A Comparing Study of the Expression Patterns of Vascular Endothelial Growth Factor (VEGF), Proliferating Cell Nuclear Antigen (PCNA), Apoptosis in CIN and Cervical Cancer.
- Author:
Moon Hong KIM
1
;
Noh Hyun PARK
;
In Ae PARK
;
Soon Beom KANG
Author Information
1. Department of Obstetrics and Gynecology, College of Medicine, Seoul National University, Seoul, Korea.
- Publication Type:Original Article
- Keywords:
Cervical cancer;
CIN;
PCNA;
VEGF;
Apoptotic index
- MeSH:
Apoptosis*;
Diagnosis;
In Situ Nick-End Labeling;
Paraffin;
Polymerase Chain Reaction;
Proliferating Cell Nuclear Antigen*;
Seoul;
Uterine Cervical Neoplasms*;
Vascular Endothelial Growth Factor A*
- From:Korean Journal of Obstetrics and Gynecology
2002;45(2):244-250
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
OBJECTIVE: The aim of this study was to identify the relationship between the progression of CIN (cervical intraepithelial neoplasia) to cervical cancer and expression pattern of VEGF, PCNA and apoptosis. METHODS: We prepared forty paraffinized cervical tissue blocks consisting of each 10 CINI, CINII, CINIII, and invasive cervical cancer tissues, which had been already diagnosed histologically in Seoul National University Hospital from July, 1998 to June, 1999. The protein expression of VEGF and PCNA were examined by immunohistochemical staining. We defined PI (positive index) as the percentage of cells that were positive PCNA staining when examined in high power fields with light microscope (x400). We used TUNEL staining to calculate apoptotic index defined as the number of the cells undergoing apoptosis per 1,000 tumor cells. To detect HPV type 16 or 18 from paraffin-embedded tissues, we selected the nested PCR method. RESULTS: The VEGF expression showed significant difference between early cervical lesions (CINI & II) and advanced cervical lesions (CINIII & cancer) (p=0.041). In case of PCNA expression there was no significant difference. When we define positive case as the case of which AI was greater than 5, AI according to each diagnosis showed no difference. In the aspect of HPV infection we could find that there was significant increment of HPV 16/18 infection rate in advanced cervical lesions (CINIII, cervical cancer) comparing with early cervical lesions such as CINI, CINII. CONCLUSION: Our results suggest that the evaluation of VEGF expression and HPV infection is potentially useful for the prediction of the progression of CIN to carcinoma.
