Evidence map›Paper›PMID 41331220›Full record

ArticleDiscover oncology2025

Expression and functional diversity of the glucagon-like peptide-1 receptor across tumor types.

Mario M Alba, Wilson H Lee, Jerry S H Lee, Zhipeng Lu, Bangyan Stiles, Hagai Ligumsky

Abstract read
In one paragraph

Article in Discover oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Mario M Alba *Department of Pharmacology and Pharmaceutical Sciences, Alfred E. Mann School of Pharmacy, University of Southern California, Los Angeles, CA, USA.
Wilson H Lee *Department of Pharmacology and Pharmaceutical Sciences, Alfred E. Mann School of Pharmacy, University of Southern California, Los Angeles, CA, USA.
Jerry S H LeeEllison Medical Institute, Los Angeles, CA, USA.
Zhipeng LuDepartment of Pharmacology and Pharmaceutical Sciences, Alfred E. Mann School of Pharmacy, University of Southern California, Los Angeles, CA, USA.
Bangyan StilesDepartment of Pharmacology and Pharmaceutical Sciences, Alfred E. Mann School of Pharmacy, University of Southern California, Los Angeles, CA, USA.
Hagai LigumskyEllison Medical Institute, Los Angeles, CA, USA. hligumsky@emila.org.ORCID http://orcid.org/0000-0002-5652-3703

Funding

Decoding global RNP topologies in splicing regulationR01HG012928 · NHGRI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Zhipeng Lu · 2023 to 2026
$2.2M
High Throughput Determination of RNA 3D Structures and Dynamics in VivoR35GM143068 · NIGMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI LU, ZHIPENG · 2021 to 2025
$2.1M
The Role of ERRa in liver lipid dysfunction and pathologyR01DK131492 · NIDDK · UNIVERSITY OF SOUTHERN CALIFORNIA · PI STILES, BANGYAN · 2022 to 2025
$1.5M
Hepatic Steatosis Induced by Bioactive LipidsF31DK138790 · NIDDK · UNIVERSITY OF SOUTHERN CALIFORNIA · PI ALBA, MARIO · 2024 to 2024
$31k
NHGRI NIH HHS R01 HG012928NIDDK NIH HHS F31 DK138790NIDDK NIH HHS R01 DK131492NIGMS NIH HHS R35 GM143068NIH HHS F31DK138790-01NIH HHS R01DK131492NIH HHS R01HG012928NIH HHS R35GM143068
6 · The paper itself

Abstract

purposeGlucagon-like peptide-1 receptor (GLP-1R) agonists are widely used to treat type 2 diabetes mellitus (T2DM) and obesity. Emerging evidence suggests potential links between GLP-1R signaling and cancer risk or progression, but its role in tumor biology remains unclear. This study investigated GLP-1R expression and prognostic value across multiple cancer types using large-scale genomic datasets.

methodsWe analyzed GLP-1R mRNA expression using data from The Cancer Genome Atlas (TCGA), Genotype-Tissue Expression (GTEx), and the Human Protein Atlas. Expression patterns in tumors were compared to normal tissues, including samples from rapid autopsies. Survival analyses were conducted across cancer types, and GLP-1R gene alterations were assessed via cBioPortal.

resultsGLP-1R expression showed marked variation across cancers. It was lower in breast, lung, and colon cancers, but elevated in esophageal, kidney, and thyroid tumors compared to normal tissues. Higher GLP-1R expression correlated with improved overall survival in low-grade glioma but with worse outcomes in lung squamous cell carcinoma. Patterns of disease-free survival varied similarly. Genetic alterations in GLP-1R were rare, with amplifications most common, particularly in esophageal and ovarian cancers.

conclusionGLP-1R shows tissue-specific expression and prognostic relevance across cancer types. The low expression of GLP-1R across cancer types and the low frequency of genetic alterations suggest a limited direct role of GLP-1R mutations in cancer progression, but its variable expression may influence tumor behavior. Further research is needed to clarify both the functional role of GLP-1R in cancer biology and the safety and therapeutic potential of GLP-1R agonists in oncology.

Indexed as

GLP-1R agonistsmRNA expressionPancancerPrognosis

Identifiers

PMID41331220
PMCPMC12779865

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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Registered trials

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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.