Evidence map›Paper›PMID 32675198›Full record

ArticleBMJ open gastroenterology2020

Infiltrative tumour growth pattern correlates with poor outcome in oesophageal cancer.

Maelle Anciaux, Pieter Demetter, Roland De Wind, Maria Gomez Galdon, Sylvie Vande Velde, Gaspard Lens, Ligia Craciun, Amélie Deleruelle, Denis Larsimont, Tom Lenaerts and 5 more

Abstract read
In one paragraph

Article in BMJ open gastroenterology, 2020. 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
–field-weighted citation impact
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.

  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

15 authors.

Maelle AnciauxDigestive Oncology Laboratory, Institut Jules Bordet, Bruxelles, Belgium.ORCID 0000-0001-7801-5171
Pieter DemetterDepartment of Pathology, Institut Jules Bordet, Bruxelles, Belgium.ORCID 0000-0001-7981-4645
Roland De WindDepartment of Pathology, Institut Jules Bordet, Bruxelles, Belgium.ORCID 0000-0001-8476-1541
Maria Gomez GaldonDepartment of Pathology, Institut Jules Bordet, Bruxelles, Belgium.ORCID 0000-0001-6943-0402
Sylvie Vande VeldeMachine Learning Group, ULB, Bruxelles, Belgium.
Gaspard LensComputer Science Unit, Haute Ecole Leonard de Vinci Institut Paul Lambin, Bruxelles, Belgium.
Ligia CraciunDepartment of Pathology, Institut Jules Bordet, Bruxelles, Belgium.ORCID 0000-0001-6540-8232
Amélie DeleruelleDigestive Oncology Laboratory, Institut Jules Bordet, Bruxelles, Belgium.
Denis LarsimontDepartment of Pathology, Institut Jules Bordet, Bruxelles, Belgium.ORCID 0000-0003-2152-253X
Tom LenaertsMachine Learning Group, ULB, Bruxelles, Belgium.ORCID 0000-0003-3645-1455
Francesco SclafaniDigestive Oncology Laboratory, Institut Jules Bordet, Bruxelles, Belgium.ORCID 0000-0003-0251-2627
Amélie DeleporteGastrointestinal Oncology Unit, Medical Oncology, Institut Jules Bordet, Bruxelles, Belgium.ORCID 0000-0001-6694-0116
Vincent DonckierDepartment of Surgery, Institut Jules Bordet, Bruxelles, Belgium.ORCID 0000-0003-1457-2520
Alain Hendlisz *Gastrointestinal Oncology Unit, Medical Oncology, Institut Jules Bordet, Bruxelles, Belgium alain.hendlisz@bordet.be.ORCID 0000-0003-2122-1948
Caroline Vandeputte *Digestive Oncology Laboratory, Institut Jules Bordet, Bruxelles, Belgium.ORCID 0000-0001-7990-8692

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveOesophageal cancer (OEC) is an aggressive disease with a poor survival rate. Prognostic markers are thus urgently needed. Due to the demonstrated prognostic value of histopathological growth pattern (HGP) in other cancers, we performed a retrospective assessment of HGP in patients suffering from invasive OEC.

designA first cohort composed of 89 treatment-naïve operated patients with OEC from The Cancer Genome Atlas (TCGA) public database was constituted, from which H&E images and RNA-sequencing data were retrieved. Next, a second cohort composed of 99 patients with OEC treated and operated in a Belgian hospital was established. H&E-stained sections and extracted tumorous RNA were obtained from the samples. HGP were assessed on H&E slides as infiltrative (IGP) or expansive (EGP). TCGA RNA-sequencing data were analysed through the gene set enrichment analysis and Cytoscape softwares. Real-time quantitative PCR (qPCR) experiments were performed to assess gene expression in the Belgian cohort.

resultsIGP patients displayed a grim prognosis compared with EGP patients, while IGP was found as associated with numerous lymphovascular emboli and perinervous infiltrations. Analyses of the TCGA expression data showed that angiogenesis, epithelial-to-mesenchymal transition (EMT) and inflammation were significantly upregulated in IGP compared with EGP samples. qPCR experiments of three genes appearing as highly upregulated in each pathway showed no difference in expression according to the HGP.

conclusionThe current study demonstrates the poor prognostic value carried by IGP in OC and suggests angiogenesis, EMT and inflammation as key carcinogenetic pathways upregulated in this pattern.

Indexed as

AdenocarcinomaAgedBelgiumCarcinoma, Squamous CellCell ProliferationCohort StudiesData ManagementEpithelial-Mesenchymal TransitionEsophageal NeoplasmsFemaleGene Expression Regulation, NeoplasticHumansInflammationMaleMiddle AgedNeoplasm Invasivenesshistopathologymolecular biologyoesophageal cancer

Identifiers

PMID32675198
PMCPMC7368551

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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.