic acid accumulation and subsequent tumor cell-derived acid production and were driven by macrophage signaling through the acid-sensing receptor GPR65. We found a similar role for GPR65 in hepatocellular carcinoma (HCC) in obese mice. Tumors in patients with obesity and CRC or HCC also exhibited increased GPR65 expression, suggesting that the mechanism revealed here may contribute to tumor growth in a range of obesity-associated cancers and represent a potential therapeutic target.

Indexed as

Liver NeoplasmsObesityReceptors, G-Protein-CoupledAnimalsCarcinoma, HepatocellularColorectal NeoplasmsFemaleHumansMacrophagesMaleMiceMice, Inbred C57BLMice, KnockoutMice, ObeseTumor-Associated MacrophagesGPR65 protein, mouseReceptors, G-Protein-Coupled

Identifiers

PMID39423285
PMCPMC12104511

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.