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Gynaecology. Apoptosis and the expression of Bax and Bcl-2 in hyperplasia and adenocarcinoma of the uterine endometrium

BACKGROUND: Apoptosis plays a crucial role in carcinogenesis in various tumours. This study was designed to investigate the occurrence of apoptosis and the expression of Bcl-2 and Bax proteins in endometrial tumours of corpus uteri. METHODS: Endometrial tissues were obtained from 20 patients with en...

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Bibliographic Details
Published in:Human reproduction (Oxford) 2001-10, Vol.16 (10), p.2211
Main Authors: Kokawa, Katsuji, Shikone, Toshihiko, Otani, Tsutomu, Nishiyama, Rika, Ishii, Yuki, Yagi, Shigetaka, Yamoto, Mareo
Format: Article
Language:English
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Summary:BACKGROUND: Apoptosis plays a crucial role in carcinogenesis in various tumours. This study was designed to investigate the occurrence of apoptosis and the expression of Bcl-2 and Bax proteins in endometrial tumours of corpus uteri. METHODS: Endometrial tissues were obtained from 20 patients with endometrioid adenocarcinoma, 16 patients with endometrial hyperplasia, and 4 patients with myoma uteri (which were used as controls). The occurrence of apoptosis was examined by using molecular biochemical techniques. The expression of Bcl-2 and Bax proteins was also investigated using immunohistochemical staining with appropriate antibodies. RESULTS: The labelling of DNA in situ indicated that apoptotic cells were sporadically seen in postmenopausal endometrium (5.2 + or - 2.1, n = 4) and endometrial hyperplasia without atypia (2.6 + or - 0.5, n = 9). In contrast, labelled cells were detected in atypical endometrial hyperplasia (15.9 + or - 2.2, n = 7), and their numbers increased intensely in adenocarcinoma (29.3 + or - 3.7, n = 20). Autoradiographic analysis revealed DNA laddering in many cases of carcinoma. Bcl-2 was highly immunopositive in hyperplasia without atypia (36.2 + or - 6.5%, n = 9), but was decreased in the atypical endometrial hyperplasia (16.3 + or - 4.8%, n = 7). Large fractions of the carcinoma (6.3 + or - 1.8%, n = 20) and normal endometrium (2.8 + or - 1.4%, n = 4) were immunonegative or slightly immunopositive to Bcl-2. In contrast, Bax immunoreactivity was more frequent and stronger in adenocarcinoma (43.6 + or - 4.1%, n = 20) than that in normal endometrium (17.6 + or - 6.7%, n = 4) and hyperplasia (7.2 + or - 2.2%, n = 16). CONCLUSIONS: These results suggest that cells in hyperplasia expressing Bcl-2 might have prolonged survival ability. Neoplastic cells in adenocarcinoma might show apoptosis in association with a decreased expression of Bcl-2 and an increased expression of Bax. Therefore, the frequency of apoptosis and the expression of Bcl-2 and Bax might be correlated with carcinogenesis in the uterine endometrium of humans.
ISSN:0268-1161
1460-2350