Evidence map›Paper›PMID 32301180›Full record

ReviewMolecular carcinogenesis2020

The role of transforming growth factor-beta in immune suppression and chronic inflammation of squamous cell carcinomas.

Alexander A Strait, Xiao-Jing Wang

Open access · greenAbstract readReview
In one paragraph

Review in Molecular carcinogenesis, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

12 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Leukoplakia and Immunology: New Chemoprevention Landscapes?International journal of molecular sciences · 2020
    Review
  12. Article
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

2 authors at 2 institutions in 1 country.

Alexander A StraitDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, Colorado.ORCID 0000-0003-2397-8311
Xiao-Jing WangDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, Colorado.ORCID 0000-0001-8695-7361
University of Colorado Anschutz Medical Campus · USVA Eastern Colorado Health Care System · US

Funding

PREDOCTORAL TRAINING PROGRAM IN PHARMACOLOGYT32GM007635 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI DELL'ACQUA, MARK L · 1985 to 2023
$6.1M
Training in Translational Research of Skin DiseasesT32AR007411 · NIAMS · UNIVERSITY OF COLORADO DENVER · PI ASGARI, MARYAM MANDANA, ROOP, DENNIS · 1986 to 2025
$4.8M
Training in Translational Research of Lung, Head and Neck CancerT32CA174648 · NCI · UNIVERSITY OF COLORADO DENVER · PI KARAM, SANA D · 2013 to 2022
$4.2M
Role of TGFbeta signaling in HNSCC progressionR01DE015953 · NIDCR · UNIVERSITY OF COLORADO DENVER · PI WANG, XIAO-JING · 2004 to 2014
$3.6M
Elucidating Mechanism of Immune Evasion in Head and Neck CancersR01DE027329 · NIDCR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WANG, JING HONG, WANG, XIAO-JING · 2018 to 2022
$2.8M
ROLE OF SMADS IN THE EPIDERMIS AND SKIN CARCINOGENESISR01CA087849 · NCI · UNIVERSITY OF COLORADO DENVER · PI WANG, XIAO-JING · 2000 to 2011
$2.7M
Mechanisms of Dual Inhibition of TGFbeta/PD-L1 in HNSCCR01DE028420 · NIDCR · UNIVERSITY OF COLORADO DENVER · PI WANG, JING HONG, WANG, XIAO-JING · 2019 to 2023
$2.7M
Identifying oral cancer stem cell properties affected by the microenvironmentR01DE024371 · NIDCR · UNIVERSITY OF COLORADO DENVER · PI JIMENO, ANTONIO, WANG, XIAO-JING · 2014 to 2017
$2.1M
TGF BETA SIGNALING AND SKIN CARCINOGENESISR01CA079998 · NCI · UNIVERSITY OF COLORADO DENVER · PI WANG, XIAO-JING · 1999 to 2009
$2.1M
Mechanisms of Breaking Indolence in Squamous Cell CarcinomaI01BX003232 · VA · VA NORTHERN CALIFORNIA HEALTH CARE SYS · PI WANG, XIAO-JING · 2017 to 2025
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BLRD VA I01 BX003232NCI NIH HHS R01 CA079998NCI NIH HHS R01 CA087849NCI NIH HHS T32 CA174648NIAMS NIH HHS T32 AR007411NIDCR NIH HHS R01 DE015953NIDCR NIH HHS R01 DE024371NIDCR NIH HHS R01 DE027329NIDCR NIH HHS R01 DE028420NIGMS NIH HHS T32 GM007635
6 · The paper itself

Abstract

Despite a decline in the incidence of squamous cell carcinomas (SCCs) over the past 20 years, their survival rate has remained nearly the same, indicating that treatment options have not improved relative to other cancer types. Immunotherapies have a high potential for a sustained effect in SCC patients, but their response rate is low. Here, we review the suppressive role of transforming growth factor-beta (TGFβ) on the antitumor immune response in SCC and present its potential as a therapeutic target in combination with the current range of immunotherapies available for SCC patients. We conclude that SCCs are an optimal cancer type to study the effectiveness of TGFβ inhibition due to the prevalence of dysregulated TGFβ signaling in them.

Indexed as

AnimalsCarcinoma, Squamous CellHumansImmunotherapyInflammationSignal TransductionTransforming Growth Factor betaTransforming Growth Factor betahead and neck squamous cell carcinomaimmune checkpoint blockadeimmunotherapytumor microenvironment

Identifiers

PMID32301180
PMCPMC7282943
OpenAlexW3016680872

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.