Evidence map›Paper›PMID 24497534›Full record

ArticleBlood2014

GATA-3 expression identifies a high-risk subset of PTCL, NOS with distinct molecular and clinical features.

Tianjiao Wang, Andrew L Feldman, David A Wada, Ye Lu, Avery Polk, Robert Briski, Kay Ristow, Thomas M Habermann, Dafydd Thomas, Steven C Ziesmer and 9 more

Open access · greenAbstract read
In one paragraph

Article in Blood, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 115 papers.

0numbers the graph read from it
0cells of the map it votes in
115citing papers in PubMed
7.2field-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

115 citing papers in PubMed, 180 citations in OpenAlex.

  1. Trial
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  4. Article
  5. Novel agents and therapeutic advances in T cell lymphoma.International journal of hematology · 2026
    Review
  6. Review
  7. Article
  8. Article
  9. The Significance of the Microenvironment in T/Nk-Cell Neoplasms.International journal of molecular sciences · 2025
    Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Characterizing Nodal Gamma-Delta T-Cell Lymphoma: Clinicopathological and Molecular Insights.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2025
    Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. Article

55 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 4 institutions in 1 country.

Tianjiao WangDivision of Hematology and Oncology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI;
Andrew L Feldman
David A Wada
Ye Lu
Avery Polk
Robert Briski
Kay Ristow
Thomas M Habermann
Dafydd Thomas
Steven C Ziesmer
Linda E Wellik
Thomas M Lanigan
Thomas E Witzig
Mark R Pittelkow
Nathanael G Bailey
Alexandra C Hristov
Megan S Lim
Stephen M Ansell
Ryan A Wilcox
Mayo Clinic in Arizona · USUniversity of Michigan–Ann Arbor · USMayo Clinic · USUniversity of Utah · US

Funding

The role of GATA-3 in T-cell lymphomasK08CA172215 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WILCOX, RYAN A · 2013 to 2017
$893k
NCI NIH HHS K08 CA172215NCI NIH HHS K08CA172215
6 · The paper itself

Abstract

The cell of origin and the tumor microenvironment's role remain elusive for the most common peripheral T-cell lymphomas (PTCLs). As macrophages promote the growth and survival of malignant T cells and are abundant constituents of the tumor microenvironment, their functional polarization was examined in T-cell lymphoproliferative disorders. Cytokines that are abundant within the tumor microenvironment, particularly interleukin (IL)-10, were observed to promote alternative macrophage polarization. Macrophage polarization was signal transducer and activator of transcription 3 dependent and was impaired by the Janus kinase inhibitor ruxolitinib. In conventional T cells, the production of T helper (Th)2-associated cytokines and IL-10, both of which promote alternative macrophage polarization, is regulated by the T-cell transcription factor GATA-binding protein 3 (GATA-3). Therefore, its role in the T-cell lymphomas was examined. GATA-3 expression was observed in 45% of PTCLs, not otherwise specified (PTCL, NOS) and was associated with distinct molecular features, including the production of Th2-associated cytokines. In addition, GATA-3 expression identified a subset of PTCL, NOS with distinct clinical features, including inferior progression-free and overall survival. Collectively, these data suggest that further understanding the cell of origin and lymphocyte ontogeny among the T-cell lymphomas may improve our understanding of the tumor microenvironment's pathogenic role in these aggressive lymphomas.

Indexed as

Blotting, WesternCell Line, TumorCytokinesGATA3 Transcription FactorGene Expression Regulation, NeoplasticHumansImmunohistochemistryInterleukin-10Kaplan-Meier EstimateLymphoma, T-Cell, PeripheralMacrophagesNitrilesPyrazolesPyrimidinesReverse Transcriptase Polymerase Chain ReactionRisk FactorsCytokinesGATA3 protein, humanGATA3 Transcription FactorInterleukin-10NitrilesPyrazolesPyrimidinesruxolitinib

Identifiers

PMID24497534
PMCPMC4014843
OpenAlexW2067999861

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.