Evidence map›Paper›PMID 29128259›Full record

ArticleThe Journal of investigative dermatology2018

Role of Dysregulated Cytokine Signaling and Bacterial Triggers in the Pathogenesis of Cutaneous T-Cell Lymphoma.

Melania H Fanok, Amy Sun, Laura K Fogli, Vijay Narendran, Miriam Eckstein, Kasthuri Kannan, Igor Dolgalev, Charalampos Lazaris, Adriana Heguy, Mary E Laird and 10 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of investigative dermatology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed, 2 pooled it
7.8field-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

54 citing papers in PubMed, 2 syntheses or guidelines pooled it, 96 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  8. Review
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  10. Article
  11. RuBi-Ruxolitinib: A Photoreleasable Antitumor JAK Inhibitor.Journal of the American Chemical Society · 2024
    Article
  12. Role of Antigenic Stimulation in Cutaneous T-Cell Lymphomas.The Journal of investigative dermatology · 2024
    Review
  13. Article
  14. "Next top" mouse models advancing CTCL research.Frontiers in cell and developmental biology · 2024
    Review
  15. Review
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  17. Article
  18. Article
  19. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 4 institutions in 2 countries.

Melania H FanokDepartment of Pathology, New York University School of Medicine, New York, New York, USA.
Amy SunDepartment of Pathology, New York University School of Medicine, New York, New York, USA.
Laura K FogliDepartment of Pathology, New York University School of Medicine, New York, New York, USA.
Vijay NarendranDepartment of Medicine, Division of Hematology-Oncology, New York University School of Medicine, New York, New York, USA.
Miriam EcksteinDepartment of Basic Science and Craniofacial Biology, NYU College of Dentistry, New York, New York, USA.
Kasthuri KannanDepartment of Pathology, New York University School of Medicine, New York, New York, USA; Office of Collaborative Science, New York University School of Medicine, New York, New York, USA.
Igor DolgalevDepartment of Pathology, New York University School of Medicine, New York, New York, USA; Office of Collaborative Science, New York University School of Medicine, New York, New York, USA.
Charalampos LazarisDepartment of Pathology, New York University School of Medicine, New York, New York, USA; Laura and Isaac Perlmutter Cancer Institute, New York University School of Medicine, New York, New York, USA.
Adriana HeguyDepartment of Pathology, New York University School of Medicine, New York, New York, USA; Office of Collaborative Science, New York University School of Medicine, New York, New York, USA.
Mary E LairdThe Ronald O. Perelman Department of Dermatology, New York University School of Medicine, New York, New York, USA.
Mark S SundrudDepartment of Immunology and Microbiology, The Scripps Research Institute, Jupiter, Florida, USA.
Cynthia LiuDepartment of Pathology, New York University School of Medicine, New York, New York, USA.
Jeff KutokDepartment of Pathology, Brigham and Women's Hospital; Boston, Massachusetts, USA.
Rodrigo S LacruzDepartment of Basic Science and Craniofacial Biology, NYU College of Dentistry, New York, New York, USA.
Jo-Ann LatkowskiThe Ronald O. Perelman Department of Dermatology, New York University School of Medicine, New York, New York, USA.
Iannis AifantisDepartment of Pathology, New York University School of Medicine, New York, New York, USA; Laura and Isaac Perlmutter Cancer Institute, New York University School of Medicine, New York, New York, USA.
Niels ØdumDepartment of International Health, Immunology and Microbiology, University of Copenhagen, Copenhagen, Denmark.
Kenneth B HymesDepartment of Medicine, Division of Hematology-Oncology, New York University School of Medicine, New York, New York, USA; Department of Pathology, Brigham and Women's Hospital; Boston, Massachusetts, USA.
Swati GoelDepartment of Medicine, Division of Hematology-Oncology, New York University School of Medicine, New York, New York, USA.
Sergei B KoralovDepartment of Pathology, New York University School of Medicine, New York, New York, USA; Laura and Isaac Perlmutter Cancer Institute, New York University School of Medicine, New York, New York, USA. Electronic address: sergei.koralov@med.nyu.edu.
New York University · USBrigham and Women's Hospital · USScripps Research Institute · USUniversity of Copenhagen · DK

