Evidence map›Paper›PMID 42595354›Full record

ArticleJournal for immunotherapy of cancer2026

Development of an immunocompetent cutaneous squamous cell carcinoma model identifies VISTA and CTLA-4 as targetable immune checkpoints.

Alanis E Rodriguez Rosario, Roberto Rangel, Nicholas Balbin, Zohra N Nizami, Jaafar Hadi, Ahmed Noor, Liping Dong, Arnoldo Corona, Nikitha Bhavani, Ricardo M Cruz Sanchez and 8 more

Abstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

18 authors.

Alanis E Rodriguez Rosario *University of Puerto Rico School of Medicine, San Juan, Puerto Rico.
Roberto Rangel *Department of Head and Neck Surgery, The University of Texas M.D. Anderson Cancer Center, Houston, TX, USA.
Nicholas BalbinDepartment of Head and Neck Surgery, The University of Texas M.D. Anderson Cancer Center, Houston, TX, USA.
Zohra N NizamiDepartment of Head and Neck Surgery, The University of Texas M.D. Anderson Cancer Center, Houston, TX, USA.
Jaafar HadiDepartment of Head and Neck Surgery, The University of Texas M.D. Anderson Cancer Center, Houston, TX, USA.
Ahmed NoorDepartment of Head and Neck Surgery, The University of Texas M.D. Anderson Cancer Center, Houston, TX, USA.
Liping DongDepartment of Head and Neck Surgery, The University of Texas M.D. Anderson Cancer Center, Houston, TX, USA.
Arnoldo CoronaDepartment of Head and Neck Surgery, The University of Texas M.D. Anderson Cancer Center, Houston, TX, USA.
Nikitha BhavaniDepartment of Head and Neck Surgery, The University of Texas M.D. Anderson Cancer Center, Houston, TX, USA.
Ricardo M Cruz SanchezUniversity of Puerto Rico School of Medicine, San Juan, Puerto Rico.ORCID http://orcid.org/0000-0002-0256-8818
Gemalene M SungaUniversity of Puerto Rico School of Medicine, San Juan, Puerto Rico.
Ratna VeeramachaneniDepartment of Head and Neck Surgery, The University of Texas M.D. Anderson Cancer Center, Houston, TX, USA.
Ganiraju C ManyamDepartment of Bioinformatics and Computational Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Jing WangDepartment of Bioinformatics and Computational Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Wendong YuDepartment of Pathology Anatomical, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Andrew G SikoraDepartment of Head and Neck Surgery, The University of Texas M.D. Anderson Cancer Center, Houston, TX, USA agsikora@mdanderson.org jmyers@mdanderson.org rrangel@mdanderson.org.
Jeffrey N MyersDepartment of Head and Neck Surgery, The University of Texas M.D. Anderson Cancer Center, Houston, TX, USA agsikora@mdanderson.org jmyers@mdanderson.org rrangel@mdanderson.org.
Roberto RangelDepartment of Head and Neck Surgery, The University of Texas M.D. Anderson Cancer Center, Houston, TX, USA agsikora@mdanderson.org jmyers@mdanderson.org rrangel@mdanderson.org.

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI DIANE BODURKA · 1985 to 2026
$290.8M
Targeting the immunosuppressive tumor microenvironment to enhance efficacy of radiotherapy and immuno-radiotherapy for oral cancerU01DE028233 · NIDCR · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI ANNAPRAGADA, ANANTH V, SIKORA, ANDREW · 2018 to 2022
$3.9M
Functional roles of GOF TP53 mutations in metastasis and immunosuppression of head and neck cancersR01DE030875 · NIDCR · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Jeffrey Nicholas Myers, Andrew Sikora · 2022 to 2026
$2.8M
UPWARDS Training Program (Underrepresented Minorities Working Towards Research Diversity in Science)R25CA240137 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KEYOMARSI, KHANDAN, WATOWICH, STEPHANIE S · 2020 to 2024
$2.1M
NCI NIH HHS P30 CA016672NCI NIH HHS R25 CA240137NIDCR NIH HHS R01 DE030875NIDCR NIH HHS U01 DE028233
6 · The paper itself

Abstract

backgroundImmunotherapeutic approaches for cutaneous squamous cell carcinoma (cSCC) remain limited to programmed cell death protein 1 (PD-1) blockade. Although genomics studies have characterized key driver mutations in cSCC, preclinical models that faithfully recapitulate both the genetic landscape and immune microenvironment of the human disease, that could drive the development of novel, effective therapies, are lacking.

methodsTo address this need, we generated genetically engineered mouse models harboring inducible

resultsWhole exome sequencing confirmed alterations overlapping with human cSCC, including mutations in

conclusionsThese results establish a robust, genetically defined, immunocompetent platform for modeling cSCC and evaluating novel immunotherapeutic strategies for treating patients with this disease. Our findings also identify VISTA and CTLA-4 as promising immune checkpoints to target in cSCC and support clinical evaluation of this combination of immune checkpoint blockade to overcome immune checkpoint inhibitor resistance and improve clinical outcomes.

Indexed as

CTLA-4 AntigenCutaneous Squamous Cell CarcinomaImmune Checkpoint InhibitorsSkin NeoplasmsAnimalsDisease Models, AnimalFemaleHumansMiceCTLA-4 AntigenImmune Checkpoint InhibitorsImmune Checkpoint InhibitorImmunosuppressionImmunotherapySkin Cancer

Identifiers

PMID42595354
PMCPMC13475135

What OpenQuestion holds

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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 OpenQuestion graph.