Aims: The presence of lysozyme protein in some gastric adenomas and ad
enocarcinomas has been well documented, There have been relatively few
studies investigating the presence of lysozyme in tumours of the larg
e intestine and they show contrasting results, We aim to investigate t
he cellular source and expression of lysozyme in colonic adenomas and
adenocarcinomas. Methods and results: We randomly selected 29 and 27 c
olonic adenomas and adenocarcinomas, respectively, Using in-situ hybri
dization (ISH) and immunohistochemistry (MC), we found an up-regulatio
n of lysozyme in the dysplastic epithelium of all the adenomas studied
, with more than 80% of cases expressing moderate to strong signals, A
lthough the up-regulation of lysozyme was also observed in adenocarcin
omas, only 30% of the cases showed moderate to strong signals, mostly
with an uneven distribution, Down-regulation of lysozyme in the severe
ly dysplastic and invasive foci were noted in some cases of adenoma wi
th malignant transformation. Normal colonic glands were consistently n
egative for lysozyme at both the mRNA and the protein level, but infla
med and immature regenerative colonic epithelium at the crypt base sho
wed positive signals in a similar pattern to those observed in the dys
plastic epithelium of the adenomas. Conclusions: Our results confirm t
hat colonic epithelium can produce lysozyme and its expression is up-r
egulated in the dysplastic epithelium in adenomas and in invasive canc
er cells. It is interesting that regenerative colonic epithelium showe
d a similar pattern of lysozyme expression as in adenomas, The loss of
lysozyme secreting phenotype in most of the invasive tumours suggests
that lysozyme may not confer an advantage to tumour progression.