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p53 codon 72 polymorphisms in human papillomavirus-negative and human papillomavirus-positive squamous cell carcinomas of the oropharynx

โœ Scribed by Federica Perrone; Luigi Mariani; Elisa Pastore; Marta Orsenigo; Simona Suardi; Barbara Marcomini; Luca DaRiva; Lisa Licitra; Antonino Carbone; Marco A. Pierotti; Silvana Pilotti


Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
81 KB
Volume
109
Category
Article
ISSN
0008-543X

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โœฆ Synopsis


Abstract

BACKGROUND.

Tobacco smoking, alcohol abuse, and highโ€risk human papillomavirus (HPV) are risk factors in the etiology of oropharyngeal squamous cell carcinomas (SCCs). The TP53 polymorphism, in which an arginine (R) is changed to proline (P) at codon 72, is functionally significant and could therefore be a predisposing genetic defect.

METHODS.

The aim of the study was to investigate the role of codon 72 polymorphism by means of double gradientโ€denaturing gel electrophoresis in 77 oropharyngeal SCC patients including 33 TP53 mutated and 16 HPVโ€16โ€positive cases. The controls consisted of 141 consecutive healthy blood donors.

RESULTS.

The cases and controls showed significantly different genotype distribution (P = .0005): the frequencies of the RR, RP, and PP genotypes among the cases were, respectively, 81.8%, 10.4%, and 7.8%, as opposed to 59.6%, 33.3%, and 7.1% among the controls, in agreement with the Hardyโ€Weinberg equilibrium (P = .35). The PP genotype was significantly overrepresented among females (22.2% vs 3.4%; P = .0243) and in HPVโ€16โ€positive cases (25.0% vs 3.3%; P = .0152). No segregation was found between either of the codon 72 genotypes and age or TP53 mutations.

CONCLUSIONS.

The significantly lower frequency of the RP genotype in the patients as a whole suggests that it has a protective effect on oropharyngeal SCCs. Moreover, the PP genotype may be a risk factor for the development of oropharyngeal SCC by females and the development of HPVโ€16โ€related SCC, although the findings need to be validated in a larger number of tumors. Cancer 2007. ยฉ 2007 American Cancer Society.


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