The p53 mutations in colorectal, esophageal and lung carcinomas from Hong K
ong were studied previously. The availability of mutation data for these ca
ncers in one geographical region prompted investigations into special featu
res of these p53 alterations. Mutations in codons 175, 176, 248 and 273 acc
ounted for 35% of all mutations detected. A hot spot at codon 176 observed
in esophageal carcinomas was not detected in any of the other aerodigestive
tract tumors studied and appeared to be uniquely restricted to Chinese eso
phageal cancers. Other unique mutation sites, and a notably higher frequenc
y of insertions and deletions in each of these cancers, were also detected
in Chinese patients as compared to Caucasians.