Evidence map›Paper›PMID 35432477›Full record

ArticleFrontiers in genetics2022

Identification of Common and Distinct Pathways in Inflammatory Bowel Disease and Colorectal Cancer: A Hypothesis Based on Weighted Gene Co-Expression Network Analysis.

Afshin Derakhshani, Darya Javadrashid, Nima Hemmat, Antoine Dufour, Antonio Giovanni Solimando, Mahdi Abdoli Shadbad, Pascal H G Duijf, Oronzo Brunetti, Nicola Silvestris, Behzad Baradaran

Open access · goldAbstract read
In one paragraph

Article in Frontiers in genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

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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 6 institutions in 5 countries.

Afshin DerakhshaniDepartment of Biochemistry and Molecular Biology, University of Calgary, Calgary, AB, Canada.
Darya JavadrashidImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Nima HemmatImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Antoine DufourDepartments of Physiology and Pharmacology, University of Calgary, Calgary, AB, Canada.
Antonio Giovanni SolimandoDepartment of Biomedical Sciences and Human Oncology, School of Medicine, Aldo Moro University of Bari, Bari, Italy.
Mahdi Abdoli ShadbadStudent Research Committee, Tabriz University of Medical Sciences, Tabriz, Iran.
Pascal H G DuijfSchool of Biomedical Sciences, Faculty of Health, Queensland University of Technology, Brisbane, QLD, Australia.
Oronzo BrunettiMedical Oncology Unit, IRCCS Istituto Tumori Giovanni Paolo II, Bari, Italy.
Nicola SilvestrisMedical Oncology Unit, Department of Human Pathology "G. Barresi" , University of Messina, Messina, Italy.
Behzad BaradaranImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Tabriz University of Medical Sciences · IRUniversity of Calgary · CAIstituti di Ricovero e Cura a Carattere Scientifico · ITTranslational Research Institute · AUUniversity of Bari Aldo Moro · ITUniversity of Messina · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Patients with inflammatory bowel disease (IBD), including ulcerative colitis and Crohn's disease, are at higher risk to develop colorectal cancer (CRC). However, the underlying mechanisms of this predisposition remain elusive. We performed in-depth comparative computational analyses to gain new insights, including weighted gene co-expression network analysis (WGCNA) and gene ontology and pathway enrichment analyses, using gene expression datasets from IBD and CRC patients. When individually comparing IBD and CRC to normal control samples, we identified clusters of highly correlated genes, differentially expressed genes, and module-trait associations specific for each disease. When comparing IBD to CRC, we identified common hub genes and commonly enriched pathways. Most notably, IBD and CRC share significantly increased expression of five genes (

Indexed as

colorectal cancerinflammatory bowel diseasepathogenesissystems biologyWGCNA

Identifiers

PMID35432477
PMCPMC9008839
OpenAlexW4221088064

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.