Evidence map›Paper›PMID 32268844›Full record

ReviewUnited European gastroenterology journal2020

Genomic and molecular alterations in human inflammatory bowel disease-associated colorectal cancer.

Marie Muller, Franck Hansmannel, Djesia Arnone, Myriam Choukour, Ndeye Coumba Ndiaye, Tunay Kokten, Rémi Houlgatte, Laurent Peyrin-Biroulet

Open access · bronzeAbstract readReview
In one paragraph

Review in United European gastroenterology journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
8.1field-weighted citation impact, top 2% 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

21 citing papers in PubMed, 55 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Epigenetics of Inflammatory Bowel Diseases.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2023
    Article
  14. Annals of medicine · 2023
    Article
  15. Article
  16. Tumor Suppressor microRNAs in Gastrointestinal Cancers: A Mini-Review.Recent advances in inflammation & allergy drug discovery · 2022
    Review
  17. Article
  18. Article
  19. Article
  20. 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

8 authors at 2 institutions in 1 country.

Marie MullerDepartment of Gastroenterology, Nancy University Hospital, University of Lorraine, France.ORCID 0000-0001-6412-932X
Franck HansmannelInserm U1256 "Nutrition - Genetics and exposure to environmental risks - NGERE", Nancy, France.ORCID 0000-0003-1661-2362
Djesia ArnoneInserm U1256 "Nutrition - Genetics and exposure to environmental risks - NGERE", Nancy, France.
Myriam ChoukourDepartment of Gastroenterology, Nancy University Hospital, University of Lorraine, France.
Ndeye Coumba NdiayeInserm U1256 "Nutrition - Genetics and exposure to environmental risks - NGERE", Nancy, France.
Tunay KoktenInserm U1256 "Nutrition - Genetics and exposure to environmental risks - NGERE", Nancy, France.
Rémi HoulgatteInserm U1256 "Nutrition - Genetics and exposure to environmental risks - NGERE", Nancy, France.
Laurent Peyrin-BirouletDepartment of Gastroenterology, Nancy University Hospital, University of Lorraine, France.
Inserm · FRUniversité de Lorraine · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Patients with inflammatory bowel disease are at increased risk of colorectal cancer, which has worse prognosis than sporadic colorectal cancer. Until recently, understanding of pathogenesis in inflammatory bowel disease-associated colorectal cancer was restricted to the demonstration of chromosomic/microsatellite instabilities and aneuploidy. The advance of high-throughput sequencing technologies has highlighted the complexity of the pathobiology and revealed recurrently mutated genes involved in the RTK/RAS, PI3K, WNT, and TGFβ pathways, leading to potentially new targetable mutations. Moreover, alterations of mitochondrial DNA and the dysregulation of non-coding sequences have also been described, as well as several epigenetic modifications. Although recent studies have brought new insights into pathobiology and raised the prospect of innovative therapeutic approaches, the understanding of colorectal carcinogenesis in inflammatory bowel disease and how it differs from sporadic colorectal cancer remains not fully elucidated. Further studies are required to better understand the pathogenesis and molecular alterations leading to human inflammatory bowel disease-associated colorectal cancer.

Indexed as

Biomarkers, TumorCarcinogenesisColitis-Associated NeoplasmsColitis, UlcerativeCrohn DiseaseDNA, MitochondrialDNA Mutational AnalysisEpigenesis, GeneticGastrointestinal MicrobiomeHigh-Throughput Nucleotide SequencingHost Microbial InteractionsHumansIntestinal MucosaMutationRNA, UntranslatedSignal TransductionBiomarkers, TumorDNA, MitochondrialRNA, Untranslatedcolorectal cancerepigeneticsgenomicsInflammatory bowel diseaseinflammatory bowel disease-associated cancermolecular pathways

Identifiers

PMID32268844
PMCPMC7437079
OpenAlexW3015870096

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.