Evidence map›Paper›PMID 33850003›Full record

ArticleMolecular cancer therapeutics2021

Novel TGFβ Inhibitors Ameliorate Oral Squamous Cell Carcinoma Progression and Improve the Antitumor Immune Response of Anti-PD-L1 Immunotherapy.

Nils Ludwig, Łukasz Wieteska, Cynthia S Hinck, Saigopalakrishna S Yerneni, Juliana H Azambuja, Richard J Bauer, Torsten E Reichert, Andrew P Hinck, Theresa L Whiteside

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

18 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
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  6. Targeting collagen to optimize cancer immunotherapy.Experimental hematology & oncology · 2025
    Review
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  8. Article
  9. Article
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  11. Article
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  14. Article
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  16. TGFβJournal of extracellular vesicles · 2022
    Article
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  18. 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

9 authors at 3 institutions in 2 countries.

Nils LudwigDepartment of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania. nils.ludwig@ukr.de whitesidetl@upmc.edu.ORCID 0000-0001-5561-2184
Łukasz WieteskaDepartment of Structural Biology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Cynthia S HinckDepartment of Structural Biology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Saigopalakrishna S YerneniDepartment of Biomedical Engineering, Carnegie Mellon University, Pittsburgh, Pennsylvania.
Juliana H AzambujaDepartment of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Richard J BauerDepartment of Oral and Maxillofacial Surgery, University Hospital Regensburg, Regensburg, Germany.
Torsten E ReichertDepartment of Oral and Maxillofacial Surgery, University Hospital Regensburg, Regensburg, Germany.
Andrew P HinckDepartment of Structural Biology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Theresa L WhitesideDepartment of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania. nils.ludwig@ukr.de whitesidetl@upmc.edu.ORCID 0000-0001-7316-6181
University of Pittsburgh · USUniversity Hospital Regensburg · DECarnegie Mellon University · US

Funding

LIGAND/RECEPTOR INTERACTIONS IN THE TGF BETA SUPERFAMILYR01GM058670 · NIGMS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI HINCK, ANDREW P · 1999 to 2017
$3.6M
Depleting exosomes to improve responses to immune therapy in HNSCCU01DE029759 · NIDCR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WHITESIDE, THERESA L. · 2020 to 2024
$3.5M
Inhibition of the tumor-promoting effects of TGF-beta in advanced prostate cancerR01CA172886 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI HINCK, ANDREW P, SUN, LUZHE · 2013 to 2016
$1.2M
NCI NIH HHS R01 CA172886NIDCR NIH HHS U01 DE029759NIGMS NIH HHS R01 GM058670
6 · The paper itself

Abstract

TGFβ is a key regulator of oral squamous cell carcinoma (OSCC) progression, and its potential role as a therapeutic target has been investigated with a limited success. This study evaluates two novel TGFβ inhibitors as mono or combinatorial therapy with anti-PD-L1 antibodies (α-PD-L1 Ab) in a murine OSCC model. Immunocompetent C57BL/6 mice bearing malignant oral lesions induced by 4-nitroquinoline 1-oxide (4-NQO) were treated for 4 weeks with TGFβ inhibitors mRER (i.p., 50 μg/d) or mmTGFβ2-7m (10 μg/d delivered by osmotic pumps) alone or in combination with α-PD-L1 Abs (7× i.p. of 100 μg/72 h). Tumor progression and body weight were monitored. Levels of bioactive TGFβ in serum were quantified using a TGFβ bioassay. Tissues were analyzed by immunohistology and flow cytometry. Therapy with mRER or mmTGFβ2-7m reduced tumor burden (

Indexed as

AnimalsCarcinoma, Squamous CellDisease ProgressionHumansImmune Checkpoint InhibitorsImmunotherapyLongitudinal StudiesMiceMouth NeoplasmsTransforming Growth Factor betaImmune Checkpoint InhibitorsTransforming Growth Factor beta

Identifiers

PMID33850003
PMCPMC8172434
OpenAlexW3153681565

What OpenQuestion 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 OpenQuestion graph.