Evidence map›Paper›PMID 26851186›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2016

STAT3/5-Dependent IL9 Overexpression Contributes to Neoplastic Cell Survival in Mycosis Fungoides.

Pablo A Vieyra-Garcia, Tianling Wei, David Gram Naym, Simon Fredholm, Regina Fink-Puches, Lorenzo Cerroni, Niels Odum, John T O'Malley, Robert Gniadecki, Peter Wolf

Open access · bronzeAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
6.7field-weighted citation impact, top 3% 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

30 citing papers in PubMed, 47 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. "Next top" mouse models advancing CTCL research.Frontiers in cell and developmental biology · 2024
    Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Solar UVR and Variations in Systemic Immune and Inflammation Markers.JID innovations : skin science from molecules to population health · 2021
    Article
  14. NLRP3 Regulates IL-4 Expression in TOXFrontiers in immunology · 2021
    Article
  15. Article
  16. Article
  17. Article
  18. The Role of Interleukin-9 in Cancer.Pathology oncology research : POR · 2020
    Review
  19. IL-9 and IL-9-producing cells in tumor immunity.Cell communication and signaling : CCS · 2020
    Review
  20. 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

10 authors at 5 institutions in 4 countries.

Pablo A Vieyra-GarciaResearch Unit for Photodermatology, Department of Dermatology and Venereology, Medical University of Graz, Graz, Austria.
Tianling WeiDepartment of Dermatology, Bispebjerg Hospital, Copenhagen University Hospital, Copenhagen, Denmark.
David Gram NaymDepartment of Dermatology, Bispebjerg Hospital, Copenhagen University Hospital, Copenhagen, Denmark.
Simon FredholmDepartment of International Health, Immunology and Microbiology, University of Copenhagen, Copenhagen, Denmark.
Regina Fink-PuchesResearch Unit for Photodermatology, Department of Dermatology and Venereology, Medical University of Graz, Graz, Austria.
Lorenzo CerroniResearch Unit for Photodermatology, Department of Dermatology and Venereology, Medical University of Graz, Graz, Austria.
Niels OdumDepartment of International Health, Immunology and Microbiology, University of Copenhagen, Copenhagen, Denmark.
John T O'MalleyDepartment of Dermatology, Brigham and Women's Hospital, Harvard University, Boston, Massachusetts.
Robert GniadeckiDepartment of Dermatology, Bispebjerg Hospital, Copenhagen University Hospital, Copenhagen, Denmark. Division of Dermatology, Department of Medicine, University of Alberta, Edmonton, Canada.
Peter WolfResearch Unit for Photodermatology, Department of Dermatology and Venereology, Medical University of Graz, Graz, Austria. peter.wolf@medunigraz.at.
Medical University of Graz · ATBispebjerg Hospital · DKUniversity of Copenhagen · DKBrigham and Women's Hospital · USUniversity of Alberta · CA

Funding

The Next Generation Immunoanalysis CoreP30AR069625 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI CLARK, RACHAEL ANN · 2016 to 2025
$8.8M
DERMATOLOGY TRAINING GRANTT32AR007098 · NIAMS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI THOMAS S. KUPPER · 1986 to 2026
$8.1M
Austrian Science Fund FWF W 1241NIAMS NIH HHS P30 AR069625NIAMS NIH HHS T32 AR007098
6 · The paper itself

Abstract

purposeSustained inflammation is a key feature of mycosis fungoides (MF), the most common form of cutaneous T-cell lymphoma (CTCL). Resident IL9-producing T cells have been found in skin infections and certain inflammatory skin diseases, but their role in MF is currently unknown. EXPERIMENTAL

designWe analyzed lesional skin from patients with MF for the expression of IL9 and its regulators. To determine which cells were producing IL9, high-throughput sequencing was used to identify malignant clones and Vb-specific antibodies were employed to visualize malignant cells in histologic preparations. To explore the mechanism of IL9 secretion, we knocked down STAT3/5 and IRF4 by siRNA transfection in CTCL cell lines receiving psoralen+UVA (PUVA) ± anti-IL9 antibody. To further examine the role of IL9 in tumor development, the EL-4 T-cell lymphoma model was used in C57BL/6 mice.

resultsMalignant and reactive T cells produce IL9 in lesional skin. Expression of the Th9 transcription factor IRF4 in malignant cells was heterogeneous, whereas reactive T cells expressed it uniformly. PUVA or UVB phototherapy diminished the frequencies of IL9- and IL9r-positive cells, as well as STAT3/5a and IRF4 expression in lesional skin. IL9 production was regulated by STAT3/5 and silencing of STAT5 or blockade of IL9 with neutralizing antibodies potentiated cell death after PUVA treatment in vitro IL9-depleted mice exhibited a reduction of tumor growth, higher frequencies of regulatory T cells, and activated CD4 and CD8 T lymphocytes.

conclusionsOur results suggest that IL9 and its regulators are promising new targets for therapy development in mycosis fungoides. Clin Cancer Res; 22(13); 3328-39. ©2016 AACR.

Indexed as

AgedAged, 80 and overAnimalsCD8-Positive T-LymphocytesCell Line, TumorCell ProliferationCell SurvivalFemaleHigh-Throughput Nucleotide SequencingHumansInterferon Regulatory Factor-4Interferon Regulatory FactorsInterleukin-9Lymphocyte ActivationLymphocyte CountMaleIL9 protein, humanInterferon Regulatory Factor-4Interferon Regulatory FactorsInterleukin-9RNA, Small InterferingSTAT3 protein, humanSTAT3 Transcription FactorSTAT5A protein, humanSTAT5 Transcription FactorTumor Suppressor Proteins

Identifiers

PMID26851186
PMCPMC4967550
OpenAlexW2261762138

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.