Evidence map›Paper›PMID 29719622›Full record

ArticleOncotarget2018

Glucose transporter 1 expression as a marker of prognosis in oesophageal adenocarcinoma.

Jaine K Blayney, Lauren Cairns, Gerald Li, Niamh McCabe, Leanne Stevenson, Christopher J Peters, Nathan B Reid, Veronica J Spence, Chintapuza Chisambo, Damian McManus and 15 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

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  5. GLUT1 expression in high-risk prostate cancer: correlation withProstate cancer and prostatic diseases · 2020
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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

25 authors at 7 institutions in 1 country.

Jaine K Blayney *Centre for Cancer Research and Cell Biology, Queen's University Belfast, Belfast, Northern Ireland, UK.
Lauren Cairns *Centre for Cancer Research and Cell Biology, Queen's University Belfast, Belfast, Northern Ireland, UK.
Gerald LiCentre for Cancer Research and Cell Biology, Queen's University Belfast, Belfast, Northern Ireland, UK.
Niamh McCabeCentre for Cancer Research and Cell Biology, Queen's University Belfast, Belfast, Northern Ireland, UK.
Leanne StevensonCentre for Cancer Research and Cell Biology, Queen's University Belfast, Belfast, Northern Ireland, UK.
Christopher J PetersDepartment of Surgery and Cancer, Imperial College, London, UK.
Nathan B ReidCentre for Cancer Research and Cell Biology, Queen's University Belfast, Belfast, Northern Ireland, UK.
Veronica J SpenceCentre for Cancer Research and Cell Biology, Queen's University Belfast, Belfast, Northern Ireland, UK.
Chintapuza ChisamboCentre for Cancer Research and Cell Biology, Queen's University Belfast, Belfast, Northern Ireland, UK.
Damian McManusNorthern Ireland Molecular Pathology Laboratory, Centre for Cancer Research and Cell Biology, Queen's University Belfast, Belfast, Northern Ireland, UK.
Jacqueline JamesNorthern Ireland Molecular Pathology Laboratory, Centre for Cancer Research and Cell Biology, Queen's University Belfast, Belfast, Northern Ireland, UK.
Stephen McQuaidNorthern Ireland Molecular Pathology Laboratory, Centre for Cancer Research and Cell Biology, Queen's University Belfast, Belfast, Northern Ireland, UK.
Stephanie CraigNorthern Ireland Molecular Pathology Laboratory, Centre for Cancer Research and Cell Biology, Queen's University Belfast, Belfast, Northern Ireland, UK.
Kenneth ArthurNorthern Ireland Molecular Pathology Laboratory, Centre for Cancer Research and Cell Biology, Queen's University Belfast, Belfast, Northern Ireland, UK.
Darragh McArtCentre for Cancer Research and Cell Biology, Queen's University Belfast, Belfast, Northern Ireland, UK.
Chin-Ann J OngHutchison/MRC Cancer Unit, University of Cambridge, Cambridge, UK.
Pierre Lao-SirieixHutchison/MRC Cancer Unit, University of Cambridge, Cambridge, UK.
Peter HamiltonCentre for Cancer Research and Cell Biology, Queen's University Belfast, Belfast, Northern Ireland, UK.
Manuel Salto-TellezNorthern Ireland Molecular Pathology Laboratory, Centre for Cancer Research and Cell Biology, Queen's University Belfast, Belfast, Northern Ireland, UK.
Martin EatockNorthern Ireland Cancer Centre, Belfast City Hospital, Lisburn Road, Belfast, Northern Ireland, UK.
Helen G ColemanCentre for Public Health, Queen's University Belfast, Belfast, Northern Ireland, UK.
Rebecca C FitzgeraldHutchison/MRC Cancer Unit, University of Cambridge, Cambridge, UK.
Richard D KennedyCentre for Cancer Research and Cell Biology, Queen's University Belfast, Belfast, Northern Ireland, UK.
Richard C TurkingtonCentre for Cancer Research and Cell Biology, Queen's University Belfast, Belfast, Northern Ireland, UK.
Oesophageal Cancer Clinical and Molecular Stratification (OCCAMS) Study Group
Queen's University Belfast · GBThe Northern Ireland Cancer Centre · GBBelfast City Hospital · GBHutchison/MRC Research Centre · GBImperial College London · GBMRC Cancer Unit · GBUniversity of Cambridge · GB

Funding

Cancer Research UK 15874Cancer Research UK 20406Cancer Research UK 25820Medical Research Council MC_UU_12022/2
6 · The paper itself

Abstract

backgroundThe current TNM staging system for oesophageal adenocarcinoma (OAC) has limited ability to stratify patients and inform clinical management following neo-adjuvant chemotherapy and surgery.

resultsFunctional genomic analysis of the gene expression data using Gene Set Enrichment Analysis (GSEA) identified GLUT1 as putative prognostic marker in OAC.In the discovery cohort GLUT1 positivity was observed in 114 patients (80.9%) and was associated with poor overall survival (HR 2.08, 95% CI 1.1-3.94; p=0.024) following multivariate analysis. A prognostic model incorporating GLUT1, CRM and nodal status stratified patients into good, intermediate and poor prognosis groups (p< 0.001) with a median overall survival of 16.6 months in the poorest group.In the validation set 182 patients (69.5%) were GLUT1 positive and the prognostic model separated patients treated with neo-adjuvant chemotherapy and surgery (p<0.001) and surgery alone (p<0.001) into three prognostic groups. PATIENTS AND

methodsTranscriptional profiling of 60 formalin fixed paraffin-embedded (FFPE) biopsies was performed. GLUT1 immunohistochemical staining was assessed in a discovery cohort of 141 FFPE OAC samples treated with neo-adjuvant chemotherapy and surgery at the Northern Ireland Cancer Centre from 2004-2012. Validation was performed in 262 oesophageal adenocarcinomas collected at four OCCAMS consortium centres. The relationship between GLUT1 staining, T stage, N stage, lymphovascular invasion and circumferential resection margin (CRM) status was assessed and a prognostic model developed using Cox Proportional Hazards.

conclusionsGLUT1 staining combined with CRM and nodal status identifies a poor prognosis sub-group of OAC patients and is a novel prognostic marker following potentially curative surgical resection.

Indexed as

biomarkerglucose transporter 1hypoxiaoesophageal cancerprognostic

Identifiers

PMID29719622
PMCPMC5915089
OpenAlexW2792806397

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.