Evidence map›Paper›PMID 25320080›Full record

ArticleThe Journal of biological chemistry2014

A role for versican in the development of leiomyosarcoma.

Paul A Keire, Steven L Bressler, Joan M Lemire, Badreddin Edris, Brian P Rubin, Maziar Rahmani, Bruce M McManus, Matt van de Rijn, Thomas N Wight

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.4field-weighted citation impact, top 12% 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, 35 citations in OpenAlex.

  1. VCAN Is Essential for ERK5-Driven Tumorigenesis in Soft Tissue Sarcoma.International journal of biological sciences · 2026
    Article
  2. Review
  3. Article
  4. V3: an enigmatic isoform of the proteoglycan versican.American journal of physiology. Cell physiology · 2023
    Review
  5. Article
  6. Multi-modal Profiling of the Extracellular Matrix of Human Fallopian Tubes and Serous Tubal Intraepithelial Carcinomas.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2022
    Article
  7. Versican and Versican-matrikines in Cancer Progression, Inflammation, and Immunity.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2020
    Review
  8. Review
  9. Sarcoma Tumor Microenvironment.Advances in experimental medicine and biology · 2020
    Article
  10. Article
  11. Charting the unexplored extracellular matrix in cancer.International journal of experimental pathology · 2018
    Review
  12. Review
  13. Article
  14. Provisional matrix: A role for versican and hyaluronan.Matrix biology : journal of the International Society for Matrix Biology · 2017
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Proteoglycan form and function: A comprehensive nomenclature of proteoglycans.Matrix biology : journal of the International Society for Matrix Biology · 2015
    Review
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 2 countries.

Paul A KeireFrom the Matrix Biology Program, Benaroya Research Institute at Virginia Mason, Seattle, Washington 98101, Department of Pathology, University of Washington, Seattle, Washington 98195.
Steven L BresslerFrom the Matrix Biology Program, Benaroya Research Institute at Virginia Mason, Seattle, Washington 98101.
Joan M LemireDepartment of Pathology, University of Washington, Seattle, Washington 98195.
Badreddin EdrisDepartment of Pathology, Stanford University School of Medicine, Stanford, California 94305, and.
Brian P RubinDepartment of Pathology, University of Washington, Seattle, Washington 98195.
Maziar RahmaniJames Hogg iCAPTURE Centre for Cardiovascular and Pulmonary Research, St. Paul's Hospital, Room 166, 1081 Burrard Street, Vancouver, British Columbia V6Z 1Y6, Canada, and Department of Pathology and Laboratory Medicine, University of British Columbia, Room G227, 2211 Wesbrook Mall, Vancouver, British Columbia V6T 2A1, Canada.
Bruce M McManusJames Hogg iCAPTURE Centre for Cardiovascular and Pulmonary Research, St. Paul's Hospital, Room 166, 1081 Burrard Street, Vancouver, British Columbia V6Z 1Y6, Canada, and Department of Pathology and Laboratory Medicine, University of British Columbia, Room G227, 2211 Wesbrook Mall, Vancouver, British Columbia V6T 2A1, Canada.
Matt van de RijnDepartment of Pathology, Stanford University School of Medicine, Stanford, California 94305, and.
Thomas N WightFrom the Matrix Biology Program, Benaroya Research Institute at Virginia Mason, Seattle, Washington 98101, Department of Pathology, University of Washington, Seattle, Washington 98195, twight@benaroyaresearch.org.
University of Washington · USBenaroya Research InstituteSt. Paul's Hospital · CAStanford Medicine · USStanford University · US

Funding

INSTITUTIONAL TRAINING GRANT IN GENOME SCIENCET32HG000044 · NHGRI · STANFORD UNIVERSITY · PI MICHAEL P. SNYDER · 1995 to 2026
$32.2M
Thymic Stromal Lymphopoietin (TSLP) and Lung Inflammation and ImmP01HL098067 · NHLBI · BENAROYA RESEARCH INST AT VIRGINIA MASON · PI FREVERT, CHARLES WAYNE · 2010 to 2014
$13.5M
Molecular Characterization of Leiomyosarcoma and GISTR01CA112270 · NCI · STANFORD UNIVERSITY · PI VAN DE RIJN, JAN MATT · 2005 to 2014
$3.0M
NCI NIH HHS CA112270NCI NIH HHS R01 CA112270NHGRI NIH HHS 5 T32 HG00044NHGRI NIH HHS T32 HG000044NHLBI NIH HHS HL098067NHLBI NIH HHS P01 HL098067
6 · The paper itself

Abstract

Leiomyosarcoma (LMS) is a mesenchymal cancer that occurs throughout the body. Although LMS is easily recognized histopathologically, the cause of the disease remains unknown. Versican, an extracellular matrix proteoglycan, increases in LMS. Microarray analyses of 80 LMSs and 24 leiomyomas showed a significant elevated expression of versican in human LMS versus benign leiomyomas. To explore the importance of versican in this smooth muscle cell tumor, we used versican-directed siRNA to knock down versican expression in a LMS human cell line, SK-LMS-1. Decreased versican expression was accompanied by slower rates of LMS cell proliferation and migration, increased adhesion, and decreased accumulation of the extracellular matrix macromolecule hyaluronan. Addition of purified versican to cells expressing versican siRNA restored cell proliferation to the level of LMS controls, increased the pericellular coat and the retention of hyaluronan, and decreased cell adhesion in a dose-dependent manner. The presence of versican was not only synergistic with hyaluronan in increasing cell proliferation, but the depletion of versican decreased hyaluronan synthase expression and decreased the retention of hyaluronan. When LMS cells stably expressing versican siRNA were injected into nude mice, the resulting tumors displayed significantly less versican and hyaluronan staining, had lower volumes, and had reduced levels of mitosis as compared with controls. Collectively, these results suggest a role for using versican as a point of control in the management and treatment of LMS.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsCell AdhesionCell Line, TumorCell MovementCell ProliferationGene Expression ProfilingGlucuronosyltransferaseHumansHyaluronan SynthasesHyaluronic AcidLeiomyosarcomaMiceMice, NudeMuscle NeoplasmsMuscle, SmoothGlucuronosyltransferaseHyaluronan SynthasesHyaluronic AcidRNA, Small InterferingVersicansCell MigrationCell ProliferationExtracellular MatrixHyaluronanLeiomyosarcomaSmall Interfering RNA (siRNA)Tumor GrowthVersican

Identifiers

PMID25320080
PMCPMC4256343
OpenAlexW2029404470

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.