Evidence map›Paper›PMID 22232518›Full record

ArticleMolecular cancer research : MCR2012

WNT7A regulates tumor growth and progression in ovarian cancer through the WNT/β-catenin pathway.

Shin Yoshioka, Mandy L King, Sophia Ran, Hiroshi Okuda, James A MacLean, Mary E McAsey, Norihiro Sugino, Laurent Brard, Kounosuke Watabe, Kanako Hayashi

Open access · greenAbstract read
In one paragraph

Article in Molecular cancer research : MCR, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 112 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
112citing papers in PubMed, 1 pooled it
5.9field-weighted citation impact, top 3% 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

112 citing papers in PubMed, 1 synthesis or guideline pooled it, 168 citations in OpenAlex.

  1. Pooled it
  2. Review
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  8. Review
  9. Article
  10. Emerging roles and biomarker potential of WNT6 in human cancers.Cell communication and signaling : CCS · 2024
    Review
  11. Wnt signaling and tumors (Review).Molecular and clinical oncology · 2024
    Review
  12. Article
  13. Article
  14. Article
  15. Article
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52 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

10 authors at 2 institutions in 2 countries.

Shin YoshiokaDepartment of Physiology, Southern Illinois University School of Medicine, 1135 Lincoln Drive, Carbondale, IL 62901, USA.
Mandy L King
Sophia Ran
Hiroshi Okuda
James A MacLean
Mary E McAsey
Norihiro Sugino
Laurent Brard
Kounosuke Watabe
Kanako Hayashi
Southern Illinois University School of Medicine · USYamaguchi University · JP

Funding

Functional Role of Wnt11 in Uterine Development and Adult FunctionR03HD058222 · NICHD · SOUTHERN ILLINOIS UNIVERSITY CARBONDALE · PI HAYASHI, KANAKO · 2009 to 2010
$173k
NICHD NIH HHS HD058222NICHD NIH HHS R03 HD058222
6 · The paper itself

Abstract

Abnormal activation the WNT/β-catenin signaling pathway has been associated with ovarian carcinomas, but a specific WNT ligand and pertinent downstream mechanisms are not fully understood. In this study, we found abundant WNT7A in the epithelium of serous ovarian carcinomas, but not detected in borderline and benign tumors, normal ovary, or endometrioid carcinomas. To characterize the role of WNT7A in ovarian tumor growth and progression, nude mice were injected either intraperitoneally or subcutaneously with WNT7A knocked down SKOV3.ip1 and overexpressed SKOV3 cells. In the intraperitoneal group, mice receiving SKOV3.ip1 cells with reduced WNT7A expression developed significantly fewer tumor lesions. Gross and histologic examination revealed greatly reduced invasion of WNT7A knockdown cells into intestinal mesentery and serosa compared with the control cells. Tumor growth was regulated by loss or overexpression of WNT7A in mice receiving subcutaneous injection as well. In vitro analysis of cell function revealed that cell proliferation, adhesion, and invasion were regulated by WNT7A. The activity of the T-cell factor/lymphoid enhancer factor (TCF/LEF) reporter was stimulated by overexpression of WNT7A in ovarian cancer cells. Cotransfection with WNT7A and FZD5 receptor further increased activity, and this effect was inhibited by cotransfection with SFRP2 or dominant negative TCF4. Overexpression of WNT7A stimulated matrix metalloproteinase 7 (MMP7) promoter, and mutation of TCF-binding sites in MMP7 promoter confirmed that activation of MMP7 promoter by WNT7A was mediated by β-catenin/TCF signaling. Collectively, these results suggest that reexpression of WNT7A during malignant transformation of ovarian epithelial cells plays a critical role in ovarian cancer progression mediated by WNT/β-catenin signaling pathway.

Indexed as

Disease ProgressionWnt Signaling PathwayAnimalsBase Sequencebeta CateninCarcinoma, Ovarian EpithelialCell AdhesionCell Line, TumorCell ProliferationFemaleFrizzled ReceptorsGene Expression Regulation, NeoplasticGene Knockdown TechniquesHumansMatrix Metalloproteinase 7Micebeta CateninFrizzled ReceptorsFZD5 protein, humanMatrix Metalloproteinase 7MMP7 protein, humanTCF Transcription FactorsWNT7A protein, humanWnt Proteins

Identifiers

PMID22232518
PMCPMC3307825
OpenAlexW2127754060

What OpenQuestion holds

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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.