Evidence map›Paper›PMID 19506550›Full record

ArticleLaboratory investigation; a journal of technical methods and pathology2009

S100A4 mediates endometrial cancer invasion and is a target of TGF-beta1 signaling.

Ran Xie, Matthew P Schlumbrecht, Gregory L Shipley, Susu Xie, Roland L Bassett, Russell R Broaddus

Open access · greenAbstract read
In one paragraph

Article in Laboratory investigation; a journal of technical methods and pathology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

26 citing papers in PubMed, 54 citations in OpenAlex.

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  13. Endometrial cancer among a cohort of urban Haitian immigrants.World journal of clinical oncology · 2019
    Article
  14. Article
  15. S100A4 amplifies TGF-β-induced epithelial-mesenchymal transition in a pleural mesothelial cell line.Journal of investigative medicine : the official publication of the American Federation for Clinical Research · 2018
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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

6 authors at 2 institutions in 1 country.

Ran XieDepartment of Pathology, University of Texas M.D. Anderson Cancer Center, Houston, TX, USA.
Matthew P Schlumbrecht
Gregory L Shipley
Susu Xie
Roland L Bassett
Russell R Broaddus
The University of Texas MD Anderson Cancer Center · USThe University of Texas Health Science Center at Houston · US

Funding

Targeting the PI3K Signaling Pathway in Endometrial CarcinomaP50CA098258 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI BODURKA, DIANE · 2003 to 2020
$32.0M
NCI NIH HHS 1P50CA098258-01NCI NIH HHS P50 CA098258
6 · The paper itself

Abstract

The molecular mechanisms of endometrial cancer invasion are poorly understood. S100A4, also known as FSP1 (fibroblast-specific protein 1), has long been known to be a molecular marker of fibrosis in a variety of different fibrotic diseases of the lungs, liver, kidney, and heart. We demonstrate here that increased expression of S100A4 is associated with advanced stage endometrial cancer and decreased recurrence free survival. To verify the essential role of S100A4 in invasiveness of endometrial cancer, S100A4 expression was downregulated by RNAi in HEC-1A cells, which resulted in undetectable S100A4 protein and significantly decreased migration and invasion. Owing to the established connection between TGF-beta1 and S100A4 induction in experimental models of kidney and liver fibrosis, we next examined whether TGF-beta1 could also regulate S100A4 in endometrial cancer cells. TGF-beta1 stimulated endometrial cancer cell migration and invasion with a concomitant increase in S100A4 protein. Induction of S100A4 was associated with the activation of Smads. TGF-beta1-mediated endometrial cancer cell motility was inhibited by S100A4 siRNA. In aggregate, these results suggest that S100A4 is a critical mediator of invasion in endometrial cancer and is upregulated by the TGF-beta1 signaling pathway. These results also suggest that endometrial cancer cell invasion and fibrosis share common molecular mechanisms.

Indexed as

AdenocarcinomabetaIG-H3 ProteinCell Line, TumorCell MovementCell ProliferationEndometrial NeoplasmsEndometriumExtracellular Matrix ProteinsFemaleGene ExpressionGene Knockdown TechniquesGene SilencingHumansNeoplasm InvasivenessRNA, Small InterferingS100 Calcium-Binding Protein A4betaIG-H3 ProteinExtracellular Matrix ProteinsRNA, Small InterferingS100A4 protein, humanS100 Calcium-Binding Protein A4S100 ProteinsTransforming Growth Factor beta

Identifiers

PMID19506550
PMCPMC2718065
OpenAlexW1972141788

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.