Funding

Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ADRIANA HEGUY · 1985 to 2026
$83.1M
MEDICAL SCIENTIST TRAININGT32GM007308 · NIGMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI PHILIPS, MARK REID · 1985 to 2019
$23.2M
TRAINING PROGRAM IN MOLECULAR ONCOLOGY &IMMUNOLOGYT32CA009161 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI CARROLL, WILLIAM L., LEVY, DAVID E · 1985 to 2020
$13.3M
Training Program in Immunology and Inflammation.T32AI100853 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Susan Ruth Schwab · 2012 to 2026
$4.5M
Microbial triggers and molecular mechanisms of Th17 mediated airway inflammation-Resubmission-1R01HL125816 · NHLBI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI KORALOV, SERGEI BORISOVICH · 2015 to 2019
$3.3M
Calcium Control of Enamel DevelopmentR01DE025639 · NIDCR · NEW YORK UNIVERSITY · PI LACRUZ, RODRIGO S. · 2016 to 2020
$2.0M
Generation of a mouse expressing a photoactivatable Cre recombinaseR21AI124129 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI KORALOV, SERGEI BORISOVICH, SCHWAB, SUSAN RUTH · 2016 to 2017
$466k
Ventana Medical Systems Discovery XTS10OD010584 · OD · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI CHIRIBOGA, LUIS A · 2013 to 2013
$127k
Sandy Recovery Ventana Medical Systems Discovery XTS10OD018338 · OD · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI CHIRIBOGA, LUIS A · 2014 to 2014
$123k
STAT3: At the Crossroads of Inflammation and CancerF31CA171596 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI FOGLI, LAURA KATHERINE · 2013 to 2015
$58k
Uncovering Antigenic and Microbial Contributors to the Pathogenesis of Cutaneous T Cell LymphomaF31AR070094 · NIAMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI FANOK, MELANIA H · 2017 to 2017
$37k
NCI NIH HHS F31 CA171596NCI NIH HHS P30 CA016087NCI NIH HHS T32 CA009161NHLBI NIH HHS R01 HL125816NIAID NIH HHS R21 AI124129NIAID NIH HHS T32 AI100853NIAMS NIH HHS F31 AR070094NIDCR NIH HHS R01 DE025639NIGMS NIH HHS T32 GM007308NIH HHS S10 OD010584NIH HHS S10 OD018338
6 · The paper itself

Abstract

Cutaneous T-cell lymphoma is a heterogeneous group of lymphomas characterized by the accumulation of malignant T cells in the skin. The molecular and cellular etiology of this malignancy remains enigmatic, and what role antigenic stimulation plays in the initiation and/or progression of the disease remains to be elucidated. Deep sequencing of the tumor genome showed a highly heterogeneous landscape of genetic perturbations, and transcriptome analysis of transformed T cells further highlighted the heterogeneity of this disease. Nonetheless, using data harvested from high-throughput transcriptional profiling allowed us to develop a reliable signature of this malignancy. Focusing on a key cytokine signaling pathway previously implicated in cutaneous T-cell lymphoma pathogenesis, JAK/STAT signaling, we used conditional gene targeting to develop a fully penetrant small animal model of this disease that recapitulates many key features of mycosis fungoides, a common variant of cutaneous T-cell lymphoma. Using this mouse model, we show that T-cell receptor engagement is critical for malignant transformation of the T lymphocytes and that progression of the disease is dependent on microbiota.

Indexed as

AnimalsCytokinesDisease Models, AnimalDNA Copy Number VariationsGene Expression ProfilingHigh-Throughput Nucleotide SequencingHumansLymphoma, T-Cell, CutaneousMiceMicrobiotaReceptors, Antigen, T-CellSezary SyndromeSignal TransductionSkin NeoplasmsSTAT3 Transcription FactorCytokinesReceptors, Antigen, T-CellSTAT3 Transcription Factor

Identifiers

PMID29128259
PMCPMC5912980
OpenAlexW2767327745

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.