Evidence map›Paper›PMID 31807018›Full record

ArticleOncoTargets and therapy2019

The hERG1 Potassium Channel Behaves As Prognostic Factor In Gastric Dysplasia Endoscopic Samples.

Elena Lastraioli, Maria Raffaella Romoli, Jessica Iorio, Tiziano Lottini, Mariella Chiudinelli, Maria Bencivenga, Carla Vindigni, Anna Tomezzoli, Giovanni De Manzoni, Bruno Compagnoni and 5 more

Open access · goldAbstract read
In one paragraph

Article in OncoTargets and therapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 40% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
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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

15 authors at 6 institutions in 1 country.

Elena LastraioliDepartment of Experimental and Clinical Medicine, Section of Internal Medicine, University Of Florence, Florence 50134, Italy.ORCID 0000-0002-1531-8973
Maria Raffaella RomoliDepartment of Experimental and Clinical Medicine, Section of Internal Medicine, University Of Florence, Florence 50134, Italy.
Jessica IorioDepartment of Experimental and Clinical Medicine, Section of Internal Medicine, University Of Florence, Florence 50134, Italy.
Tiziano LottiniDepartment of Experimental and Clinical Medicine, Section of Internal Medicine, University Of Florence, Florence 50134, Italy.
Mariella ChiudinelliPathology Division, Esine Hospital, ASST della Valcamonica, Esine, BS 25040, Italy.ORCID 0000-0001-5937-3889
Maria BencivengaSurgery Division, University of Verona, Verona 37134, Italy.
Carla VindigniPathology Division, Azienda Ospedaliero-Universitaria Senese, Siena 53100, Italy.ORCID 0000-0001-9624-2300
Anna TomezzoliPathology Division, Borgo Trento Hospital, Verona 37134, Italy.
Giovanni De ManzoniSurgery Division, University of Verona, Verona 37134, Italy.
Bruno CompagnoniSurgery Division, Esine Hospital, ASST della Valcamonica, Esine, BS 25040, Italy.
Ilaria ManziGastroenterology and Endoscopy Unit, Morgagni-Pierantoni Hospital, Forlì 47121, Italy.
Luca MesseriniDepartment of Experimental and Clinical Medicine, Section of Internal Medicine, University Of Florence, Florence 50134, Italy.
Luca SaragoniPathology Division, Morgagni-Pierantoni Hospital, Forlì 47121, Italy.
Annarosa ArcangeliDepartment of Experimental and Clinical Medicine, Section of Internal Medicine, University Of Florence, Florence 50134, Italy.
Gruppo Italiano di Ricerca Cancro Gastrico (GIRCG)
University of Florence · ITAziende Socio Sanitarie Territoriale della ValcamonicaOspedale G.B. Morgagni - L.Pierantoni · ITUniversity of Verona · ITAzienda Ospedaliera Universitaria Senese · ITProvincia Autonoma di Trento · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeGastric cancer (GC) is still a relevant health issue worldwide. The identification of prognostic factors for progression of gastric dysplasia (GD), the main pre-cancerous lesion of the intestinal-type GC, is hence mandatory. PATIENTS AND

methodsA cohort of 83 GD endoscopic samples belonging to Italian subjects was collected. hERG1 expression was evaluated by immunohistochemistry and scored 0-3, depending on the percentage of stained cells. Expression data were analysed in conjunction with clinico-pathological and survival data.

resultshERG1 turned out to be expressed in 67.47% (56 out of 83) of the GD samples. hERG1 expression was higher in high-grade GD compared to low-grade GD (29 out of 39, 74.36% vs 27 out of 44, 61.36%), although the statistical significance was not reached (P=0.246). No association emerged between hERG1 expression and clinical features of the patients (age, gender, localization,

conclusionhERG1 is aberrantly expressed in human GD samples and has an impact on both PFS and OS, hence representing a novel prognostic marker for progression of GD towards GC of the intestinal histotype. Once properly validated, hERG1 detection could be included in the clinical practice, during endoscopic surveillance protocols, for the management of GD at higher risk of progression, as already proposed for Barrett's oesophagus.

Indexed as

endoscopic surveillance in gastric dysplasiaimmunohistochemistryintestinal type gastric adenocarcinomaKv11.1prognosis

Identifiers

PMID31807018
PMCPMC6844225
OpenAlexW2988779525

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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.