Korean J Pathol.
2000 Apr;34(4):280-287.
Expression of bcl-2 and p53 Protein in Premalignant Lesion and Invasive Squamous Cell Carcinoma of the Uterine Cervix
- Affiliations
-
- 1Departments of Pathology, Keimyung University School of Medicine, Taegu 700-712, Korea.
- 2Departments of Obstetrics and Gynecology, Keimyung University School of Medicine, Taegu 700-712, Korea.
- 3Departments of Pathology, Institute for Medical Science, Keimyung University School of Medicine, Taegu 700-712, Korea.
Abstract
-
In order to understand the possible involvement of bcl-2 and p53 proteins in the
tumorigenesis of the cervical cancer and precancerous lesion, we studied the expression patterns of
bcl-2 and p53 proteins in 25 cases of carcinoma in situ, 12 cases of microinvasive cervical
carcinoma, and 37 cases of invasive cervical carcinoma, respectively. By immunohistochemistry,
76% of in situ carcinoma, 83.3% of microinvasive cervical carcinoma, and 60.9% of invasive
cervical carcinoma were positive for bcl-2, while the staining of basal cell layers, columnar cells,
and squamous metaplastic epithelium of normal cervical epithelium were positive for bcl-2 in
91.9%, 73.1%, and 81.8% of cases, respectively. Furthermore, two out of fourteen cases of invasive
cervical carcinoma with lymph node metastasis were positive for bcl-2. p53 was expressed in
72.7% of condyloma or dysplasia, 12% of in situ carcinomas, 33.3% of microinvasive cervical
carcinoma, and 43.5% of invasive cervical carcinomas without metastasis. Six out of fourteen cases
of invasive cervical carcinoma with lymph node metastasis were positive for p53 immunostaining.
In contrast, 5.4% of basal cells and 9.1% of squamous epithelium, and none of the columnar cells
in normal cervical epithelium were positive for p53. In summary, the bcl-2 protein was highly
expressed in the proliferative lesion of reserve cells, such as normal reserve cells, columnar cells,
squamous metaplasia, carcinoma in situ, and microinvasive squamous cell carcinoma. p53
expression was increased in condyloma, carcinoma in situ, and invasive carcinoma where the
reserve cells were non-proliferative. Based on these findings, we propose that bcl-2 and p53
protein are involved in the development and progression of uterine cervical carcinoma.