Evidence map›Paper›PMID 33543019›Full record

ArticleMatrix biology plus2020

Loss of Tenascin-X expression during tumor progression: A new pan-cancer marker.

Sophie Liot, Alexandre Aubert, Valérie Hervieu, Naïma El Kholti, Joost Schalkwijk, Bernard Verrier, Ulrich Valcourt, Elise Lambert

Open access · goldAbstract read
In one paragraph

Article in Matrix biology plus, 2020. 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
4.2field-weighted citation impact, top 5% 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, 47 citations in OpenAlex.

  1. Article
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  4. UnravelingInternational journal of molecular sciences · 2025
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  11. Expression profiling of luminal B breast tumor in Indian women.Journal of cancer research and clinical oncology · 2023
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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

8 authors at 5 institutions in 2 countries.

Sophie LiotLaboratoire de Biologie Tissulaire et Ingénierie Thérapeutique (LBTI), UMR CNRS 5305, Université Lyon 1, Institut de Biologie et Chimie des Protéines, 7, passage du Vercors, F-69367 Lyon Cedex 07, France.
Alexandre AubertLaboratoire de Biologie Tissulaire et Ingénierie Thérapeutique (LBTI), UMR CNRS 5305, Université Lyon 1, Institut de Biologie et Chimie des Protéines, 7, passage du Vercors, F-69367 Lyon Cedex 07, France.
Valérie HervieuService d'Anatomopathologie, Groupement Hospitalier Est, Hospices Civils de Lyon, Lyon, France.
Naïma El KholtiLaboratoire de Biologie Tissulaire et Ingénierie Thérapeutique (LBTI), UMR CNRS 5305, Université Lyon 1, Institut de Biologie et Chimie des Protéines, 7, passage du Vercors, F-69367 Lyon Cedex 07, France.
Joost SchalkwijkRadboud Institute for Molecular Life Sciences, Faculty of Medical Sciences, 370 Geert Grooteplein-Zuid 26 28, 6525 GA Nijmegen, Netherlands.
Bernard VerrierLaboratoire de Biologie Tissulaire et Ingénierie Thérapeutique (LBTI), UMR CNRS 5305, Université Lyon 1, Institut de Biologie et Chimie des Protéines, 7, passage du Vercors, F-69367 Lyon Cedex 07, France.
Ulrich ValcourtLaboratoire de Biologie Tissulaire et Ingénierie Thérapeutique (LBTI), UMR CNRS 5305, Université Lyon 1, Institut de Biologie et Chimie des Protéines, 7, passage du Vercors, F-69367 Lyon Cedex 07, France.
Elise LambertLaboratoire de Biologie Tissulaire et Ingénierie Thérapeutique (LBTI), UMR CNRS 5305, Université Lyon 1, Institut de Biologie et Chimie des Protéines, 7, passage du Vercors, F-69367 Lyon Cedex 07, France.
Université Claude Bernard Lyon 1 · FRCentre National de la Recherche Scientifique · FRBiologie Tissulaire et Ingénierie Thérapeutique · FRHospices Civils de Lyon · FRRadboud University Nijmegen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer is a systemic disease involving multiple components produced from both tumor cells themselves and surrounding stromal cells. The pro- or anti-tumoral role of the stroma is still under debate. Indeed, it has long been considered the main physical barrier to the diffusion of chemotherapy by its dense and fibrous nature and its poor vascularization. However, in murine models, the depletion of fibroblasts, the main ExtraCellular Matrix (ECM)-producing cells, led to more aggressive tumors even though they were more susceptible to anti-angiogenic and immuno-modulators. Tenascin-C (TNC) is a multifunctional matricellular glycoprotein (

Indexed as

CAF, Cancer-Associated FibroblastCancersD.E.G., Differentially Expressed GenesECM, Extracellular MatrixEDS, Ehlers-Danlos syndromeFBG, fibrinogenFNIII, fibronectin type IIIGEO, Gene Expression OmnibusGSE, GEO SeriesHDAC1, histone deacetylase-1lncRNA, long non-coding RNAMeta-analysisMMP, Matrix MetalloproteinaseMPNST, Malignant Peripheral Nerve Sheath TumorsmRNA and protein levelsPrognosis markerTCGA, The Cancer Genome AtlasTenascin-XTissue MicroArrayTMA, Tissue MicroArrayTME, Tumor MicroEnvironmentTNC, Tenascin-CTNR, Tenascin-RTN, TenascinTNW, Tenascin-WTNX, Tenascin-XTSS, Transcription Start Site

Identifiers

PMID33543019
PMCPMC7852205
OpenAlexW3001815398

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.