Evidence map›Paper›PMID 23128109›Full record

ReviewJournal of dental research2013

Biomarkers of epithelial-mesenchymal transition in squamous cell carcinoma.

C S Scanlon, E A Van Tubergen, R C Inglehart, N J D'Silva

Abstract readReview
In one paragraph

Review in Journal of dental research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 179 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
179citing papers in PubMed, 4 pooled it
9.9field-weighted citation impact, top 1% 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

179 citing papers in PubMed, 4 syntheses or guidelines pooled it, 326 citations in OpenAlex.

  1. Pooled it
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  12. Nutrition research and practice · 2025
    Article
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  15. Targeting MAPK Signaling: Loureirins A and B fromLife (Basel, Switzerland) · 2025
    Article
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  17. Review
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  19. Article
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119 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

4 authors at 1 institution in 1 country.

C S ScanlonPeriodontics and Oral Medicine, School of Dentistry, University of Michigan, Ann Arbor, MI, USA.
E A Van Tubergen
R C Inglehart
N J D'Silva
University of Michigan–Ann Arbor · US

Funding

Role of Rap1 in cadherin and integrin mediated cross-talk in oral keratinocytesR01DE018512 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI D'SILVA, NISHA J · 2007 to 2011
$1.7M
Biomarkers in Head and Neck Cancer ProgressionK02DE019513 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI D'SILVA, NISHA J · 2009 to 2013
$472k
Characterization of the Immunomic Profile of Head and Neck CancerR21DE017977 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI D'SILVA, NISHA J · 2008 to 2009
$418k
Head and neck cancer:Role of NFATc 2 in GALR2-mediatedtumor progressionF30DE021293 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SCANLON, CHRISTINA SPRINGSTEAD · 2010 to 2012
$128k
NIDCR NIH HHS DE017977NIDCR NIH HHS DE018512NIDCR NIH HHS DE019513NIDCR NIH HHS F30 DE021293NIDCR NIH HHS F32 DE213052NIDCR NIH HHS K02 DE019513NIDCR NIH HHS R01 DE018512NIDCR NIH HHS R21 DE017977
6 · The paper itself

Abstract

An understanding of the process by which tumor cells destroy the basement membrane of the surface epithelium, invade, and metastasize is essential to the development of novel treatment of head and neck squamous cell carcinoma (HNSCC). In recent years, there has been increased interest in the role of epithelial-mesenchymal transition (EMT) in invasion. EMT is a process that describes the development of motile, mesenchymal-like cells from non-motile parent epithelial cells. There are 3 known types of EMT that mediate development, wound healing, and carcinogenesis. This review summarizes studies of known EMT biomarkers in the context of HNSCC progression. The biomarkers discussed come from a wide range of proteins, including cell-surface proteins (E-cadherin, N-cadherin, and Integrins), cytoskeletal proteins (α-Smooth Muscle Actin, Vimentin, and β-catenin), extracellular matrix proteins (Collagens, Fibronectin, and Laminin), and transcription factors (SNAIL1, SNAIL2, TWIST, and LEF-1). Overall, the findings of these studies suggest that EMT mediates HNSCC progression. The mechanistic role of the EMT markers that have been associated with HNSCC should be more clearly defined if new anti-HNSCC therapies to block EMT progression are to be developed.

Indexed as

Basement MembraneBiomarkers, TumorCarcinoma, Squamous CellCell AdhesionCell MovementEpithelial CellsEpithelial-Mesenchymal TransitionHead and Neck NeoplasmsHumansMesodermNeoplasm InvasivenessBiomarkers, Tumor

Identifiers

PMID23128109
PMCPMC3545688
OpenAlexW2080261745

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.