Previously a low frequency of p53 mutations was detected in nasopharyngeal
carcinoma (NPC) using molecular techniques to screen for mutations, yet imm
unohistochemical staining revealed a high frequency of p53 aberrant protein
s. These findings might be attributed to the occurrence of p53 mutations ou
tside the common hot spots and/or the inactivation of the protein through i
nteractions with cellular or viral proteins. Using a previously established
simple and sensitive p53 yeast functional assay, we blindly screened 25 na
sopharyngeal biopsies for p53 mutations from exons 4 to 11, p53 was mutated
in 27.3% of NPC specimens and in 0% of the nasopharyngeal biopsies from pa
tients with non-malignant diseases. Two p53 mutations were detected in exon
7 and two were detected in exon 8. Interestingly, the exon 8 mutations obs
erved in NPC lie in codons which appear to be hot spots for mutations in ot
her head and neck cancers. (C) 1998 Elsevier Science Ireland Ltd. All right
s reserved.