Evidence map›Paper›PMID 25767619›Full record

ReviewTheranostics2015

Theranostic impact of NG2/CSPG4 proteoglycan in cancer.

Pier Andrea Nicolosi, Alice Dallatomasina, Roberto Perris

Open access · goldAbstract readReview
In one paragraph

Review in Theranostics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

52 citing papers in PubMed, 77 citations in OpenAlex.

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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

3 authors at 2 institutions in 1 country.

Pier Andrea Nicolosi1. Department of Experimental Oncology 2, National Tumour Institute Aviano, CRO-IRCCS, Via Franco Gallini 2, 33081 AVIANO (PN), Italy;
Alice Dallatomasina2. COMT - Centre for Molecular and Translational Oncology;
Roberto Perris1. Department of Experimental Oncology 2, National Tumour Institute Aviano, CRO-IRCCS, Via Franco Gallini 2, 33081 AVIANO (PN), Italy; ; 2. COMT - Centre for Molecular and Translational Oncology; ; 3. Department of Life Sciences, University of Parma, Parco Area delle Scienze 11/A, 43124 PARMA, Italy.
Istituti di Ricovero e Cura a Carattere Scientifico · ITUniversity of Parma · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

NG2/CSPG4 is an unusual cell-membrane integral proteoglycan widely recognized to be a prognostic factor, a valuable tool for ex vivo and non-invasive molecular diagnostics and, by virtue of its tight association with malignancy, a tantalizing therapeutic target in several tumour types. Although the biology behind its involvement in cancer progression needs to be better understood, implementation of NG2/CSPG4 in the routine clinical practice is attainable and has the potential to contribute to an improved individualized management of cancer patients. In this context, its polymorphic nature seems to be particularly valuable in the effort to standardize informative diagnostic procedures and consolidate forcible immunotherapeutic treatment strategies. We discuss here the underpinnings for this potential and highlight the benefits of taking advantage of the intra-tumour and inter-patient variability in the regulation of NG2/CSPG4 expression. We envision that NG2/CSPG4 may effectively be exploited in therapeutic interventions aimed at averting resistance to target therapy agents and at interfering with secondary lesion formation and/or tumour recurrence.

Indexed as

AntigensChondroitin Sulfate Proteoglycan 4Diagnostic Tests, RoutineHumansImmunotherapyNeoplasmsProteoglycansAntigensChondroitin Sulfate Proteoglycan 4ProteoglycanscancerCSPG4NG2proteoglycan

Identifiers

PMID25767619
PMCPMC4350014
OpenAlexW2089586958

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.