Evidence map›Paper›PMID 25873501›Full record

ArticleAmerican journal of clinical pathology2015

Extensive survey of STAT6 expression in a large series of mesenchymal tumors.

Elizabeth G Demicco, Paul W Harms, Rajiv M Patel, Steven C Smith, Davis Ingram, Keila Torres, Shannon L Carskadon, Sandra Camelo-Piragua, Jonathan B McHugh, Javed Siddiqui and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in American journal of clinical pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 86 papers.

0numbers the graph read from it
0cells of the map it votes in
86citing papers in PubMed
16.9field-weighted citation impact, top 1% 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

86 citing papers in PubMed, 203 citations in OpenAlex.

  1. Article
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  4. Article
  5. Solitary fibrous tumor: an updated review.Journal of pathology and translational medicine · 2026
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26 more citing papers are in PubMed but not listed here.

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 3 institutions in 1 country.

Elizabeth G DemiccoFrom Pathology, Icahn School of Medicine at Mount Sinai, New York, NY; Elizabeth.Demicco@mountsinai.org.
Paul W HarmsPathology, University of Michigan Medical Center, Ann Arbor; and.
Rajiv M PatelPathology, University of Michigan Medical Center, Ann Arbor; and.
Steven C SmithPathology, University of Michigan Medical Center, Ann Arbor; and.
Davis IngramPathology.
Keila TorresSarcoma Research Center, and Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston.
Shannon L CarskadonPathology, University of Michigan Medical Center, Ann Arbor; and.
Sandra Camelo-PiraguaPathology, University of Michigan Medical Center, Ann Arbor; and.
Jonathan B McHughPathology, University of Michigan Medical Center, Ann Arbor; and.
Javed SiddiquiPathology, University of Michigan Medical Center, Ann Arbor; and.
Nallasivam PalanisamyPathology, University of Michigan Medical Center, Ann Arbor; and.
David R LucasPathology, University of Michigan Medical Center, Ann Arbor; and.
Alexander J LazarPathology, Sarcoma Research Center, and.
Wei-Lien WangPathology.
University of Michigan–Ann Arbor · USThe University of Texas MD Anderson Cancer Center · USIcahn School of Medicine at Mount Sinai · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Axl receptor signaling in MPNST; potential node for therapyK08CA160443 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI TORRES, KEILA ENITT · 2012 to 2016
$853k
NCI NIH HHS K08 CA160443NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

objectivesExpression of strong nuclear STAT6 is thought to be a specific marker for solitary fibrous tumors (SFTs). Little is known about subtle expression patterns in other mesenchymal lesions.

methodsWe performed immunohistochemical studies against the C-terminus of STAT6 in tissue microarrays and whole sections, comprising 2366 mesenchymal lesions.

resultsStrong nuclear STAT6 was expressed in 285 of 2,021 tumors, including 206 of 240 SFTs, 49 of 408 well-differentiated/dedifferentiated liposarcomas, eight of 65 unclassified sarcomas, and 14 of 184 desmoid tumors, among others. Expression in SFTs was predominately limited to the nucleus. Other positive tumors typically expressed both nuclear and cytoplasmic STAT6. Complete absence of STAT6 was most common in pleomorphic liposarcoma and alveolar soft part sarcoma (60% and 72% cases negative, respectively).

conclusionsStrong nuclear STAT6 is largely specific for SFTs. Physiologic low-level cytoplasmic/nuclear expression is common in mesenchymal neoplasia and is of uncertain significance.

Indexed as

Biomarkers, TumorCell NucleusChildChild, PreschoolHumansImmunohistochemistryLiposarcomaSarcomaSensitivity and SpecificitySoft Tissue NeoplasmsSolitary Fibrous TumorsSTAT6 Transcription FactorTissue Array AnalysisBiomarkers, TumorSTAT6 protein, humanSTAT6 Transcription FactorImmunohistochemistrySarcomaSolitary fibrous tumorSTAT6

Identifiers

PMID25873501
PMCPMC4505928
OpenAlexW1991963614

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.