Evidence map›Paper›PMID 23801634›Full record

ArticleBlood2013

Elucidating the role of interleukin-17F in cutaneous T-cell lymphoma.

Thorbjørn Krejsgaard, Ivan V Litvinov, Yang Wang, Lixin Xia, Andreas Willerslev-Olsen, Sergei B Koralov, Katharina L Kopp, Charlotte M Bonefeld, Mariusz A Wasik, Carsten Geisler and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 1 pooled it
10.0field-weighted citation impact, top 2% 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

50 citing papers in PubMed, 1 synthesis or guideline pooled it, 96 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Article
  5. Role of Antigenic Stimulation in Cutaneous T-Cell Lymphomas.The Journal of investigative dermatology · 2024
    Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Differential Response of Mycosis Fungoides Cells to Vorinostat.International journal of molecular sciences · 2023
    Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Observational
  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

14 authors at 6 institutions in 4 countries.

Thorbjørn KrejsgaardDepartment of International Health, Immunology and Microbiology, University of Copenhagen, Blegdamsvej 3c, Copenhagen, Denmark.
Ivan V Litvinov
Yang Wang
Lixin Xia
Andreas Willerslev-Olsen
Sergei B Koralov
Katharina L Kopp
Charlotte M Bonefeld
Mariusz A Wasik
Carsten Geisler
Anders Woetmann
Youwen Zhou
Denis Sasseville
Niels Odum
University of Copenhagen · DKMcGill University Health Centre · CAUniversity of British Columbia · CANYU Langone Health · USPeking University · CNUniversity of Pennsylvania · US

Funding

UNIVERSITY OF PENNSYLVANIA CAN CTR SUPPORT GRANTP30CA016520 · NCI · UNIVERSITY OF PENNSYLVANIA · PI SHELLEY L BERGER · 1985 to 2026
$222.3M
Jak/STAT signaling in human T-cell lymphomasR01CA089194 · NCI · UNIVERSITY OF PENNSYLVANIA · PI WASIK, MARIUSZ A. · 2001 to 2010
$2.5M
NCI NIH HHS CA89194NCI NIH HHS P30 CA016520NCI NIH HHS R01 CA089194
6 · The paper itself

Abstract

Inappropriately regulated expression of interleukin (IL)-17A is associated with the development of inflammatory diseases and cancer. However, little is known about the role of other IL-17 family members in carcinogenesis. Here, we show that a set of malignant T-cell lines established from patients with cutaneous T-cell lymphoma (CTCL) spontaneously secrete IL-17F and that inhibitors of Janus kinases and Signal transducer and activator of transcription 3 are able to block that secretion. Other malignant T-cell lines produce IL-17A but not IL-17F. Upon activation, however, some of the malignant T-cell lines are able to coexpress IL-17A and IL-17F, leading to formation of IL-17A/F heterodimers. Clinically, we demonstrate that IL-17F messenger RNA expression is significantly increased in CTCL skin lesions compared with healthy donors and patients with chronic dermatitis. IL-17A expression is also increased and a significant number of patients express high levels of both IL-17A and IL-17F. Concomitantly, we observed that the expression of the IL-17 receptor is significantly increased in CTCL skin lesions compared with control subjects. Importantly, analysis of a historic cohort of 60 CTCL patients indicates that IL-17F expression is associated with progressive disease. These findings implicate IL-17F in the pathogenesis of CTCL and suggest that IL-17 cytokines and their receptors may serve as therapeutic targets.

Indexed as

Gene Expression RegulationGene Expression Regulation, NeoplasticBiopsyCell Line, TumorCytokinesDisease ProgressionFemaleHumansInterleukin-17Janus KinasesJurkat CellsLymphoma, T-Cell, CutaneousMaleMycosis FungoidesSkinSTAT3 Transcription FactorCytokinesInterleukin-17Janus KinasesSTAT3 protein, humanSTAT3 Transcription Factor

Identifiers

PMID23801634
PMCPMC3790948
OpenAlexW1978380394

What OpenQuestion holds

Textmetadata
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.