Sirtuin 1 genetic variation, energy balance and colorectal cancer risk by sex and subsite in the Netherlands Cohort Study

Sirtuin 1 (SIRT1) is an energy-sensing protein, which may affect tumorigenesis. We used SIRT1 variants as time-independent indicators of SIRT1 involvement in carcinogenesis and we studied two tagging SIRT1 variants in relation to colorectal cancer (CRC) risk. We also evaluated known energy balance-related CRC risk factors within SIRT1 genotype strata. The Netherlands Cohort Study includes 120,852 individuals and has 20.3 years follow-up (case-cohort: n(subcohort) = 5000; n(CRC cases) = 4667). At baseline, participants self-reported weight, weight at age 20, height, trouser/skirt size reflectin... Mehr ...

Verfasser: Simons, C. C. J. M.
Schouten, L. J.
Godschalk, R. W.
van Schooten, F. J.
van den Brandt, P. A.
Weijenberg, M. P.
Dokumenttyp: Artikel
Erscheinungsdatum: 2018
Reihe/Periodikum: Simons , C C J M , Schouten , L J , Godschalk , R W , van Schooten , F J , van den Brandt , P A & Weijenberg , M P 2018 , ' Sirtuin 1 genetic variation, energy balance and colorectal cancer risk by sex and subsite in the Netherlands Cohort Study ' , Scientific Reports , vol. 8 , 16540 . https://doi.org/10.1038/s41598-018-34728-6
Schlagwörter: SCALE PROSPECTIVE COHORT / BLOOD MONONUCLEAR-CELLS / GROWTH-FACTOR PATHWAY / PHYSICAL-ACTIVITY / BODY-SIZE / ANTHROPOMETRIC VARIABLES / FOLLOW-UP / ASSOCIATION / CARCINOMA / WOMEN
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-27206253
Datenquelle: BASE; Originalkatalog
Powered By: BASE
Link(s) : https://cris.maastrichtuniversity.nl/en/publications/6f883c54-fee7-4b26-a26d-7216bd18b023

Sirtuin 1 (SIRT1) is an energy-sensing protein, which may affect tumorigenesis. We used SIRT1 variants as time-independent indicators of SIRT1 involvement in carcinogenesis and we studied two tagging SIRT1 variants in relation to colorectal cancer (CRC) risk. We also evaluated known energy balance-related CRC risk factors within SIRT1 genotype strata. The Netherlands Cohort Study includes 120,852 individuals and has 20.3 years follow-up (case-cohort: n(subcohort) = 5000; n(CRC cases) = 4667). At baseline, participants self-reported weight, weight at age 20, height, trouser/skirt size reflecting waist circumference, physical activity, and early life energy restriction. SIRT1 rs12778366 and rs10997870 were genotyped in toenail DNA available for similar to 75% of the cohort. Sex-and subsite-specific Cox hazard ratios (HRs) showed that the rs12778366 CC versus TT genotype decreased CRC and colon cancer risks in women (HRCRC = 0.53, 95% confidence interval: 0.30-0.94) but not men. Multiplicative interactions were observed between SIRT1 variants and energy balance-related factors in relation to CRC endpoints, but the direction of associations was not always conform expectation nor specific to one genotype stratum. In conclusion, these results support SIRT1 involvement in colon cancer development in women. No conclusions could be made regarding a modifying effect of SIRT1 variants on associations between energy balance-related factors and CRC risk.