TY - JOUR
T1 - CYP1A1, CYP2E1, GSTM1, GSTT1, EPHX1 exons 3 and 4,
and NAT2 polymorphisms, smoking, consumption of alcohol
and fruit and vegetables and risk of head and neck cancer
AU - Boccia, Stefania
AU - Cadoni, Gabriella
AU - Fakhredin A., Sayed Tabatabaei
AU - Volante, Mariangela
AU - Arzani, Dario
AU - De Lauretis, Paolo
AU - Cattel, Caterina
AU - Almadori, Giovanni
AU - Van Duijn, Cornelia M.
AU - Paludetti, Gateano
AU - Ricciardi, Walter
PY - 2007
Y1 - 2007
N2 - Purpose As risk-modiWers of alcohol and tobacco eVects,
metabolic genes polymorphisms were investigated as susceptibility
candidates for squamous cell carcinoma of the
head and neck (SCCHN).
Methods A total of 210 cases and 245 hospital controls,
age and gender matched, were genotyped for CYP1A1,
CYP2E1, GSTM1, GSTT1, EPHX1 exons 3 and 4, and
NAT2 polymorphisms. A measurement of the biological
interaction among two risk factors was estimated by the
attributable proportion (AP) due to interaction and its 95%
conWdence interval (CI).
Results SCCHN risk was associated with high-levels of
alcohol intake [OR = 3.50 (95%CI: 1.93 6.35) and OR = 6.47
(95%CI: 2.92 14.35) for 19 30 g/day and >30 g/day, respectively],
cigarette smoking [OR = 3.47 (95%CI: 1.88 6.41)
and OR = 7.65 (95%CI: 4.20 13.90) for 1 25 and >25 packyears
of smoking, respectively] and low-fruit and vegetables
consumption (OR = 2.45; 95%CI: 1.53 3.92). No diVerences
were observed for the genotypes or haplotypes distributions
among cases and controls, and no biological interaction
emerged from gene gene and gene environment interaction
analyses. An attributable proportion (AP) due to biological
interaction of 0.65 (95%CI: 0.40 0.90) was detected for
heavy drinkers with a low intake of fruit and vegetables, and
an AP of 0.40 (95%CI: 0.10 0.72) resulted forever smokers
with low fruit and vegetables consumption.
Conclusions Even in presence of high alcohol consumption
or cigarette smoking, a high intake of fruit and vegetables
might prevent the development of around one quarter
of SCCHN cases. The lack of interaction between the studied
polymorphisms and the environmental exposures suggests
that chronic consumption of tobacco and alcohol
overwhelm enzyme defences, irrespective of genotype.
AB - Purpose As risk-modiWers of alcohol and tobacco eVects,
metabolic genes polymorphisms were investigated as susceptibility
candidates for squamous cell carcinoma of the
head and neck (SCCHN).
Methods A total of 210 cases and 245 hospital controls,
age and gender matched, were genotyped for CYP1A1,
CYP2E1, GSTM1, GSTT1, EPHX1 exons 3 and 4, and
NAT2 polymorphisms. A measurement of the biological
interaction among two risk factors was estimated by the
attributable proportion (AP) due to interaction and its 95%
conWdence interval (CI).
Results SCCHN risk was associated with high-levels of
alcohol intake [OR = 3.50 (95%CI: 1.93 6.35) and OR = 6.47
(95%CI: 2.92 14.35) for 19 30 g/day and >30 g/day, respectively],
cigarette smoking [OR = 3.47 (95%CI: 1.88 6.41)
and OR = 7.65 (95%CI: 4.20 13.90) for 1 25 and >25 packyears
of smoking, respectively] and low-fruit and vegetables
consumption (OR = 2.45; 95%CI: 1.53 3.92). No diVerences
were observed for the genotypes or haplotypes distributions
among cases and controls, and no biological interaction
emerged from gene gene and gene environment interaction
analyses. An attributable proportion (AP) due to biological
interaction of 0.65 (95%CI: 0.40 0.90) was detected for
heavy drinkers with a low intake of fruit and vegetables, and
an AP of 0.40 (95%CI: 0.10 0.72) resulted forever smokers
with low fruit and vegetables consumption.
Conclusions Even in presence of high alcohol consumption
or cigarette smoking, a high intake of fruit and vegetables
might prevent the development of around one quarter
of SCCHN cases. The lack of interaction between the studied
polymorphisms and the environmental exposures suggests
that chronic consumption of tobacco and alcohol
overwhelm enzyme defences, irrespective of genotype.
KW - HNC
KW - POLYMORPHISMS
KW - HNC
KW - POLYMORPHISMS
UR - http://hdl.handle.net/10807/193490
M3 - Article
SN - 0171-5216
VL - 2008
SP - 93
EP - 108
JO - Journal of Cancer Research and Clinical Oncology
JF - Journal of Cancer Research and Clinical Oncology
ER -