The TP53 gene, tobacco exposure, and lung cancer

被引:211
作者
Toyooka, S
Tsuda, T
Gazdar, AF
机构
[1] Univ Texas, SW Med Ctr, Hamon Ctr Therapeut Oncol Res, Dallas, TX 75390 USA
[2] Univ Texas, SW Med Ctr, Dept Pathol, Dallas, TX 75390 USA
[3] Okayama Univ, Grad Sch Med & Dent, Dept Canc & Thorac Surg, Okayama, Japan
[4] Okayama Univ, Grad Sch Med & Dent, Dept Hyg & Prevent Med, Okayama, Japan
关键词
p53; TP53; cancer; lung cancer; tobacco; exposure; carcinogen; risk factor; mutgen; WILD-TYPE P53; ATYPICAL ALVEOLAR HYPERPLASIA; K-RAS MUTATIONS; MUTAGENIC SIGNATURE; CIGARETTE-SMOKING; PROGNOSTIC-SIGNIFICANCE; RECOMBINANT ADENOVIRUS; BRONCHIAL EPITHELIUM; C-ERBB-2; EXPRESSION; ALPHA-PARTICLES;
D O I
10.1002/humu.10177
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Of the various genetic alterations in lung cancer, the abnormalities of the TP53 gene (p53) are among the most frequent and important events. Because of its importance, many aspects of TP53 have been studied, including preneoplastic lesions and TP53 as a marker for early detection and prognosis and as a therapeutic option. We summarize recent knowledge of TP53 in lung cancer with a special emphasis on the relationship between smoking exposure (e.g, cigarette, etc.) and specific mutational pattern of TP53 by analyzing the latest version of the International Agency for Research on Cancer (IARC) database on TP53 mutations in human cancer. Our analysis confirmed several other studies showing significant differences in the frequencies of G:C to T:A transversions between ever-smokers and never-smokers. Furthermore, when comparing the mutational spectrum by gender, important differences were noted between male and female never smokers. We concluded that the previously noted G:C to T.A transversions were mainly due to female smokers having a high frequency of these changes compared to female never smokers. There was no relationship between adenocarcinomas and squamous cell carcinomas independent of gender. We also examined the seven codons which have been previously identified as hot spots, that is, the sites of frequent G:C to TA transversions in smoking,related lung cancers. However, there was no specific codon which was strongly related to smoke exposure despite a moderate relationship. We considered the term "warmspot" may be more appropriate. While mutations of TP53 are frequent in lung cancers, further investigation is necessary to understand their role for lung carcinogenesis, especially as they relate to gender differences, and to translate our laboratory knowledge to clinical applications.
引用
收藏
页码:229 / 239
页数:11
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