SwePub
Sök i LIBRIS databas

  Extended search

WFRF:(Bas Anna)
 

Search: WFRF:(Bas Anna) > Association of Sele...

Association of Selenoprotein and Selenium Pathway Genotypes with Risk of Colorectal Cancer and Interaction with Selenium Status

Fedirko, Veronika (author)
Jenab, Mazda (author)
Meplan, Catherine (author)
show more...
Jones, Jeb S. (author)
Zhu, Wanzhe (author)
Schomburg, Lutz (author)
Siddiq, Afshan (author)
Hybsier, Sandra (author)
Overvad, Kim (author)
Tjonneland, Anne (author)
Omichessan, Hanane (author)
Perduca, Vittorio (author)
Boutron-Ruault, Marie-Christine (author)
Kuehn, Tilman (author)
Katzke, Verena (author)
Aleksandrova, Krasimira (author)
Trichopoulou, Antonia (author)
Karakatsani, Anna (author)
Kotanidou, Anastasia (author)
Tumino, Rosario (author)
Panico, Salvatore (author)
Masala, Giovanna (author)
Agnoli, Claudia (author)
Naccarati, Alessio (author)
Bueno-de-Mesquita, Bas (author)
Vermeulen, Roel C. H. (author)
Weiderpass, Elisabete (author)
Karolinska Institutet
Skeie, Guri (author)
Nost, Therese Haugdahl (author)
Lujan-Barroso, Leila (author)
Ramon Quiros, J. (author)
Maria Huerta, Jose (author)
Rodriguez-Barranco, Miguel (author)
Barricarte, Aurelio (author)
Gylling, Björn, 1978- (author)
Umeå universitet,Patologi
Harlid, Sophia, 1978- (author)
Umeå universitet,Onkologi
Bradbury, Kathryn E. (author)
Wareham, Nick (author)
Khaw, Kay-Tee (author)
Gunter, Marc (author)
Murphy, Neil (author)
Freisling, Heinz (author)
Tsilidis, Kostas (author)
Aune, Dagfinn (author)
Riboli, Elio (author)
Hesketh, John E. (author)
Hughes, David J. (author)
show less...
 (creator_code:org_t)
2019-04-25
2019
English.
In: Nutrients. - : MDPI. - 2072-6643. ; 11:4
  • Journal article (peer-reviewed)
Abstract Subject headings
Close  
  • Selenoprotein genetic variations and suboptimal selenium (Se) levels may contribute to the risk of colorectal cancer (CRC) development. We examined the association between CRC risk and genotype for single nucleotide polymorphisms (SNPs) in selenoprotein and Se metabolic pathway genes. Illumina Goldengateassays were designed and resulted in the genotyping of 1040 variants in 154 genes from 1420 cases and 1421 controls within the European Prospective Investigation into Cancer and Nutrition (EPIC) study. Multivariable logistic regression revealed an association of 144 individual SNPs from 63 Se pathway genes with CRC risk. However, regarding the selenoprotein genes, only TXNRD1 rs11111979 retained borderline statistical significance after adjustment for correlated tests (PACT = 0.10; PACT significance threshold was P < 0.1). SNPs in Wingless/Integrated (Wnt) and Transforming growth factor (TGF) beta-signaling genes (FRZB, SMAD3, SMAD7) from pathways affected by Se intake were also associated with CRC risk after multiple testing adjustments. Interactions with Se status (using existing serum Se and Selenoprotein P data) were tested at the SNP, gene, and pathway levels. Pathway analyses using the modified Adaptive Rank Truncated Product method suggested that genes and gene x Se status interactions in antioxidant, apoptosis, and TGF-beta signaling pathways may be associated with CRC risk. This study suggests that SNPs in the Se pathway alone or in combination with suboptimal Se status may contribute to CRC development.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Hälsovetenskap -- Näringslära (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Health Sciences -- Nutrition and Dietetics (hsv//eng)

Keyword

selenium
selenium status
selenoprotein gene variation
selenium pathway
colorectal neoplasms
selenoprotein P
prospective cohort
colorectal cancer risk
genetic epidemiology
biomarkers

Publication and Content Type

ref (subject category)
art (subject category)

Find in a library

  • Nutrients (Search for host publication in LIBRIS)

To the university's database

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Close

Copy and save the link in order to return to this view