Evidence map›Paper›PMID 36067202›Full record

ArticlePloS one2022

Colorectal cancer-associated SNP rs17042479 is involved in the regulation of NAF1 promoter activity.

Josephine B Olsson, Marietta B Gugerel, Stine B Jessen, Jannie Jørgensen, Ismail Gögenur, Camilla Hansen, Lene T Kirkeby, Jørgen Olsen, Ole B V Pedersen, Peter M Vestlev and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2022. 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
0.2field-weighted citation impact, top 52% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  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

12 authors at 5 institutions in 1 country.

Josephine B OlssonDepartment of Science and Environment, Roskilde University, Roskilde, Denmark.
Marietta B GugerelDepartment of Science and Environment, Roskilde University, Roskilde, Denmark.
Stine B JessenDepartment of Science and Environment, Roskilde University, Roskilde, Denmark.
Jannie JørgensenDepartment of Science and Environment, Roskilde University, Roskilde, Denmark.
Ismail GögenurCenter for Surgical Science, Enhanced Perioperative Oncology (EPeOnc) Consortium, Department of Surgery, Zealand University Hospital, Køge, Denmark.
Camilla HansenDepartment of Science and Environment, Roskilde University, Roskilde, Denmark.
Lene T KirkebyCenter for Surgical Science, Enhanced Perioperative Oncology (EPeOnc) Consortium, Department of Surgery, Zealand University Hospital, Køge, Denmark.
Jørgen OlsenFaculty of Health and Medical Sciences, Copenhagen University, Copenhagen, Denmark.
Ole B V PedersenDepartment of Clinical Immunology, Zealand University Hospital, Naestved, Denmark.
Peter M VestlevDepartment of Oncology, Roskilde Hospital, Roskilde, Denmark.
Katja DahlgaardDepartment of Science and Environment, Roskilde University, Roskilde, Denmark.ORCID 0000-0002-2822-4685
Jesper T TroelsenDepartment of Science and Environment, Roskilde University, Roskilde, Denmark.ORCID 0000-0002-4177-3267
Roskilde University · DKZealand University Hospital Køge · DKRoskilde Sygehus · DKUniversity of Copenhagen · DKZealand University Hospital · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A novel risk locus at 4q32.2, located between the Nuclear Assembly Factor 1 (NAF1) and Follistatin Like 5 (FSTL5) genes, was associated with increased risk of developing colorectal cancer (CRC), with SNP rs17042479 being the most associated. However, the link between CRC development and the risk locus at 4q32.2 is unknown. We investigated the promoter activity of NAF1 and FSTL5 and analyzed the risk locus at 4q32.2 as gene regulatory region. Our results showed that the activity of the FSTL5 promoter was low compared to the NAF1 promoter. Analyses of the NAF1 promoter in conjunction with the region containing the risk locus at 4q32.2 showed that the region functions as gene regulatory region with repressor activity on NAF1 promoter activity. The SNP rs17042479(G) increased the repressor effect of the region. CRC patients' biopsies were genotyped for SNP rs17042479(A/G), and NAF1 expression profiles were examined. We found an association between SNP rs17042479(G), cancer stage and tumor location. Additionally, patients with SNP rs17042479(G) showed lower NAF1 expression in comparison to patients with SNP rs17042479(A) in tumor tissue and the NAF1 expression in tumor tissue was lower compared to healthy tissue. The results in the study imply that reduced NAF1 expression in the tumor contribute to a more aggressive phenotype. Furthermore, this study suggests that the SNP rs17042479(G) change the expression of NAF1 and thereby increases the risk of developing CRC.

Indexed as

Colorectal NeoplasmsNFI Transcription FactorsGenotypeHumansPolymorphism, Single NucleotidePromoter Regions, GeneticRibonucleoproteinsNAF1 protein, humanNFI Transcription FactorsRibonucleoproteins

Identifiers

PMID36067202
PMCPMC9447907
OpenAlexW4294843849

What OpenQuestion holds

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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.