Evidence map›Paper›PMID 24893613›Full record

ArticleJournal of experimental & clinical cancer research : CR2014

Urotensin II receptor determines prognosis of bladder cancer regulating cell motility/invasion.

Renato Franco, Silvia Zappavigna, Vincenzo Gigantino, Amalia Luce, Monica Cantile, Margherita Cerrone, Gaetano Facchini, Sisto Perdonà, Sandro Pignata, Giuseppe Di Lorenzo and 9 more

Open access · goldAbstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
4.7field-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

17 citing papers in PubMed, 27 citations in OpenAlex.

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  12. Obesity and brain illness: from cognitive and psychological evidences to obesity paradox.Diabetes, metabolic syndrome and obesity : targets and therapy · 2017
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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

19 authors at 5 institutions in 1 country.

Renato Franco
Silvia Zappavigna
Vincenzo Gigantino
Amalia Luce
Monica Cantile
Margherita Cerrone
Gaetano Facchini
Sisto Perdonà
Sandro Pignata
Giuseppe Di Lorenzo
Sergio Chieffi
Giovanni Vitale
Marco De Sio
Alessandro Sgambato
Gerardo Botti
Ali Munaim Yousif
Ettore Novellino
Paolo Grieco
Michele CaragliaDepartment of Biochemistry, Biophysics and General Pathology, Second University of Naples, Naples, Italy. michele.caraglia@unina2.it.
Istituto Nazionale Tumori IRCCS "Fondazione G. Pascale" · ITUniversity of Naples Federico II · ITUniversity of Campania "Luigi Vanvitelli" · ITFederico II University Hospital · ITIRCCS Istituto Auxologico Italiano · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNon Muscle Invasive Bladder Transitional Cancer (NMIBC) and Muscle Invasive Bladder Transitional Cancer (MIBC)/invasive have different gene profile and clinical course. NMIBC prognosis is not completely predictable, since the relapse rate is higher than 20%, even in the form of MIBC. The aim of this study is to evaluate if UTR expression can discriminate between NMIBC and MIBC and predict the risk of relapses in NMIBCs.

methodsWe have investigated upon urotensin-II (UII) receptor (UTR) expression in vivo in 159 patients affected by NMIBC. The biological role of UTR was also investigated in vitro. UTR expression was evaluated in a tissue-micro-array, consisting of normal, NMIBC and invasive bTCC samples.

resultsUTR discriminated between NMIBC and MIBC and showed a significant correlation between low UTR expression and shorter disease free survival in NMIBC. The superagonist UPG84 induced growth suppression at nM concentrations on 3/4 cell lines. Bladder cancer cell treatment with the antagonist urantide or the knock-down of UTR with a specific shRNA significantly blocked both the motility and invasion of bladder cancer cells.

conclusionsThe evaluation of UTR expression can discriminate between NMIBC at high and low risk of relapse. Moreover, our data suggest that UTR is involved in the regulation of motility, invasion and proliferation of bladder cancer cells. High UTR expression is an independent prognostic factor of good prognosis for NMIBC regulating motility and invasion of bladder cancer cells.

Indexed as

Cell MovementAdultAgedAged, 80 and overCarcinoma, Transitional CellCell Line, TumorCell ProliferationDisease-Free SurvivalFemaleGene ExpressionHumansKaplan-Meier EstimateMaleMiddle AgedNeoplasm InvasivenessNeoplasm Recurrence, LocalPeptide FragmentsReceptors, G-Protein-Coupledurotensin IIurotensin II (4-11), Pen(5)-Trp(7)-Orn(8)-UrotensinsUTS2R protein, human

Identifiers

PMID24893613
PMCPMC4061920
OpenAlexW2143347215

What OpenQuestion holds

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LicenceCC BY
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.