Evidence map›Paper›PMID 34467497›Full record

ArticleAnnals of surgical oncology2021

Colonic Stent as Bridge to Surgery for Malignant Obstruction Induces Gene Expressional Changes Associated with a More Aggressive Tumor Phenotype.

Malene Broholm, Thea Helene Degett, Sara Furbo, Anne-Marie Kanstrup Fiehn, Mustafa Bulut, Thomas Litman, Jens Ole Eriksen, Jesper T Troelsen, Lise Mette Rahbek Gjerdrum, Ismail Gögenur

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Article in Annals of surgical oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 36% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
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 3 institutions in 1 country.

Malene BroholmCenter for Surgical Science, Department of Surgery, Zealand University Hospital, Køge, Denmark. malenebroholm87@gmail.com.ORCID http://orcid.org/0000-0002-0996-8048
Thea Helene DegettCenter for Surgical Science, Department of Surgery, Zealand University Hospital, Køge, Denmark.
Sara FurboCenter for Surgical Science, Department of Surgery, Zealand University Hospital, Køge, Denmark.
Anne-Marie Kanstrup FiehnCenter for Surgical Science, Department of Surgery, Zealand University Hospital, Køge, Denmark.
Mustafa BulutCenter for Surgical Science, Department of Surgery, Zealand University Hospital, Køge, Denmark.
Thomas LitmanDepartment of International Health, Immunology and Microbiology, University of Copenhagen, Copenhagen, Denmark.
Jens Ole EriksenDepartment of Pathology, Zealand University Hospital, Køge, Denmark.
Jesper T TroelsenDepartment of Science and Environment, Roskilde University, Roskilde, Denmark.
Lise Mette Rahbek GjerdrumDepartment of Pathology, Zealand University Hospital, Køge, Denmark.
Ismail GögenurCenter for Surgical Science, Department of Surgery, Zealand University Hospital, Køge, Denmark.
University of Copenhagen · DKZealand University Hospital Køge · DKRoskilde University · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundColonic stent is recommended as a bridge to elective surgery for malignant obstruction to improve short-term clinical outcomes for patients with colorectal cancer. However, since the oncological outcomes remain controversial, this study aimed to investigate the impact of self-expandable metallic stent (SEMS) on the tumor microenvironment.

methodsPatients treated with colonic stent as a bridge to surgery from 2010 to 2015 were identified from hospital records. Tumor biopsies and resected tumor samples of the eligible patients were retrieved retrospectively. Gene expression analysis was performed using the NanoString nCounter PanCancer IO 360 gene expression panel.

resultsOf the 164 patients identified, this study included 21 who underwent colonic stent placement as a bridge to elective surgery. Gene expression analysis revealed 82 differentially expressed genes between pre- and post-intervention specimens, of which 72 were upregulated and 10 downregulated. Among the significantly upregulated genes, 46 are known to have protumor functions, of which 26 are specifically known to induce tumorigenic mechanisms such as proliferation, migration, invasion, angiogenesis, and inflammation. In addition, ten differentially expressed genes were identified that are known to promote antitumor functions.

conclusionSEMS induces gene expressional changes in the tumor microenvironment that are associated with tumor progression in colorectal cancer and may potentiate a more aggressive phenotype. Future studies are warranted to establish optimal timing of surgery after SEMS insertion in patients with obstructive colorectal cancer.

Indexed as

Colorectal NeoplasmsIntestinal ObstructionSelf Expandable Metallic StentsGene ExpressionHumansPhenotypeRetrospective StudiesStentsTreatment OutcomeTumor Microenvironment

Identifiers

PMID34467497
OpenAlexW3197767222

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.