Evidence map›Paper›PMID 31710313›Full record

ArticleThe Journal of clinical investigation2019

Galectin-1-driven T cell exclusion in the tumor endothelium promotes immunotherapy resistance.

Dhanya K Nambiar, Todd Aguilera, Hongbin Cao, Shirley Kwok, Christina Kong, Joshua Bloomstein, Zemin Wang, Vangipuram S Rangan, Dadi Jiang, Rie von Eyben and 9 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 109 papers.

0numbers the graph read from it
0cells of the map it votes in
109citing papers in PubMed
6.6field-weighted citation impact, top 2% 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

109 citing papers in PubMed, 166 citations in OpenAlex.

  1. Circulating galectin-1 delineates response to bevacizumab in melanoma patients and reprograms endothelial cell biology.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Trial
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  9. NK Cell Activation by Platinum Boosts Immunotherapy in HRAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
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49 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 6 institutions in 1 country.

Dhanya K NambiarDepartment of Radiation Oncology, Stanford University School of Medicine, Stanford, California, USA.
Todd AguileraDepartment of Radiation Oncology, University of Texas Southwestern, Dallas, Texas, USA.
Hongbin CaoDepartment of Radiation Oncology, Stanford University School of Medicine, Stanford, California, USA.
Shirley KwokDepartment of Pathology, Stanford University School of Medicine, Stanford, California, USA.
Christina KongDepartment of Pathology, Stanford University School of Medicine, Stanford, California, USA.
Joshua BloomsteinDepartment of Radiation Oncology, Stanford University School of Medicine, Stanford, California, USA.
Zemin WangBiologics Discovery California, Bristol-Myers Squibb, Redwood City, California, USA.
Vangipuram S RanganBiologics Discovery California, Bristol-Myers Squibb, Redwood City, California, USA.
Dadi JiangDepartment of Radiation Oncology, University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Rie von EybenDepartment of Radiation Oncology, Stanford University School of Medicine, Stanford, California, USA.
Rachel LiangDepartment of Radiation Oncology, Stanford University School of Medicine, Stanford, California, USA.
Sonya AgarwalDepartment of Radiation Oncology, Stanford University School of Medicine, Stanford, California, USA.
A Dimitrios ColevasDepartment of Medicine, Stanford University School of Medicine, Stanford, California, USA.
Alan KormanBiologics Discovery California, Bristol-Myers Squibb, Redwood City, California, USA.
Clint T AllenTranslational Tumor Immunology Program, National Institute on Deafness and Other Communication Disorders (NIDCD), Bethesda, Maryland, USA.
Ravindra UppaluriDepartment of Surgery - Otolaryngology, Brigham and Women's Hospital and Dana-Farber Cancer Institute, Boston, Massachusetts, USA.
Albert C KoongDepartment of Radiation Oncology, University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Amato GiacciaDepartment of Radiation Oncology, Stanford University School of Medicine, Stanford, California, USA.
Quynh Thu LeDepartment of Radiation Oncology, Stanford University School of Medicine, Stanford, California, USA.
Stanford University · USBristol-Myers Squibb (United States) · USThe University of Texas MD Anderson Cancer Center · USDana-Farber Brigham Cancer Center · USNational Institute on Deafness and Other Communication Disorders · USThe University of Texas Southwestern Medical Center · US

Funding

Translational Oncology Research Program (Project-005)P30CA124435 · NCI · STANFORD UNIVERSITY · PI Melinda L. Telli · 2007 to 2026
$71.4M
TUMOR HYPOXIA--MOLECULAR STUDIES &CLINICAL EXPLOITATIONP01CA067166 · NCI · STANFORD UNIVERSITY · PI LE, QUYNH-THU XUAN · 1996 to 2017
$25.5M
The Impact of Mitochondrial Repression and Lipid Accumulation by HIF on Tumor GrowthR35CA197713 · NCI · STANFORD UNIVERSITY · PI GIACCIA, AMATO J. · 2015 to 2021
$5.3M
Targeting Galectin-1 with radiation in lung cancerR01CA161585 · NCI · STANFORD UNIVERSITY · PI KOONG, ALBERT, LE, QUYNH-THU XUAN · 2012 to 2016
$1.6M
Cancer Research UK 28736Medical Research Council MC_UU_00001/8NCI NIH HHS P01 CA067166NCI NIH HHS P30 CA124435NCI NIH HHS R01 CA161585NCI NIH HHS R35 CA197713
6 · The paper itself

Abstract

Immune checkpoint inhibitors (ICIs), although promising, have variable benefit in head and neck cancer (HNC). We noted that tumor galectin-1 (Gal1) levels were inversely correlated with treatment response and survival in patients with HNC who were treated with ICIs. Using multiple HNC mouse models, we show that tumor-secreted Gal1 mediates immune evasion by preventing T cell migration into the tumor. Mechanistically, Gal1 reprograms the tumor endothelium to upregulate cell-surface programmed death ligand 1 (PD-L1) and galectin-9. Using genetic and pharmacological approaches, we show that Gal1 blockade increases intratumoral T cell infiltration, leading to a better response to anti-PD1 therapy with or without radiotherapy. Our study reveals the function of Gal1 in transforming the tumor endothelium into an immune-suppressive barrier and that its inhibition synergizes with ICIs.

Indexed as

AdultAgedAged, 80 and overAnimalsB7-H1 AntigenEndotheliumFemaleGalectin 1GalectinsHead and Neck NeoplasmsHumansImmune ToleranceImmunotherapyMaleMiceMice, Inbred C57BLB7-H1 AntigenGalectin 1GalectinsLGALS9 protein, humanProgrammed Cell Death 1 ReceptorSTAT1 protein, humanSTAT1 Transcription FactorHead and neck cancerImmunotherapyOncologyRadiation therapy

Identifiers

PMID31710313
PMCPMC6877340
OpenAlexW2983070298

What OpenQuestion holds

Textmetadata
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.