Wg. Mccluggage et al., High metallothionein expression is associated with features predictive of aggressive behaviour in endometrial carcinoma, HISTOPATHOL, 34(1), 1999, pp. 51-55
Citations number
28
Categorie Soggetti
Research/Laboratory Medicine & Medical Tecnology","Medical Research Diagnosis & Treatment
Aims: Metallothioneins (MTs) are a group of ubiquitous low molecular weight
proteins with a high affinity for heavy metal ions. The aim of the present
study was to investigate MT expression in a series of endometrial carcinom
as. We wished to determine whether MT expression in endometrial carcinoma w
as related to established prognostic factors such as tumour grade, stage an
d histological type. We also wanted to establish if high MT expression in c
urettings of endometrial carcinoma was predictive of high expression in the
subsequent hysterectomy specimen,
Methods and Results: Sixty-three cases of endometrial carcinoma were includ
ed in the study, These comprised 57 endometrioid adenocarcinomas (15 grade
1, 25 grade 2, 17 grade 3), three papillary serous adenocarcinomas, two muc
inous adenocarcinomas and one clear cell adenocarcinoma. Forty-five tumours
were stage I, 10 were stage II and eight were stage III. In 28 cases, diag
nostic endometrial curettings, performed prior to hysterectomy, were availa
ble for study. Immunohistochemical staining was performed using the anti-MT
monoclonal antibody E9. The intensity and distribution of MT staining were
assessed using a semiquantitative method. This resulted in an intensity di
stribution (ID) score out of a maximum of 300. The mean ID score of grade 1
and 2 endometrioid adenocarcinomas was 67 and 63, respectively, while for
grade 3 tumours the mean ID score was 114. This was statistically significa
nt (P = 0.05). The three papillary serous adenocarcinomas had high ID score
s with a mean of 208. The mean ID score of stage I tumours was 69, This was
lower than those of stage II and LII tumours which had mean ID scores of 1
16 and 128, respectively. However, these differences were not statistically
significant (P = 0.288). A significant correlation was observed between MT
ID scores in endometrial curettings and in the subsequent hysterectomy (P
= 0.013).
Conclusions: MT isoforms can be demonstrated in most endometrial adenocarci
nomas. High MT ID scores are associated with high grade and high stage endo
metrial adenocarcinomas and with the aggressive papillary serous adenocarci
noma, Whether this is of value as an independent prognostic factor has yet
to be established.