Chinese Medical E-ournals Database

Chinese Journal of Obstetrics & Gynecology and Pediatrics(Electronic Edition) ›› 2008, Vol. 04 ›› Issue (03): 186 -190. doi: 10.3877/cma.j.issn.1673-5250.2008.03.105

Original Article

A Study on the Expression and Clinical Significance of AIB1 Protein in Ovarian Borderline Epithelial Tumor

Xiao-yan HAN, Yue CHEN, Min-min HOU, Jian ZHANG, Xiao-li WAN, Kai-xuan YANG, Ming-rong QIE   

  1. Department of Obstetrics and Gynecology, West China Second Hospital, Sichuan University, Chengdu 610041, China
  • Published:2008-06-01
  • Supported by:
    * Project No. 20060610080, supported by the Specialized Research Fund for the Doctoral Program of Higher Education
Objective

To investigate the expression and clinical significance of AIB1(amplified in breast cancer 1) protein in ovarian borderline epithelial tumor.

Methods

We examined the AIB1 expression levels and its relations to clinicopathological features in 24 normal ovaries, 24 cases of ovarian benign epithelial tumor, 18 cases of ovarian borderline epithelial tumor and 69 cases of epithelial ovarian cancer by immunohistochemical method SP. We also simultaneously examined the expression of estrogen receptor (ER), progesterone receptor(PR), p53 protein and bcl-2 protein in ovarian borderline epithelial tumors.

Results

①The positive expression rate of AIB1 protein in ovarian borderline epithelial tumors was 38.89%, which was significantly lower than that in ovarian cancers (65.22%), higher than that in normal ovaries(8.33%), but the difference between the borderline and benign ovarian tumors was not significant. ②The expression of AIB1 protein in clinical stageⅡ~Ⅲ was higher than that in stageⅠ, but the expression levels in different histological groups were not significant. ③AIB1 protein expression was positively correlated with estrogen receptor, progesterone receptor, p53 protein, but there was no correlation between expressions of AIB1 and bcl-2 protein.

Conclusion

The expression of AIB1 may play a role in the ovarian carcinogenesis of the borderline epithelial tumor through steroid receptor and mutational p53 protein signal transduction pathways.

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