Evidence map›Paper›PMID 27622024›Full record

ReviewOncoimmunology2016

Investigating potential exogenous tumor initiating and promoting factors for Cutaneous T-Cell Lymphomas (CTCL), a rare skin malignancy.

Ivan V Litvinov, Anna Shtreis, Kenneth Kobayashi, Steven Glassman, Matthew Tsang, Anders Woetmann, Denis Sasseville, Niels Ødum, Madeleine Duvic

Open access · goldAbstract readReview
In one paragraph

Review in Oncoimmunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
5.7field-weighted citation impact, top 4% 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, 1 synthesis or guideline pooled it, 50 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
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  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
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  11. Article
  12. Review
  13. The Role of Tumor Microenvironment in the Pathogenesis of Sézary Syndrome.International journal of molecular sciences · 2022
    Review
  14. Review
  15. Review
  16. Review
  17. Oncoimmunology · 2020
    Article
  18. Single-Cell Lymphocyte Heterogeneity in Advanced Cutaneous T-cell Lymphoma Skin Tumors.Clinical cancer research : an official journal of the American Association for Cancer Research · 2019
    Article
  19. 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

9 authors at 5 institutions in 3 countries.

Ivan V LitvinovDivision of Dermatology, Ottawa Hospital Research Institute, The University of Ottawa , Ottawa, ON, Canada.
Anna ShtreisDivision of Dermatology, Ottawa Hospital Research Institute, The University of Ottawa, Ottawa, ON, Canada; Division of Dermatology, McGill University, Montréal, QC, Canada.
Kenneth KobayashiDivision of Dermatology, Ottawa Hospital Research Institute, The University of Ottawa , Ottawa, ON, Canada.
Steven GlassmanDivision of Dermatology, Ottawa Hospital Research Institute, The University of Ottawa , Ottawa, ON, Canada.
Matthew TsangDivision of Dermatology, Ottawa Hospital Research Institute, The University of Ottawa , Ottawa, ON, Canada.
Anders WoetmannDepartment of Microbiology and Immunology, The University of Copenhagen , Copenhagen, Denmark.
Denis SassevilleDivision of Dermatology, McGill University , Montréal, QC, Canada.
Niels ØdumDepartment of Microbiology and Immunology, The University of Copenhagen , Copenhagen, Denmark.
Madeleine DuvicDepartment of Dermatology, The University of Texas MD Anderson Cancer Center , Houston, TX, USA.
University of Ottawa · CAOttawa Hospital · CAUniversity of Copenhagen · DKMcGill University · CAThe University of Texas MD Anderson Cancer Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Most skin malignancies are caused by external and often preventable environmental agents. Multiple reports demonstrated that cutaneous T-cell lymphomas (CTCL) can occur in married couples and cluster in families. Furthermore, recent studies document geographic clustering of this malignancy in Texas as well as in other areas of the United States. Multiple infectious, occupational, and medication causes have been proposed as triggers or promoters of this malignancy including hydrochlorothiazide diuretics, Staphylococcus aureus, dermatophytes, Mycobacterium leprae, Chlamydia pneumoniae, human T-Cell lymphotropic virus type 1 (HTLV1), Epstein-Barr virus (EBV), and herpes simplex virus (HSV). In this report, we review recent evidence evaluating the involvement of these agents in cancer initiation/progression. Most importantly, recent molecular experimental evidence documented for the first time that S. aureus can activate oncogenic STAT3 signaling in malignant T cells. Specifically, S. aureus Enterotoxin type A (SEA) was recently shown to trigger non-malignant infiltrating T cells to release IL-2 and other cytokines. These signals upon binging to their cognate receptors on malignant T cells are then able to activate STAT3 and STAT5 oncogenic signaling and promote cancer progression and IL-17 secretion. In light of these findings, it might be important for patients with exacerbation of their CTCL symptoms to maintain high index of suspicion and treat these individuals for S. aureus colonization and/or sepsis with topical and systemic antibiotics.

Indexed as

Cutaneous T-cell lymphoma (CTCL)HTLV-1 and geographic clusteringIL-17Mycosis fungoides (MF)S. aureusSézary syndrome (SS)STAT3viruses

Identifiers

PMID27622024
PMCPMC5006897
OpenAlexW2419661260

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.