Evidence map›Paper›PMID 35138436›Full record

ArticleWorld journal of urology2022

A study of the immunohistochemical profile of bladder cancer in neuro-urological patients by the French Association of Urology.

Floriane Michel, Fabiana Cancrini, Géraldine Cancel-Tassin, Xavier Gamé, Eric Huyghe, Aurélien Rock, Grégoire Léon, Audrey Uzan, François-Régis Desfemmes, Benoît Peyronnet and 12 more

Abstract read
PubMed Publisher
In one paragraph

Article in World journal of urology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

2 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
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 10 institutions in 3 countries.

Floriane MichelDepartment of Urology and Kidney Transplantation, Aix-Marseille University, La Conception Hospital, Assistance Publique-Hôpitaux de Marseille, 147 Boulevard Baille, 13005, Marseille, France. floriane.michel@ap-hm.fr.ORCID http://orcid.org/0000-0002-5445-4791
Fabiana CancriniSorbonne University, GRC5 Predictive Onco-urology, Assistance Publique-Hôpitaux de Paris, Paris, France.
Géraldine Cancel-TassinSorbonne University, GRC5 Predictive Onco-urology, Assistance Publique-Hôpitaux de Paris, Paris, France.
Xavier GaméDepartment of Urology, CHU Rangueil, Université Paul Sabatier Toulouse III, Toulouse, France.
Eric HuygheDepartment of Urology, CHU Rangueil, Université Paul Sabatier Toulouse III, Toulouse, France.
Aurélien RockDepartment of Urology, Groupe Hospitalier de L'Institut Catholique Lillois, Lille, France.
Grégoire LéonDepartment of Urology and Transplantation, CHU de Caen, Caen, France.
Audrey UzanDepartment of Urology, Sorbonne University, Tenon Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.
François-Régis DesfemmesDepartment of Urology, Hôpital d'instruction Des Armées du Val de Grace, Paris, France.
Benoît PeyronnetDepartment of Urology, University of Rennes, Rennes, France.
Jérémy FallotDepartment of Urology, Royal Prince Alfred Hospital, Sydney, NSW, Australia.
Priscilla LéonDepartment of Urology, Clinique Urologie Royan, Royan, France.
Emmanuel RollandDepartment of Urology, Clinique Toulouse Lautrec, Albi, France.
Marie-Aimée Perrouin-VerbeDepartment of Urology and Transplantation Surgery, Nantes University Hospital, Nantes, France.
Jacques WodeyDepartment of Urology, Clinique Rhône Durance, Avignon, France.
Grégoire CaponDepartment of Urology, University of Bordeaux, Bordeaux, France.
Gilles KarsentyDepartment of Urology and Kidney Transplantation, Aix-Marseille University, La Conception Hospital, Assistance Publique-Hôpitaux de Marseille, 147 Boulevard Baille, 13005, Marseille, France.
Morgan RouprêtSorbonne University, GRC5 Predictive Onco-urology, Assistance Publique-Hôpitaux de Paris, Paris, France.
Olivier CussenotSorbonne University, GRC5 Predictive Onco-urology, Assistance Publique-Hôpitaux de Paris, Paris, France.
Hussa AlshehhiDepartment of Pathology, Sorbonne University, Tenon Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.
Eva ComperatSorbonne University, GRC5 Predictive Onco-urology, Assistance Publique-Hôpitaux de Paris, Paris, France.
Véronique PhéSorbonne University, GRC5 Predictive Onco-urology, Assistance Publique-Hôpitaux de Paris, Paris, France.
Sorbonne Université · FRAix-Marseille Université · FRUniversité Toulouse III - Paul Sabatier · FRCentre Hospitalier Universitaire de Caen Normandie · FRCentre Hospitalier Universitaire de Rennes · FRClinique Pasteur · FRGroupe Hospitalier de l'Institut Catholique de Lille · FRHIA du Val-de-Grâce à Paris · FRRoyal Prince Alfred Hospital · AUUniversité de Bordeaux · FR

Funding

French Association of Urology (Association Française d'Urologie-AFU) Bourse AFU 2020French-speaking Neuro-Urology Study Group (Groupe d'Etude de Neuro-Urologie de Langue Française-GENULF) Bourse GENULF 2020
6 · The paper itself

Abstract

purposeTo establish whether the expression of markers of cell differentiation (CK7, CK14, CK20, GATA3), apoptosis (p53), proliferation (Ki67, STAG2) and peri-tumoural lymphocytes (CD3, CD8), provides specific information about urothelial carcinogenesis in neuro-urological patients with bladder cancer (NBC).

methodsTissue samples from NBC were retrieved from 15 centres in France and compared to control samples from non neuro-urological patients with bladder cancer (NNBC) and from neuro-urological patients without bladder cancer (NB). The expression of CK7, CK14, CK20, GATA3, p53, Ki67, STAG2, CD3 and CD8 markers was analysed using immunohistochemistry of tissue microarray sections.

resultsOverall, tissue samples from 124 patients were included in the study (n = 72 NBC, n = 26 NNBC and n = 26 NB). Muscle invasive bladder cancer (MIBC) was found in 52 NBC patients (72.2%) and squamous cell differentiation in 9 (12.5%). In NBC samples, the expression of CK20 and GATA3 was significantly more frequent in NMIBC compared to MIBC (p = 0.015 and p = 0.004, respectively). CK20 and GATA3 were significantly more expressed in NBC compared to NNBC (p < 0.001 and p = 0.010, respectively). The expression of CK14, Ki67, CD3 and CD8 was significantly more frequent in NBC than in NNBC samples (p = 0.005, p < 0.001, p < 0.001 and p < 0.001, respectively). The expression of CD3 and CD8 was similar in NBC and NB samples.

conclusionIn NBC, markers of basal differentiation, proliferation and peri-tumoural lymphocytes were significantly more expressed compared to NNBC controls. These results suggest the aggressiveness of NBC and the role of chronic inflammation in the carcinogenesis of bladder cancer in neuro-urological patients.

Indexed as

Urinary Bladder NeoplasmsUrologyBiomarkers, TumorCarcinogenesisHumansKi-67 AntigenTumor Suppressor Protein p53Biomarkers, TumorKi-67 AntigenTumor Suppressor Protein p53ImmunohistochemistryInflammationSquamous cell carcinomaUrinary bladder neoplasmsUrinary bladder neurogenic

Identifiers

PMID35138436
OpenAlexW4210928235

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.