Evidence map›Paper›PMID 31804466›Full record

ArticleNature communications2019

Syngeneic animal models of tobacco-associated oral cancer reveal the activity of in situ anti-CTLA-4.

Zhiyong Wang, Victoria H Wu, Michael M Allevato, Mara Gilardi, Yudou He, Juan Luis Callejas-Valera, Lynn Vitale-Cross, Daniel Martin, Panomwat Amornphimoltham, James Mcdermott and 9 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 108 papers.

0numbers the graph read from it
0cells of the map it votes in
108citing papers in PubMed
7.6field-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

108 citing papers in PubMed, 166 citations in OpenAlex.

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48 more citing papers are in PubMed but not listed here.

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

19 authors at 7 institutions in 4 countries.

Zhiyong WangMoores Cancer Center, University of California San Diego, 3855 Health Sciences Drive, La Jolla, CA, USA.ORCID http://orcid.org/0000-0002-3574-6078
Victoria H WuMoores Cancer Center, University of California San Diego, 3855 Health Sciences Drive, La Jolla, CA, USA.
Michael M AllevatoMoores Cancer Center, University of California San Diego, 3855 Health Sciences Drive, La Jolla, CA, USA.
Mara GilardiMoores Cancer Center, University of California San Diego, 3855 Health Sciences Drive, La Jolla, CA, USA.
Yudou HeDepartment of Cellular and Molecular Medicine, University of California San Diego, La Jolla, CA, USA.ORCID http://orcid.org/0000-0001-8733-8781
Juan Luis Callejas-ValeraCancer Biology and Immunotherapies Group, Sanford Research, Sioux Falls, SD, USA.ORCID http://orcid.org/0000-0002-5614-6370
Lynn Vitale-CrossNational Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD, USA.
Daniel MartinNational Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD, USA.
Panomwat AmornphimolthamInternational College of Dentistry, Walailak University, Nakhon Si Thammarat, Thailand.
James McdermottMoores Cancer Center, University of California San Diego, 3855 Health Sciences Drive, La Jolla, CA, USA.
Bryan S YungMoores Cancer Center, University of California San Diego, 3855 Health Sciences Drive, La Jolla, CA, USA.
Yusuke GotoMoores Cancer Center, University of California San Diego, 3855 Health Sciences Drive, La Jolla, CA, USA.
Alfredo A MolinoloMoores Cancer Center, University of California San Diego, 3855 Health Sciences Drive, La Jolla, CA, USA.
Andrew B SharabiMoores Cancer Center, University of California San Diego, 3855 Health Sciences Drive, La Jolla, CA, USA.
Ezra E W CohenMoores Cancer Center, University of California San Diego, 3855 Health Sciences Drive, La Jolla, CA, USA.
Qianming ChenState Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
J Guy LyonsDermatology, Bosch Institute, University of Sydney, Camperdown, NSW, 2050, Australia.ORCID http://orcid.org/0000-0002-4835-4663
Ludmil B AlexandrovMoores Cancer Center, University of California San Diego, 3855 Health Sciences Drive, La Jolla, CA, USA.ORCID http://orcid.org/0000-0003-3596-4515
J Silvio GutkindMoores Cancer Center, University of California San Diego, 3855 Health Sciences Drive, La Jolla, CA, USA. sgutkind@ucsd.edu.ORCID http://orcid.org/0000-0002-5150-4482
University of California San Diego · USNational Institutes of Health · USSanford Research · USSichuan University · CNThe University of Sydney · AUUC San Diego Health System · USWalailak University · TH

Funding

VIRAL MALIGNANCYP30CA023100 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI DIANE M SIMEONE · 1985 to 2026
$124.9M
GRADUATE TRAINING IN CELLULAR &MOLECULAR PHARMACOLOGYT32GM007752 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI BROWN, JOAN HELLER, HANDEL, TRACY M · 1985 to 2023
$13.5M
Predoctoral and Postdoctoral Training in Cancer Cell BiologyT32CA067754 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI JEAN Y.J. WANG · 1995 to 2026
$6.5M
Targeting Signaling Vulnerabilities for Oral Cancer PreventionR01DE026644 · NIDCR · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Jorge Silvio Gutkind, SCOTT M LIPPMAN · 2017 to 2026
$4.7M
Stimulating Neo-Antigen Specific T Cell Responses in Head and Neck CancersU01DE028227 · NIDCR · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI GUTKIND, JORGE SILVIO, RAO, ANJANA · 2018 to 2022
$4.6M
Targeting the EGFR-PI3K/mTOR Signaling Circuitry: A Network-Based Approach for Oral Cancer Precision TherapyR01DE026870 · NIDCR · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GUTKIND, JORGE SILVIO · 2018 to 2022
$2.3M
Super-resolution confocal microscopeS10OD021831 · OD · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI LEY, KLAUS F. · 2017 to 2017
$566k
NCI NIH HHS P30 CA023100NCI NIH HHS T32 CA067754NIDCR NIH HHS R01 DE026644NIDCR NIH HHS R01 DE026870NIDCR NIH HHS U01 DE028227NIGMS NIH HHS T32 GM007752NIH HHS S10 OD021831
6 · The paper itself

Abstract

Head and neck squamous cell carcinoma (HNSCC) is the sixth most common cancer worldwide. Tobacco use is the main risk factor for HNSCC, and tobacco-associated HNSCCs have poor prognosis and response to available treatments. Recently approved anti-PD-1 immune checkpoint inhibitors showed limited activity (≤20%) in HNSCC, highlighting the need to identify new therapeutic options. For this, mouse models that accurately mimic the complexity of the HNSCC mutational landscape and tumor immune environment are urgently needed. Here, we report a mouse HNSCC model system that recapitulates the human tobacco-related HNSCC mutanome, in which tumors grow when implanted in the tongue of immunocompetent mice. These HNSCC lesions have similar immune infiltration and response rates to anti-PD-1 (≤20%) immunotherapy as human HNSCCs. Remarkably, we find that >70% of HNSCC lesions respond to intratumoral anti-CTLA-4. This syngeneic HNSCC mouse model provides a platform to accelerate the development of immunotherapeutic options for HNSCC.

Indexed as

AnimalsAntineoplastic Agents, ImmunologicalCarcinoma, Squamous CellCell Line, TumorDisease Models, AnimalHead and Neck NeoplasmsHumansImmunotherapyIpilimumabMiceMouth NeoplasmsAntineoplastic Agents, ImmunologicalIpilimumab

Identifiers

PMID31804466
PMCPMC6895221
OpenAlexW2994508410

What OpenQuestion holds

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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.