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Oncol Rep ; 15(4): 949-56, 2006 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-16525684

RESUMO

The study investigated an association between the germline polymorphism at TP53 codon 72 and the development of papillary thyroid cancer (PTC) following exposure to radiation from the Chernobyl accident. TP53 genotype was examined in 48 pediatric/adolescent (age at diagnosis <18 years) and 68 adult post-Chernobyl patient with PTC, 53 adult patients with sporadic PTC and 313 healthy individuals from Russian-Ukrainian population. In addition, we evaluated loss of heterozygosity for TP53 and the allele expression ratio. The genotype of the patients was correlated with clinicopathological data. Arg TP53 homozygotes were found to be significantly underrepresented among adults with post-Chernobyl PTC, but not in children and adolescents when compared with sporadic PTC cases and the general population. In the tumors, cell transformation did not lead to allelic loss or biased TP53 allele expression in heterozygous individuals. None of TP53 genotypes specifically associated with tumor stage and morphology, however there were particular correlations with lymph node status in certain age groups of radiation-associated cases not seen in sporadic PTCs. The findings suggest TP53 allele combinations other than Arg/Arg may contribute to the risk of development of PTC in individuals exposed to radiation during their late childhood, adolescence or in young adulthood.


Assuntos
Carcinoma Papilar/patologia , Neoplasias Induzidas por Radiação/patologia , Polimorfismo Genético/genética , Neoplasias da Glândula Tireoide/patologia , Proteína Supressora de Tumor p53/genética , Adolescente , Adulto , Idoso , Alelos , Sequência de Bases , Carcinoma Papilar/genética , Criança , Pré-Escolar , Códon/genética , Feminino , Regulação Neoplásica da Expressão Gênica , Frequência do Gene , Genótipo , Humanos , Lactente , Recém-Nascido , Perda de Heterozigosidade , Metástase Linfática , Masculino , Pessoa de Meia-Idade , Mutação de Sentido Incorreto/genética , Mutação de Sentido Incorreto/efeitos da radiação , Estadiamento de Neoplasias , Neoplasias Induzidas por Radiação/genética , Polimorfismo Genético/efeitos da radiação , Neoplasias da Glândula Tireoide/genética
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