Evidence map›Paper›PMID 24402778›Full record

ArticleCancer medicine2014

Expression of FAP, ADAM12, WISP1, and SOX11 is heterogeneous in aggressive fibromatosis and spatially relates to the histologic features of tumor activity.

Benjamin S Misemer, Amy P N Skubitz, J Carlos Manivel, Stephen C Schmechel, Edward Y Cheng, Jonathan C Henriksen, Joseph S Koopmeiners, Christopher L Corless, Keith M Skubitz

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
0.3field-weighted citation impact, top 41% 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

21 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Differential [European journal of nuclear medicine and molecular imaging · 2026
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  8. Depletion of slow-cycling PDGFRαNature immunology · 2023
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  9. Review
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  11. Review
  12. CRISPR-SID: Identifying EZH2 as a druggable target for desmoid tumors via in vivo dependency mapping.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  13. Article
  14. Article
  15. Observational
  16. Article
  17. Article
  18. Article
  19. SOX11: friend or foe in tumor prevention and carcinogenesis?Therapeutic advances in medical oncology · 2019
    Review
  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 2 institutions in 1 country.

Benjamin S MisemerDepartment of Laboratory Medicine and Pathology, University of Minnesota Medical School, Minneapolis, Minnesota; Masonic Cancer Center, University of Minnesota Medical School, Minneapolis, Minnesota.
Amy P N Skubitz
J Carlos Manivel
Stephen C Schmechel
Edward Y Cheng
Jonathan C Henriksen
Joseph S Koopmeiners
Christopher L Corless
Keith M Skubitz
University of Minnesota Medical Center · USOregon Health & Science University · US

Funding

Women's CancerP30CA077598 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Douglas Yee · 1998 to 2026
$100.4M
Virological Measurements of Cryptic ReplicationP01AI074340 · NIAID · UNIVERSITY OF MINNESOTA · PI FLETCHER, COURTNEY V · 2008 to 2012
$12.1M
UAB / UMN SPORE in Pancreatic CancerP50CA101955 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BUCHSBAUM, DONALD J · 2010 to 2014
$11.1M
University of Minnesota Clinical and Translational Science Institute (UMN CTSI)KL2TR000113 · NCATS · UNIVERSITY OF MINNESOTA · PI BLAZAR, BRUCE R · 2012 to 2015
$5.4M
Antifibrotic Therapy to Improve Immune reconstitution in HIVR01AI093319 · NIAID · UNIVERSITY OF MINNESOTA · PI SCHACKER, TIMOTHY W · 2011 to 2014
$2.8M
University of Minnesota Clinical and Translational Science Institute (UMN CTSI)KL2RR033182 · NCRR · UNIVERSITY OF MINNESOTA · PI BLAZAR, BRUCE R · 2011 to 2011
$1.4M
NCATS NIH HHS KL2 TR000113NCI NIH HHS P30 CA077598NCI NIH HHS P30-CA77598NCI NIH HHS P50 CA101955NCI NIH HHS P50-CA101955NCRR NIH HHS KL2 RR033182NCRR NIH HHS KL2-RR033182NIAID NIH HHS P01 AI074340NIAID NIH HHS R01 AI093319
6 · The paper itself

Abstract

Aggressive fibromatosis (AF) represents a group of tumors with a variable and unpredictable clinical course, characterized by a monoclonal proliferation of myofibroblastic cells. The optimal treatment for AF remains unclear. Identification and validation of genes whose expression patterns are associated with AF may elucidate biological mechanisms in AF, and aid treatment selection. This study was designed to examine the protein expression by immunohistochemistry (IHC) of four genes, ADAM12, FAP, SOX11, and WISP1, that were found in an earlier study to be uniquely overexpressed in AF compared with normal tissues. Digital image analysis was performed to evaluate inter- and intratumor heterogeneity, and correlate protein expression with histologic features, including a histopathologic assessment of tumor activity, defined by nuclear chromatin density ratio (CDR). AF tumors exhibited marked inter- and intratumor histologic heterogeneity. Pathologic assessment of tumor activity and digital assessment of average nuclear size and CDR were all significantly correlated. IHC revealed protein expression of all four genes. IHC staining for ADAM12, FAP, and WISP1 correlated with CDR and was higher, whereas SOX11 staining was lower in tumors with earlier recurrence following excision. All four proteins were expressed, and the regional variation in tumor activity within and among AF cases was demonstrated. A spatial correlation between protein expression and nuclear morphology was observed. IHC also correlated with the probability of recurrence following excision. These proteins may be involved in AF pathogenesis and the corresponding pathways could serve as potential targets of therapy.

Indexed as

ADAM12 ProteinADAM ProteinsCCN Intercellular Signaling ProteinsChromatinDesmoid TumorsEndopeptidasesFibroblast Activation Protein AlphaGelatinasesGene Expression Regulation, NeoplasticGenetic HeterogeneityHumansMembrane ProteinsProto-Oncogene ProteinsSerine EndopeptidasesSOXC Transcription FactorsADAM12 ProteinADAM12 protein, humanADAM ProteinsCCN4 protein, humanCCN Intercellular Signaling ProteinsChromatinEndopeptidasesFibroblast Activation Protein AlphaGelatinasesMembrane ProteinsProto-Oncogene ProteinsSerine EndopeptidasesSOX11 protein, humanSOXC Transcription FactorsADAM12desmoidsFAPfibromatosisSOX11WISP1

Identifiers

PMID24402778
PMCPMC3930392
OpenAlexW1971253093

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.