Evidence map›Paper›PMID 27789963›Full record

ArticleOncoTargets and therapy2016

hERG1 positivity and Glut-1 negativity identifies high-risk TNM stage I and II colorectal cancer patients, regardless of adjuvant chemotherapy.

Leonardo Muratori, Giulia Petroni, Lorenzo Antonuzzo, Luca Boni, Jessica Iorio, Elena Lastraioli, Gianluca Bartoli, Luca Messerini, Francesco Di Costanzo, Annarosa Arcangeli

Open access · goldAbstract read
In one paragraph

Article in OncoTargets and therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

14 citing papers in PubMed, 22 citations in OpenAlex.

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  14. The combined activation of KBritish journal of cancer · 2018
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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

10 authors at 4 institutions in 1 country.

Leonardo MuratoriDepartment of Experimental and Clinical Medicine, University of Florence.
Giulia PetroniDepartment of Experimental and Clinical Medicine, University of Florence.
Lorenzo AntonuzzoMedical Oncology, Azienda Ospedaliero-Universitaria Careggi, Florence; Department of Medical Biotechnologies, University of Siena, Siena.
Luca BoniClinical Trials Coordinating Center, Istituto Toscano Tumori, Azienda Ospedaliero-Universitaria Careggi, Florence, Italy.
Jessica IorioDepartment of Experimental and Clinical Medicine, University of Florence; Department of Medical Biotechnologies, University of Siena, Siena.
Elena LastraioliDepartment of Experimental and Clinical Medicine, University of Florence.
Gianluca BartoliDepartment of Experimental and Clinical Medicine, University of Florence.
Luca MesseriniDepartment of Experimental and Clinical Medicine, University of Florence.
Francesco Di CostanzoMedical Oncology, Azienda Ospedaliero-Universitaria Careggi, Florence.
Annarosa ArcangeliDepartment of Experimental and Clinical Medicine, University of Florence.
University of Florence · ITAzienda Ospedaliero-Universitaria Careggi · ITAzienda Ospedaliera Universitaria Senese · ITUniversity of Siena · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe identification of early-stage colorectal cancer (CRC) with high risk of progression is one major clinical challenge, mainly due to lack of validated biomarkers. The aims of the present study were to analyze the prognostic impact of three molecular markers belonging to the ion channels and transporters family: the PATIENTS AND

methodsThe expressions of hERG1, KCa3.1, and Glut-1 were tested by immunohistochemistry on 162 surgical samples of nonmetastatic, stage I-III CRC patients. The median follow-up was 32 months. The association between biological markers, clinicopathological features, and survival outcomes was investigated by evaluating both disease-free survival and overall survival.

resultsAlthough no prognostic valence emerged for KCa3.1, evidence of a negative impact of hERG1 expression on survival outcomes was provided. On the contrary, Glut-1 expression had a positive impact. According to the results of the multivariate analysis, patients were stratified in four risk groups, based on TNM stage and hERG1/Glut-1 expression. After adjusting for adjuvant therapy, stage I and II, Glut-1-negative, and hERG1-positive patients showed the worst survival experience.

conclusionThis study strongly indicates that the combination of hERG1 positivity and Glut-1 negativity behaves as a prognostic biomarker in radically resected CRC patients. This combination identifies a group of stage I and II CRC patients with a bad prognosis, even worse than that of stage III patients, regardless of adjuvant therapy accomplishment.

Indexed as

biomolecular markersglucose transporterion channelspotassium channelsprognostic markers

Identifiers

PMID27789963
PMCPMC5072508
OpenAlexW2530131094

What OpenQuestion holds

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Registered trials

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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.