Evidence map›Paper›PMID 25026278›Full record

ArticleOncotarget2014

H-Prune through GSK-3β interaction sustains canonical WNT/β-catenin signaling enhancing cancer progression in NSCLC.

Marianeve Carotenuto, Pasqualino De Antonellis, Lucia Liguori, Giovanna Benvenuto, Daniela Magliulo, Alessandro Alonzi, Cecilia Turino, Carmela Attanasio, Valentina Damiani, Anna Maria Bello and 12 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

21 citing papers in PubMed, 48 citations in OpenAlex.

  1. Inorganic Polyphosphate and Human Diseases.Progress in molecular and subcellular biology · 2026
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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

22 authors at 8 institutions in 4 countries.

Marianeve CarotenutoCentro di Ingegneria Genetica e Biotecnologie Avanzate (CEINGE), Naples, Italy; Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università 'Federico II' di Naples, Italy.
Pasqualino De AntonellisCentro di Ingegneria Genetica e Biotecnologie Avanzate (CEINGE), Naples, Italy; Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università 'Federico II' di Naples, Italy.
Lucia LiguoriCentro di Ingegneria Genetica e Biotecnologie Avanzate (CEINGE), Naples, Italy; Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università 'Federico II' di Naples, Italy.
Giovanna BenvenutoStazione Zoologica Anthon Dohrn, Villa Comunale, Naples, Italy.
Daniela MagliuloCentro di Ingegneria Genetica e Biotecnologie Avanzate (CEINGE), Naples, Italy; Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università 'Federico II' di Naples, Italy.
Alessandro AlonziCentro di Ingegneria Genetica e Biotecnologie Avanzate (CEINGE), Naples, Italy; Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università 'Federico II' di Naples, Italy.
Cecilia TurinoDipartimento di Scienze Cardiotoraciche e Respiratorie, Clinica Seconda Università degli Studi di Napoli, Naples, Italy.
Carmela AttanasioCentro di Ingegneria Genetica e Biotecnologie Avanzate (CEINGE), Naples, Italy; Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università 'Federico II' di Naples, Italy.
Valentina DamianiCentro di Ingegneria Genetica e Biotecnologie Avanzate (CEINGE), Naples, Italy; Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università 'Federico II' di Naples, Italy.
Anna Maria BelloCentro di Ingegneria Genetica e Biotecnologie Avanzate (CEINGE), Naples, Italy; Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università 'Federico II' di Naples, Italy.
Fabiana VitielloDipartimento di Pneumologia e Tisiologia, Day Hospital Pneumologia e Pneumoncologico, AORN Vincenzo Monaldi, Naples, Italy.
Rosa PasquinelliFunctional Genomic Unit, National Cancer Institute, Fondazione G. Pascale, Naples, Italy.
Luigi TerraccianoInstitute of Pathology, Molecular Pathology Division, University of Basel, Switzerland.
Antonella FedericoDipartimento di Biologia e Patologia Cellulare e Molecolare, Istituto Di Endocrinologia e Oncologia Sperimentale del CNR, Naples, Italy.
Alfredo FuscoDipartimento di Biologia e Patologia Cellulare e Molecolare, Istituto Di Endocrinologia e Oncologia Sperimentale del CNR, Naples, Italy.
Jamie FreemanSchool of Biosciences, Cardiff University, Museum Avenue, Cardiff, Wales, UK.
Trevor C DaleSchool of Biosciences, Cardiff University, Museum Avenue, Cardiff, Wales, UK.
Charles DecraeneTranslational Research Dept, Institut Curie, Centre de recherche, Paris, France; CNRS, UMR144, Paris, France.
Gennaro ChiappettaFunctional Genomic Unit, National Cancer Institute, Fondazione G. Pascale, Naples, Italy.
Francovito PiantedosiDipartimento di Pneumologia e Tisiologia, Day Hospital Pneumologia e Pneumoncologico, AORN Vincenzo Monaldi, Naples, Italy.
Cecilia CalabreseDipartimento di Scienze Cardiotoraciche e Respiratorie, Clinica Seconda Università degli Studi di Napoli, Naples, Italy.
Massimo ZolloCentro di Ingegneria Genetica e Biotecnologie Avanzate (CEINGE), Naples, Italy; Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università 'Federico II' di Naples, Italy; Azienda Ospedaliera Federico II, DAI Medicina Trasfusionale Virologia, Naples, Italy.
University of Naples Federico II · ITCardiff University · GBInstitute for Experimental Endocrinology and Oncology · ITIstituto Nazionale Tumori IRCCS "Fondazione G. Pascale" · ITOspedale Monaldi · ITCentre National de la Recherche Scientifique · FRStazione Zoologica Anton Dohrn · ITUniversity of Basel · CH

Funding

Biotechnology and Biological Sciences Research Council BB/D00117X/1Cancer Research UK 15937
6 · The paper itself

Abstract

H-Prune hydrolyzes short-chain polyphosphates (PPase activity) together with an hitherto cAMP-phosphodiesterase (PDE), the latest influencing different human cancers by its overexpression. H-Prune promotes cell migration in cooperation with glycogen synthase kinase-3 (Gsk-3β). Gsk-3β is a negative regulator of canonical WNT/β-catenin signaling. Here, we investigate the role of Gsk-3β/h-Prune complex in the regulation of WNT/β-catenin signaling, demonstrating the h-Prune capability to activate WNT signaling also in a paracrine manner, through Wnt3a secretion. In vivo study demonstrates that h-Prune silencing inhibits lung metastasis formation, increasing mouse survival. We assessed h-Prune levels in peripheral blood of lung cancer patients using ELISA assay, showing that h-Prune is an early diagnostic marker for lung cancer. Our study dissects out the mechanism of action of h-Prune in tumorigenic cells and also sheds light on the identification of a new therapeutic target in non-small-cell lung cancer.

Indexed as

Wnt Signaling PathwayAnimalsbeta CateninCarcinoma, Non-Small-Cell LungCarrier ProteinsDisease ProgressionFemaleGlycogen Synthase Kinase 3Glycogen Synthase Kinase 3 betaHeterograftsHumansLung NeoplasmsMiceMice, NudePhosphoric Monoester Hydrolasesbeta CateninCarrier ProteinsCTNNB1 protein, humanGlycogen Synthase Kinase 3Glycogen Synthase Kinase 3 betaGSK3B protein, humanGsk3b protein, mousePhosphoric Monoester HydrolasesPRUNE1 protein, human

Identifiers

PMID25026278
PMCPMC4170634
OpenAlexW1922027332

What OpenQuestion holds

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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.