Evidence map›Paper›PMID 26756968›Full record

ArticleInternational journal of cancer2016

Treatment to sustain a Th17-type phenotype to prevent skewing toward Treg and to limit premalignant lesion progression to cancer.

M Rita I Young, Corinne A Levingston, Sara D Johnson

Open access · bronzeAbstract read
In one paragraph

Article in International journal of cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

22 citing papers in PubMed, 30 citations in OpenAlex.

  1. Signaling pathways and targeted interventions for precancers.Signal transduction and targeted therapy · 2026
    Review
  2. Article
  3. Article
  4. The Role of IL-17 in the Pathogenesis of Oral Squamous Cell Carcinoma.International journal of molecular sciences · 2023
    Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Interleukin (IL)-12 and IL-23 and Their Conflicting Roles in Cancer.Cold Spring Harbor perspectives in biology · 2018
    Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Th17 Cells in Protection from Tumor or Promotion of Tumor Progression.Journal of clinical & cellular immunology · 2016
    Article
  20. 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

3 authors at 2 institutions in 1 country.

M Rita I YoungResearch Service, Ralph H. Johnson VA Medical Center, Charleston, SC.
Corinne A LevingstonResearch Service, Ralph H. Johnson VA Medical Center, Charleston, SC.
Sara D JohnsonResearch Service, Ralph H. Johnson VA Medical Center, Charleston, SC.
Medical University of South Carolina · USRalph H. Johnson VA Medical Center · US

Funding

Immunotherapy to prevent oral permalignant lesion recurrence and oral cancer.R01CA128837 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI YOUNG, M. RITA · 2009 to 2013
$1.5M
Sustaining a Th17 Phenotype to Prevent Premalignant Lesion Progression to CancerI01CX000851 · VA · RALPH H JOHNSON VA MEDICAL CENTER · PI YOUNG, M. RITA · 2013 to 2016
–
CSRD VA I01 CX000851NCI NIH HHS R01 CA128837NCI NIH HHS R01-CA128837
6 · The paper itself

Abstract

While immune suppression is a hallmark of head and neck squamous cell carcinoma (HSNCC), the immunological impact of premalignant oral lesions, which often precedes development of HNSCC, is unknown. The present study assessed the changes in splenic and draining lymph node CD4(+) cell populations and their production of select cytokines that occur in mice with carcinogen-induced premalignant oral lesions and the changes that occur as lesions progress to oral cancer. These studies found skewing toward Th1 and Th17-type phenotypes in the spleen and lymph nodes of mice with premalignant oral lesions and a shift to Treg as lesions progress to cancer. Since the role of Th17 cells in the progression from premalignant lesions to cancer is not clear, studies determined the immunological and clinical effect of treating mice bearing premalignant oral lesions with a TGF-β type 1 receptor inhibitor plus IL-23 as an approach to sustain the Th17 phenotype. These studies showed that the treatment approach not only sustained the Th17 phenotype, but also increased distal spleen cell and regional lymph node cell production of other stimulatory/inflammatory mediators and slowed premalignant lesion progression to cancer.

Indexed as

AnimalsAntigens, SurfaceBenzamidesBiomarkersCarcinogensCarcinoma, Squamous CellCell Transformation, NeoplasticCytokinesDisease ProgressionFemaleHead and Neck NeoplasmsHumansImmunophenotypingInterleukin-23Lymph NodesMice4-(4-(3-(pyridin-2-yl)-1H-pyrazol-4-yl)pyridin-2-yl)-N-(tetrahydro-2H-pyran-4-yl)benzamideAntigens, SurfaceBenzamidesBiomarkersCarcinogensCytokinesInterleukin-23Pyrazoleshead and neck cancerHNSCCIL-17premalignant oral lesionsTh17Treg

Identifiers

PMID26756968
PMCPMC5925421
OpenAlexW2296584194

What OpenQuestion holds

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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.