K. Hasegawa et al., PRODUCTION AND CHARACTERIZATION OF A MONOCLONAL-ANTIBODY (MSN-3) FOR UTERINE ENDOMETRIAL AND ENDOCERVICAL ADENOCARCINOMA, International journal of oncology, 11(4), 1997, pp. 749-756
A monoclonal antibody (MSN-3) was raised using HEC-108 cells derived f
rom poorly differentiated endometrial carcinoma as the immunogen. The
immunoglobulin subclass of MSN-3 was IgGr1. The target antigen of MSN-
3 was a protein with a molecular weight of 77 kDa, and it was shown to
be localized in the cytoplasm. MSN-3 only reacted with 14% of normal
proliferative endometrium cells, but it showed a high positivity rate
of 66% for endometrial carcinoma. The target antigen of MSN-3 increase
d as endometrial cells became more malignant, and the possibility of c
hanges in localization was also suggested. Moderately and poorly diffe
rentiated endometrial carcinoma showed a high positivity rate for MSN-
3. MSN-3 reacted rarely or not at all with normal cervical glandular t
issue, but the positivity rate for cervical adenocarcinoma (especially
endocervical adenocarcinoma) was a high rate of 59%. The patterns of
staining of endocervical adenocarcinoma by MSN-3 included diffuse stai
ning of the whole cytoplasm and not only that near the glandular lumen
, as well as staining of the basal cytoplasm. Changes in the localizat
ion of the target antigen were clearly associated with carcinogenesis
of the cervical glandular cells. The MSN-3-positive rate was high in p
atients with lymph node metastasis and vascular invasion. Among the st
aining patterns, the basal and diffuse patterns tended to increase wit
h malignacy. The basal pattern of staining was characteristic of MSN-3
, suggesting that it might assist in the diagnosis of cervical adenoca
rcinoma.