Evidence map›Paper›PMID 30650148›Full record

ArticlePloS one2019

Molecular characterization of low grade and high grade bladder cancer.

Alessandro Apollo, Valerio Ortenzi, Cristian Scatena, Katia Zavaglia, Paolo Aretini, Francesca Lessi, Sara Franceschi, Sara Tomei, Carlo Alberto Sepich, Paolo Viacava and 2 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04872036 (Investigation of Prognostic Biomarkers in Patients With Urothelial Carcinoma Treated With Platinum Regimens), which is not on this map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.7field-weighted citation impact, top 11% 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.

NCT04872036 completednot on this map

Investigation of Prognostic Biomarkers in Patients With Urothelial Carcinoma Treated With Platinum Regimens

TypeobservationalSponsorHellenic Cooperative Oncology GroupRan2000 to 2017Enrolled66ConditionsBladder Cancer
3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
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  7. Review
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  10. Biomarkers and intermediate-high risk non-muscle invasive bladder cancer: a multivariate analysis of three different cellular pathways with pronostic implications.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2021
    Observational
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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 5 institutions in 1 country.

Alessandro ApolloGenetic Unit of Biology Department, University of Pisa, Pisa, Italy.ORCID 0000-0002-4134-0314
Valerio OrtenziDepartment of Pathology, University Hospital of Pisa, Pisa, Italy.
Cristian ScatenaDepartment of Pathology, University Hospital of Pisa, Pisa, Italy.
Katia ZavagliaDepartment of Pathology, University Hospital of Pisa, Pisa, Italy.
Paolo AretiniSection of Cancer Genomics, Fondazione Pisana per la Scienza, Pisa, Italy.
Francesca LessiSection of Cancer Genomics, Fondazione Pisana per la Scienza, Pisa, Italy.
Sara FranceschiSection of Cancer Genomics, Fondazione Pisana per la Scienza, Pisa, Italy.
Sara TomeiOmics Core and Biorepository, Sidra Medicine, Doha, Qatar.
Carlo Alberto SepichDivision of Urology, Versilia Hospital, Lido di Camaiore, Italy.
Paolo ViacavaDivision of Pathology, Hospital of Livorno, Livorno, Italy.
Chiara Maria MazzantiSection of Cancer Genomics, Fondazione Pisana per la Scienza, Pisa, Italy.
Antonio Giuseppe NaccaratoDepartment of Pathology, University Hospital of Pisa, Pisa, Italy.
Azienda Ospedaliera Universitaria Pisana · ITFondazione Pisa · ITOspedale di Livorno · ITOspedale Versilia · ITUniversity of Pisa · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBladder cancer (BC) is the 9th most common cancer diagnosis worldwide. Low grade (LG) represents 70% of all BCs, characterized by recurrence and rare ability (10-15%) to progress to high grade (HG) and invade. The remaining 30% is high grade (HG), fast invasive BC, which is resistant to therapy. Identifying biomarkers for predicting those tumors able to progress is a key goal for patient outcome improvement. This study focuses on the most promising prognostic markers. MATERIALS AND

methodsTP53 and FGFR3 mutational status, Survivin, CK19, CK20, E-cadherin and CD44 gene expression analysis were performed on 66 BCs.

resultsSurvivin was found associated to tumor grade (p<0.05). Moreover, Survivin correlated with CD44 in TP53 wild type (p = 0.0242) and FGFR3 wild type (p = 0.0036) tumors. In particular the Survivin-CD44 correlation was associated to HG FGFR3 wild type BCs (p = 0.0045). Unsupervised hierarchical clustering based on gene expression data identified four distinct molecular groups reflecting the patient histology (p = 0.038).

conclusionWe suggest Survivin, both as a biomarker associated to G3 BCs but negatively related to TP53 mutational status, and as a potential novel therapeutic target.

Indexed as

AgedCadherinsDNA Mutational AnalysisFemaleHumansHyaluronan ReceptorsKeratin-20MaleMutationNeoplasm GradingReceptor, Fibroblast Growth Factor, Type 3SurvivinTumor Suppressor Protein p53Urinary BladderUrinary Bladder NeoplasmsCadherinsFGFR3 protein, humanHyaluronan ReceptorsKeratin-20KRT20 protein, humanReceptor, Fibroblast Growth Factor, Type 3SurvivinTumor Suppressor Protein p53

Identifiers

PMID30650148
PMCPMC6334926
OpenAlexW2908859065

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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.