Background: Representing the second cause of cancer-related death after lung cancer in men and breast cancer in women, colorectal cancer (CRC) is a major health problemin Italy. Obesity is reckoned to favor CRC; however, the underlying mechanisms are unclear. Recently, a single nucleotide polymorphism (SNP) in the fat mass and obesity associated (FTO) gene was found to be significantly associated with obesity. Aims: To establish whether the FTO SNP rs9939609 may represent a risk factor for CRC and adenoma in the Italian population. Patients and methods: 1,037 subjects were enrolled in the study and divided in 3 groups: CRC (341 pts., M/F=197/144, mean age=65.17 +/- 11.16 years), colorectal adenoma (385 pts., M/F=247/138, mean age=62.49 +/- 13.01 years), healthy controls (311 pts., M/F=150/161, mean age=57.31 +/- 13.84 years). DNA was extracted from whole blood, and stored frozen for rs9939609 genotyping by real-time PCR. Results: The frequency of the obesity-associatedmutated A allele (AA+AT) on the FTO gene was 69.77% among controls, and 71.85% and 65.71% respectively among CRC and polyp patients. Compared to control subjects the AA+AT genotype had no significant effect on the risk for either CRC (OR=1.106; CI 95%=0.788-1.550; p=0.561) or colorectal adenomas (OR=0.830; CI 95%=0.602-1.144; p=0.255). We did not observe any association between the AA genotype and CRC/polyp localization and age at diagnosis. As measured in a patient subset, carriership of the risk alleles did not reflect in a significantly altered BMI. Conclusion: The obesity-linked FTO variants do not play a significant role in modulating the colorectal cancer risk in the Italian population. (C) 2011 European Federation of Internal Medicine. Published by Elsevier B.V. All rights reserved

The obesity gene and colorectal cancer risk: a population study in Northern Italy.

CODA, Renato;
2012-01-01

Abstract

Background: Representing the second cause of cancer-related death after lung cancer in men and breast cancer in women, colorectal cancer (CRC) is a major health problemin Italy. Obesity is reckoned to favor CRC; however, the underlying mechanisms are unclear. Recently, a single nucleotide polymorphism (SNP) in the fat mass and obesity associated (FTO) gene was found to be significantly associated with obesity. Aims: To establish whether the FTO SNP rs9939609 may represent a risk factor for CRC and adenoma in the Italian population. Patients and methods: 1,037 subjects were enrolled in the study and divided in 3 groups: CRC (341 pts., M/F=197/144, mean age=65.17 +/- 11.16 years), colorectal adenoma (385 pts., M/F=247/138, mean age=62.49 +/- 13.01 years), healthy controls (311 pts., M/F=150/161, mean age=57.31 +/- 13.84 years). DNA was extracted from whole blood, and stored frozen for rs9939609 genotyping by real-time PCR. Results: The frequency of the obesity-associatedmutated A allele (AA+AT) on the FTO gene was 69.77% among controls, and 71.85% and 65.71% respectively among CRC and polyp patients. Compared to control subjects the AA+AT genotype had no significant effect on the risk for either CRC (OR=1.106; CI 95%=0.788-1.550; p=0.561) or colorectal adenomas (OR=0.830; CI 95%=0.602-1.144; p=0.255). We did not observe any association between the AA genotype and CRC/polyp localization and age at diagnosis. As measured in a patient subset, carriership of the risk alleles did not reflect in a significantly altered BMI. Conclusion: The obesity-linked FTO variants do not play a significant role in modulating the colorectal cancer risk in the Italian population. (C) 2011 European Federation of Internal Medicine. Published by Elsevier B.V. All rights reserved
2012
23
65
69
http://dx.doi.org/10.1016/j.ejim.2011.07.011
Colorectal cancer, FTO gene, Genotype, Single nucleotide polymorphism, Obesity
E. Tarabra;G. C. Actis;M. Fadda;P. D. Paolis;A. Comandone;R. Coda;F. Rosina
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/99912
Citazioni
  • ???jsp.display-item.citation.pmc??? 9
  • Scopus 19
  • ???jsp.display-item.citation.isi??? 21
social impact