Evidence map›Paper›PMID 34282767›Full record

ReviewCancers2021

Syndecan-4 in Tumor Cell Motility.

Aniko Keller-Pinter, Szuzina Gyulai-Nagy, Daniel Becsky, Laszlo Dux, Laszlo Rovo

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

30 citing papers in PubMed, 50 citations in OpenAlex.

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  11. Identification of dynamic network biomarkerMolecular therapy. Oncology · 2025
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  18. [Keloid nomogram prediction model based on weighted gene co-expression network analysis and machine learning].Sheng wu yi xue gong cheng xue za zhi = Journal of biomedical engineering = Shengwu yixue gongchengxue zazhi · 2023
    Article
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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

5 authors at 1 institution in 1 country.

Aniko Keller-PinterDepartment of Biochemistry, Faculty of Medicine, University of Szeged, H-6720 Szeged, Hungary.ORCID 0000-0002-4105-8458
Szuzina Gyulai-NagyDepartment of Biochemistry, Faculty of Medicine, University of Szeged, H-6720 Szeged, Hungary.
Daniel BecskyDepartment of Biochemistry, Faculty of Medicine, University of Szeged, H-6720 Szeged, Hungary.ORCID 0000-0002-7970-6000
Laszlo DuxDepartment of Biochemistry, Faculty of Medicine, University of Szeged, H-6720 Szeged, Hungary.
Laszlo RovoDepartment of Oto-Rhino-Laryngology and Head-Neck Surgery, University of Szeged, H-6725 Szeged, Hungary.
University of Szeged · HU

Funding

National Research, Development and Innovation Office of Hungary EFOP 3.6.3 VEKOP-16-2017 00009National Research, Development and Innovation Office of Hungary GINOP-2.3.2-15-2016-00040 (MYOTeam)National Research, Development and Innovation Office of Hungary NKFI FK 134684National Research, Development and Innovation Office of Hungary NKFI K 132446New National Excellence Program of the Ministry for Innovation and Technology Sciences UNKP-20-5-SZTE-162Szeged Scientists Academy under the sponsorship of the Hungarian Ministry of Innovation and Technology FEIF/433-4/2020-ITM_SZERZthe János Bolyai Research Scholarship of the Hungarian Academy of Sciences
6 · The paper itself

Abstract

Syndecan-4 (SDC4) is a ubiquitously expressed, transmembrane proteoglycan bearing heparan sulfate chains. SDC4 is involved in numerous inside-out and outside-in signaling processes, such as binding and sequestration of growth factors and extracellular matrix components, regulation of the activity of the small GTPase Rac1, protein kinase C-alpha, the level of intracellular calcium, or the phosphorylation of focal adhesion kinase. The ability of this proteoglycan to link the extracellular matrix and actin cytoskeleton enables SDC4 to contribute to biological functions like cell adhesion and migration, cell proliferation, cytokinesis, cellular polarity, or mechanotransduction. The multiple roles of SDC4 in tumor pathogenesis and progression has already been demonstrated; therefore, the expression and signaling of SDC4 was investigated in several tumor types. SDC4 influences tumor progression by regulating cell proliferation as well as cell migration by affecting cell-matrix adhesion and several signaling pathways. Here, we summarize the general role of SDC4 in cell migration and tumor cell motility.

Indexed as

actincalciumcancercell polaritycentrosomeEMTextracellular matrixmetastasismigrationproteoglycansyndecan-4

Identifiers

PMID34282767
PMCPMC8268284
OpenAlexW3176877288

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.