Evidence map›Paper›PMID 35807897›Full record

ArticleNutrients2022

The Associations of Selenoprotein Genetic Variants with the Risks of Colorectal Adenoma and Colorectal Cancer: Case-Control Studies in Irish and Czech Populations.

Maryam Mukhtar, Niall Ashfield, Ludmila Vodickova, Veronika Vymetalkova, Miroslav Levy, Václav Liska, Jan Bruha, Petra Bendova, Jacintha O'Sullivan, Glen Doherty and 4 more

Open access · goldAbstract read
In one paragraph

Article in Nutrients, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. "Alphabet" Selenoproteins: Their Characteristics and Physiological Roles.International journal of molecular sciences · 2023
    Review
  5. Review
  6. Article
  7. Review
  8. Selenoprotein S: A versatile disordered protein.Archives of biochemistry and biophysics · 2022
    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

14 authors at 5 institutions in 2 countries.

Maryam MukhtarCancer Biology and Therapeutics Group, School of Biomolecular and Biomedical Science, UCD Conway Institute, University College Dublin, D04 V1W8 Dublin, Ireland.ORCID 0000-0003-3571-5447
Niall AshfieldCancer Biology and Therapeutics Group, School of Biomolecular and Biomedical Science, UCD Conway Institute, University College Dublin, D04 V1W8 Dublin, Ireland.ORCID 0000-0002-1536-5366
Ludmila VodickovaInstitute of Biology and Medical Genetics, First Faculty of Medicine, Charles University, 121 08 Prague, Czech Republic.
Veronika VymetalkovaInstitute of Biology and Medical Genetics, First Faculty of Medicine, Charles University, 121 08 Prague, Czech Republic.
Miroslav LevyDepartment of Surgery, First Faculty of Medicine, Charles University and Thomayer Hospital, 121 08 Prague, Czech Republic.
Václav LiskaBiomedical Centre, Faculty of Medicine in Pilsen, Charles University, 323 00 Pilsen, Czech Republic.
Jan BruhaBiomedical Centre, Faculty of Medicine in Pilsen, Charles University, 323 00 Pilsen, Czech Republic.
Petra BendovaInstitute of Experimental Medicine ASCR, 142 20 Prague, Czech Republic.
Jacintha O'SullivanTrinity Translational Medicine Institute, Department of Surgery, Trinity College Dublin and St. James's Hospital, D08 NHY1 Dublin, Ireland.
Glen DohertyCentre for Colorectal Disease, St. Vincent's University Hospital, D04 T6F4 Dublin, Ireland.
Kieran SheahanCentre for Colorectal Disease, St. Vincent's University Hospital, D04 T6F4 Dublin, Ireland.
Blathnaid NolanCentre for Colorectal Disease, St. Vincent's University Hospital, D04 T6F4 Dublin, Ireland.
Pavel VodickaInstitute of Biology and Medical Genetics, First Faculty of Medicine, Charles University, 121 08 Prague, Czech Republic.
David J HughesCancer Biology and Therapeutics Group, School of Biomolecular and Biomedical Science, UCD Conway Institute, University College Dublin, D04 V1W8 Dublin, Ireland.ORCID 0000-0003-1668-8770
Charles University · CZSt. Vincent's University Hospital · IEUniversity College Dublin · IECzech Academy of Sciences, Institute of Experimental Medicine · CZTrinity College Dublin · IE

Funding

Czech Health Research council of the Ministry of Health of the Czech Republic AZV NV18-03-00199Czech Science Foundation GACR 20-03997SCzech Science Foundation VV 22-05942SHealth Research Board of Ireland HRA-POS/2013/397International Hundred K+ Cohorts Consortium/Global Genomic Medicine Collaborative (IHCC/G2MC) 31312020
6 · The paper itself

Abstract

backgroundSelenium manifests its biological effects through its incorporation into selenoproteins, which play several roles in countering oxidative and inflammatory responses implicated in colorectal carcinogenesis. Selenoprotein genetic variants may contribute to colorectal cancer (CRC) development, as we previously observed for SNP variants in a large European prospective study and a Czech case-control cohort.

methodsWe tested if significantly associated selenoprotein gene SNPs from these studies were also associated with CRC risk in case-control studies from Ireland (colorectal neoplasia, i.e., cancer and adenoma cases: 450, controls: 461) and the Czech Republic (CRC cases: 718, controls: 646). Genotyping of 23 SNPs (20 in the Irish and 13 in the Czechs) was performed by competitive specific allele-specific PCR (KASPar). Multivariable adjusted logistic regression was used to assess the associations with CRC development.

resultsWe found significant associations with an increased CRC risk for rs5859 (

conclusionsSeveral SNPs previously associated with CRC risk were also associated with CRC or colorectal neoplasia development in either the Irish or Czech cohorts. Selenoprotein gene variation may modify CRC risk across diverse European populations, although the specific variants may differ.

Indexed as

AdenomaColorectal NeoplasmsCase-Control StudiesCzech RepublicGenetic Predisposition to DiseaseHumansPolymorphism, Single NucleotideProspective StudiesSelenoprotein PSelenoproteinsSelenoprotein PSelenoproteinscase–control cohortscolorectal cancer riskcolorectal neoplasmsSeleniumSelenium pathwayselenoprotein gene variation

Identifiers

PMID35807897
PMCPMC9268344
OpenAlexW4283720065

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.