Aims: Cyclin D1 overexpression was examined in early gastric carcinomas and
precursor lesions with the following aims; (1) to assess the chronology of
cyclin D1 overexpression in various stages of gastric carcinogenesis, (2)
to correlate cyclin D1 overexpression with the Lauren type, the grade of di
fferentiation and the type of growth pattern of the tumours and (3) to corr
elate cyclin D1 overexpression with clinical parameters, in particular lymp
h node metastasis and overall prognosis.
Methods and results: Forty-five paraffin-embedded gastrectomy specimens fro
m early carcinomas were examined for the presence of various precursor lesi
ons. The Lauren type, the grade of differentiation and the type of growth p
attern were reassessed for all early carcinomas. Cyclin D1 overexpression w
as examined using the monoclonal antibody DCS-6, Cyclin D1 overexpression w
as absent from all precursor lesions. Ten early carcinomas (22%) were cycli
n D1 positive without significant differences when stratified according to
Lauren type, grade of differentiation, type of growth pattern or lymph node
status. Univariate analysis failed to show a significant difference in 5-y
ear survival rate between cyclin D1 positive and negative early carcinomas
(90% vs, 94%),
Conclusions: Cyclin D1 protein overexpression does not play a role in the p
rogression from normal to neoplastic gastric mucosa and does not discrimina
te between intestinal and diffuse type early gastric carcinomas of Caucasia
n origin. Moreover, mechanisms other than cyclin D1 protein overexpression
underlie the reported difference in biological behaviour of early gastric c
arcinomas with different types of growth pattern. Finally, although it appe
ars that cyclin D1 does not have prognostic significance, studies on larger
numbers, including advanced carcinomas, are warranted.