Evidence map›Paper›PMID 22408746›Full record

ArticleCancer discovery2011

TGF-β receptor II loss promotes mammary carcinoma progression by Th17 dependent mechanisms.

Sergey V Novitskiy, Michael W Pickup, Agnieszka E Gorska, Philip Owens, Anna Chytil, Mary Aakre, Huiyun Wu, Yu Shyr, Harold L Moses

Abstract read
In one paragraph

Article in Cancer discovery, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 90 papers.

0numbers the graph read from it
0cells of the map it votes in
90citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

90 citing papers in PubMed, 130 citations in OpenAlex.

  1. Article
  2. Review
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  6. Article
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  8. Article
  9. Review
  10. Review
  11. Review
  12. The IL-17 family in diseases: from bench to bedside.Signal transduction and targeted therapy · 2023
    Review
  13. Review
  14. Review
  15. Article
  16. Innate Immunity in Cancer Biology and Therapy.International journal of molecular sciences · 2023
    Review
  17. Review
  18. Review
  19. Review
  20. Circulating Histones to Detect and Monitor the Progression of Cancer.International journal of molecular sciences · 2023
    Review

30 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

9 authors at 1 institution in 1 country.

Sergey V NovitskiyDepartment of Cancer Biology, Vanderbilt University, Nashville, TN 37212, USA.
Michael W Pickup
Agnieszka E Gorska
Philip Owens
Anna Chytil
Mary Aakre
Huiyun Wu
Yu Shyr
Harold L Moses
Vanderbilt University · US

Funding

Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI MATTHEW J TYSKA · 1995 to 2026
$172.8M
TrainingU54CA163072 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Karen Marie Winkfield · 2011 to 2026
$20.1M
Protein Collection and Proteomics Integrative Shared ResourceU54CA126505 · NCI · VANDERBILT UNIVERSITY · PI MOSES, HAROLD L · 2006 to 2010
$8.2M
TGF BETA SUPPRESSION AND PROMOTION OF MAMMARY CARCINOMASR01CA085492 · NCI · VANDERBILT UNIVERSITY · PI MOSES, HAROLD L, WEAVER, VALERIE MARIE · 2000 to 2015
$6.4M
TGF-beta in Mammary Development and TumorigenesisR01CA102162 · NCI · VANDERBILT UNIVERSITY · PI MOSES, HAROLD L · 2003 to 2013
$4.5M
BLRD VA IK6 BX005225NCI NIH HHS CA068485NCI NIH HHS CA085492NCI NIH HHS CA126505NCI NIH HHS P30 CA068485NCI NIH HHS R01 CA085492NCI NIH HHS R01 CA102162NCI NIH HHS U54 CA126505NCI NIH HHS U54 CA163072PHS HHS A102162
6 · The paper itself

Abstract

We report that IL-17 significantly increases the secretion of CXCL1 and CXCL5 from mammary carcinoma cells, which is downregulated by TGF-β through the type II TGF-β receptor (TβRII). Carcinoma cells with conditional knockout of TβRII (Tgfbr2(KO)) have enhanced sensitivity to IL-17a in the stimulation of chemokine secretion. During polyoma middle T (PyMT) induced tumor progression, levels of Th17 inducing cytokines TGF-β, IL-6, IL-23 were increased in PyMT/Tgfbr2(KO) tumors, which was associated with an increased number of Th17 cells. IL-17 increased the suppressive function of MDSCs on T cells through the upregulation of Arg, IDO, and COX2. Treatment of PyMT/Tgfbr2(KO) mice with anti-IL-17 Ab decreased carcinoma growth and metastatic burden. Analysis of human breast cancer transcriptome databases showed a strong association between IL-17 gene expression and poor outcome in lymph node positive, estrogen receptor negative or luminal B subtypes suggesting potential therapeutic approaches.

Indexed as

alpha-FetoproteinsAnimalsBreast NeoplasmsCell Line, TumorChemokines, CXCCyclooxygenase 2Disease ProgressionFemaleGene Expression Regulation, NeoplasticHumansInterleukin-17LigandsMammary Neoplasms, ExperimentalMiceMice, Inbred C57BLMice, Knockoutalpha-fetoprotein related protein, mousealpha-FetoproteinsChemokines, CXCCyclooxygenase 2Interleukin-17LigandsProtein Serine-Threonine KinasesReceptors, Transforming Growth Factor betaReceptor, Transforming Growth Factor-beta Type II

Identifiers

PMID22408746
PMCPMC3297196
OpenAlexW2131506441

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.