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Adherence to the World Cancer Research Fund/American Institute for Cancer Research cancer prevention recommendations and WNT-pathway-related markers of bowel cancer risk

Published online by Cambridge University Press:  26 September 2018

Fiona C. Malcomson
Affiliation:
Human Nutrition Research Centre, Institute of Cellular Medicine, Newcastle University, Framlington Place, Newcastle upon TyneNE2 4HH, UK
Naomi D. Willis
Affiliation:
Human Nutrition Research Centre, Institute of Cellular Medicine, Newcastle University, Framlington Place, Newcastle upon TyneNE2 4HH, UK
Iain McCallum
Affiliation:
Human Nutrition Research Centre, Institute of Cellular Medicine, Newcastle University, Framlington Place, Newcastle upon TyneNE2 4HH, UK
Long Xie
Affiliation:
Human Nutrition Research Centre, Institute of Cellular Medicine, Newcastle University, Framlington Place, Newcastle upon TyneNE2 4HH, UK
Seamus Kelly
Affiliation:
Human Nutrition Research Centre, Institute of Cellular Medicine, Newcastle University, Framlington Place, Newcastle upon TyneNE2 4HH, UK
David Michael Bradburn
Affiliation:
Human Nutrition Research Centre, Institute of Cellular Medicine, Newcastle University, Framlington Place, Newcastle upon TyneNE2 4HH, UK
Nigel J. Belshaw
Affiliation:
Quadram Institute, Norwich Research Park, Norwich, NorfolkNR4 7UA, UK
Ian T. Johnson
Affiliation:
Quadram Institute, Norwich Research Park, Norwich, NorfolkNR4 7UA, UK
John C. Mathers*
Affiliation:
Human Nutrition Research Centre, Institute of Cellular Medicine, Newcastle University, Framlington Place, Newcastle upon TyneNE2 4HH, UK
*
*Corresponding author: Professor J. C. Mathers, fax +44 1912081101, email john.mathers@ncl.ac.uk
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Abstract

Bowel cancer risk is strongly influenced by lifestyle factors including diet and physical activity. Several studies have investigated the effects of adherence to the World Cancer Research Fund (WCRF)/American Institute for Cancer Research (AICR) cancer prevention recommendations on outcomes such as all-cause and cancer-specific mortality, but the relationships with molecular mechanisms that underlie the effects on bowel cancer risk are unknown. This study aimed to investigate the relationships between adherence to the WCRF/AICR cancer prevention recommendations and wingless/integrated (WNT)-pathway-related markers of bowel cancer risk, including the expression of WNT pathway genes and regulatory microRNA (miRNA), secreted frizzled-related protein 1 (SFRP1) methylation and colonic crypt proliferative state in colorectal mucosal biopsies. Dietary and lifestyle data from seventy-five healthy participants recruited as part of the DISC Study were used. A scoring system was devised including seven of the cancer prevention recommendations and smoking status. The effects of total adherence score and scores for individual recommendations on the measured outcomes were assessed using Spearman’s rank correlation analysis and unpaired t tests, respectively. Total adherence score correlated negatively with expression of Myc proto-oncogene (c-MYC) (P=0·039) and WNT11 (P=0·025), and high adherers had significantly reduced expression of cyclin D1 (CCND1) (P=0·042), WNT11 (P=0·012) and c-MYC (P=0·048). Expression of axis inhibition protein 2 (AXIN2), glycogen synthase kinase (GSK3β), catenin β1 (CTNNB1) and WNT11 and of the oncogenic miRNA miR-17 and colonic crypt kinetics correlated significantly with scores for individual recommendations, including body fatness, red meat intake, plant food intake and smoking status. The findings from this study provide evidence for positive effects of adherence to the WCRF/AICR cancer prevention recommendations on WNT-pathway-related markers of bowel cancer risk.

Information

Type
Full Papers
Copyright
© The Authors 2018 
Figure 0

Table 1 Adherence score assignment for each World Cancer Research Fund (WCRF)/American Institute for Cancer Research (AICR) recommendation

Figure 1

Table 2 Characteristics of the DISC Study participants (Mean values and standard deviations; numbers and percentages)

Figure 2

Table 3 Lifestyle characteristics of DISC Study participants (Mean values and standard deviations; numbers and percentages)

Figure 3

Fig. 1 Clustering of adherence to World Cancer Research Fund/American Institute for Cancer Research cancer prevention recommendations specific to bowel cancer. Data refer to the numbers of participants adhering to each specific recommendation.

Figure 4

Fig. 2 Correlation between total score for adherence to the World Cancer Research Fund/American Institute for Cancer Research recommendations and (a) Myc proto-oncogene (c-MYC) expression and (b) wingless/integrated (WNT)11 expression. Expression of c-MYC and WNT11 is presented as adjusted copies ($$2^{{{\minus}\Delta C_{{\rm t}} }} $$×10 000) relative to 18S and β2M genes.

Figure 5

Table 4 Adherence scores by DISC Study participants for each individual World Cancer Research Fund (WCRF)/American Institute for Cancer Research (AICR) recommendation for cancer prevention (Numbers and percentages, mean values and standard deviations)

Figure 6

Fig. 3 Relationships between adherence scores for individual World Cancer Research Fund/American Institute for Cancer Research recommendations and colorectal mucosal biomarkers. Values are means, with their standard errors represented by vertical bars. Gene expression data are adjusted copies ($$2^{{{\minus}\Delta C_{{\rm t}} }} $$×10 000) relative to 18S and β2M housekeeping genes. microRNA expression data are presented as adjusted copies ($$2^{{{\minus}\Delta C_{{\rm t}} }} $$×10 000) relative to RNU-6 and SNORD68. * P<0·05 for differences between scores analysed using unpaired t tests. AXIN2, axis inhibition protein 2; GSK3β; glycogen synthase kinase; WNT11, wingless/integrated 11; miR-17, miRNa-7; CTNNB1, catenin β1.

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