Pleural malignant mesothelioma, genetic susceptibility and asbestos exposure

被引:29
|
作者
Neri, M
Filiberti, R
Taioli, E
Garte, S
Paracchini, V
Bolognesi, C
Canessa, PA
Fontana, V
Ivaldi, GP
Verna, A
Bonassi, S
Puntoni, R
机构
[1] Ist Nazl Ric Canc, Unit Epidemiol & Biostat, I-16132 Genoa, Italy
[2] Ist Nazl Ric Canc, Unit Environm Carcinogenesis, I-16132 Genoa, Italy
[3] Ist Nazl Ric Canc, Unit Surg Oncol B, I-16132 Genoa, Italy
[4] Ist Nazl Ric Canc, Unit Mol Epidemiol, I-16132 Genoa, Italy
[5] IRCCS, Fondaz Policlin, Milan, Italy
[6] Osped S Bartolomeo, Unit Pneumol, Sarzana, Italy
关键词
asbestos; mEH; GSTM1; GSTT1; NAT2; CYP1A1; malignant mesothelioma; gene-environment interaction;
D O I
10.1016/j.mrfmmm.2005.06.003
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Pleural malignant mesothelioma (NW) is a rare but extremely aggressive cancer. The limited impact of standard therapeutic treatments on survival rates makes the identification of factors that increase the individual risk a leading priority. The high proportion of cases explained by exposure to asbestos has guided intervention policies to an effective ban of this compound from our environment. However, MM cannot be solely attributed to this agent, and the role of predisposing factors and their interaction with asbestos exposure is increasingly studied. The role of mEH, GSTM1, GSTT1, NAT2, and CYP1A1 genotypes in modulating susceptibility to MM was examined in a case-control study of 80 subjects with a confirmed diagnosis of MM and 255 controls. Subjects with low mEH activity showed a significantly increased risk of MM (OR, 2.51; 95% CI, 1.11-5.68). The association was stronger in the group with low asbestos exposure (OR, 7.83; 95% Cl, 0.98-62.60). A significant increased risk of MM was also found in NAT2 fast acetylators (OR, 1.74; 95% Cl, 1.02-2.96). The presence of synergisms between genotypes, i.e., mEH and NAT2 (LRT for heterogeneity p < 0.023), mEH and GSTM1 (LRT p < 0.061), and NAT2 and GSTM1 (LRT p < 0.049), combined with the interaction observed with exposure to asbestos, suggests the presence of gene-environment and gene-gene interactions in the development of MM, although the size of the study group does not allow to draw clearcut conclusions. Since genetic polymorphisms can also modify the extent of genetic damage occurring in subjects exposed to carcinogens, we measured the frequency of micronuclei in peripheral blood lymphocytes of a subgroup of MM cases. The limited number of cases (28) did not allow to observe significant effects. In conclusion, these results strengthen the hypothesis that individual susceptibility to MM can be modulated by the interaction between polymorphic genes involved in the metabolism and the intensity of asbestos exposure. (c) 2005 Elsevier B.V. All rights reserved.
引用
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页码:36 / 44
页数:9
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