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      Role of a p53 polymorphism in the development of human papillomavirus-associated cancer.

      Nature
      Alleles, Arginine, metabolism, Carcinoma, Squamous Cell, genetics, virology, DNA-Binding Proteins, Disease Susceptibility, Female, Gene Deletion, Genotype, Heterozygote, Humans, Oncogene Proteins, Viral, Papillomaviridae, physiology, Papillomavirus Infections, Polymorphism, Genetic, Repressor Proteins, Skin Neoplasms, Tumor Suppressor Protein p53, Tumor Virus Infections, Uterine Cervical Neoplasms

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          Abstract

          The E6 oncoprotein derived from tumour-associated human papillomaviruses (HPVs) binds to and induces the degradation of the cellular tumour-suppressor protein p53. A common polymorphism that occurs in the p53 amino-acid sequence results in the presence of either a proline or an arginine at position 72. The effect of this polymorphism on the susceptibility of p53 to E6-mediated degradation has been investigated and the arginine form of p53 was found to be significantly more susceptible than the proline form. Moreover, allelic analysis of patients with HPV-associated tumours revealed a striking overrepresentation of homozygous arginine-72 p53 compared with the normal population, which indicated that individuals homozygous for arginine 72 are about seven times more susceptible to HPV-associated tumorigenesis than heterozygotes. The arginine-encoding allele therefore represents a significant risk factor in the development of HPV-associated cancers.

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