Evidence map›Paper›PMID 23559515›Full record

ArticleJournal of molecular cell biology2013

NG2/CSPG4-collagen type VI interplays putatively involved in the microenvironmental control of tumour engraftment and local expansion.

Sabrina Cattaruzza, Pier Andrea Nicolosi, Paola Braghetta, Laura Pazzaglia, Maria Serena Benassi, Piero Picci, Katia Lacrima, Daniela Zanocco, Erika Rizzo, William B Stallcup and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of molecular cell biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
4.3field-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

45 citing papers in PubMed, 64 citations in OpenAlex.

  1. Review
  2. NG2 Glia and Cellular Crosstalk in Health and Disease: Focus on Spinal Cord Injury.Pathophysiology : the official journal of the International Society for Pathophysiology · 2026
    Review
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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

12 authors at 6 institutions in 2 countries.

Sabrina CattaruzzaSOS for Experimental Oncology 2, The National Tumour Institute Aviano-CRO-IRCCS, Aviano (PN), Italy.
Pier Andrea Nicolosi
Paola Braghetta
Laura Pazzaglia
Maria Serena Benassi
Piero Picci
Katia Lacrima
Daniela Zanocco
Erika Rizzo
William B Stallcup
Alfonso Colombatti
Roberto Perris
Istituti di Ricovero e Cura a Carattere Scientifico · ITIstituto Ortopedico Rizzoli · ITCentro di Riferimento Oncologico · ITUniversity of Padua · ITSanford Burnham Prebys Medical Discovery Institute · USUniversity of Parma · IT

Funding

NG2-PG in tumor vascularization and progressionR01CA095287 · NCI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI STALLCUP, WILLIAM B. · 2002 to 2016
$5.3M
NCI NIH HHS R01 CA095287
6 · The paper itself

Abstract

In soft-tissue sarcoma patients, enhanced expression of NG2/CSPG4 proteoglycan in pre-surgical primary tumours predicts post-surgical metastasis formation and thereby stratifies patients into disease-free survivors and patients destined to succumb to the disease. Both primary and secondary sarcoma lesions also up-regulate collagen type VI, a putative extracellular matrix ligand of NG2, and this matrix alteration potentiates the prognostic impact of NG2. Enhanced constitutive levels of the proteoglycan in isolated sarcoma cells closely correlate with a superior engraftment capability and local growth in xenogenic settings. This apparent NG2-associated malignancy was also corroborated by the diverse tumorigenic behaviour in vitro and in vivo of immunoselected NG2-expressing and NG2-deficient cell subsets, by RNAi-mediated knock down of endogenous NG2, and by ectopic transduction of full-length or deletion constructs of NG2. Cells with modified expression of NG2 diverged in their interaction with purified Col VI, matrices supplemented with Col VI, and cell-free matrices isolated from wild-type and Col VI null fibroblasts. The combined use of dominant-negative NG2 mutant cells and purified domain fragments of the collagen allowed us to pinpoint the reciprocal binding sites within the two molecules and to assert the importance of this molecular interaction in the control of sarcoma cell adhesion and motility. The NG2-mediated binding to Col VI triggered activation of convergent cell survival- and cell adhesion/migration-promoting signal transduction pathways, implicating PI-3K as a common denominator. Thus, the findings point to an NG2-Col VI interplay as putatively involved in the regulation of the cancer cell-host microenvironment interactions sustaining sarcoma progression.

Indexed as

AdultAgedAnimalsCell Line, TumorCell MovementChondroitin Sulfate Proteoglycan 4Chondroitin Sulfate ProteoglycansCollagen Type VIHumansMelanoma, ExperimentalMembrane ProteinsMiceMiddle AgedRNA InterferenceSarcomaSignal TransductionChondroitin Sulfate Proteoglycan 4Chondroitin Sulfate ProteoglycansCollagen Type VICSPG4 protein, humanMembrane Proteinscell migrationcollagen type VIprognostic biomarkerproteoglycanssarcomatumour–stroma interaction

Identifiers

PMID23559515
PMCPMC3656611
OpenAlexW2168480575

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.