Journal List > J Breast Cancer > v.10(1) > 1036069

Son, Woo, Sohn, Bae, Lee, Kang, Kim, Baek, Lim, Lee, Lee, Kim, Kim, Min, Oh, Kim, Kim, and Cho: Prognostic Value of Apoptosis and the Survivin, bcl-2, and p53 Expressions in Breast Cancer Patients

Abstract

Purpose

Survivin is a member of the inhibitor of apoptosis (IAP) protein family, and it is involved in the regulation of cell division. The over-expression of survivin has been reported to be associated with the parameters for a poor prognosis in most human cancers, including lung, breast, colon, stomach, esophagus, pancreas, etc. In this study, we examined the expression of a member of a novel IAP protein family, survivin, in breast cancer and its association with tumor cell apoptosis and the overall prognosis.

Methods

80 cases of formalin-fixed paraffin-embedded breast cancer tissue were immunostained with, using polyclonal survivin (Novus Biologicals, Littleton, USA), monoclonal bcl-2 (DAKO, Carpinteria, USA), and monoclonal p53 antibodies (DAKO, Carpinteria, USA). The histochemical method used for the analysis of apoptosis was based on ApopTag® Peroxidase In Situ OligoLigation (ISOL) Apoptosis Detection Kit (CHEMICON International Inc. Temecula, USA).

Results

Immunohistochemical analysis showed that cytoplasmic survivin expression was positive in 43 of 80 cases (53.8%) of breast carcinomas and it was positive for 70% of the cases that showed a bcl-2 expression tumors. Statistical analysis revealed that the survivin expression was correlated with lymph node metastasis, the tumor stage, and the histological grade. Although the survivin expression was not correlated with p53 mutations, the survivin positive cases were associated with a bcl-2 expression (p=0.015) and a reduced apoptotic index (p=0.024). On the Cox proportional hazard model analysis, the apoptotic index was not identified as a significant independent predictor of overall survival (p=0.072), although the patients with a low apoptotic index (<0.2%) had a worse survival rates than those patient in the group with a high apoptotic index (≥0.2%).

Conclusion

The results suggest that apoptosis inhibition of apoptosis by survivin may be a prognostic parameter for a worse outcome in breast carcinoma patients.

Figures and Tables

Fig 1
Immunohistochemical examination for survivin. (A) The tumor cells of infiltrating ductal carcinoma show positive reaction in survivin (×100). (B) The cytoplasm of atypical cells in moderate epithelial hyperplasia shows strong positive reaction in survivin (×100). (C) The metastatic tumor cells of infiltrating ductal carcinoma lymph node show positive reaction in survivin (×100).
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Fig 2
Histochemical staining for bcl-2 and apoptotic tumor cells. (A) bcl-2 expression in breast cancers (×40). (B) in situ oligiligation reaction (ISOL) for apoptosis (arrows: ×200).
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Fig 3
Kaplan-Meier survival curve according to cytoplasmic survivin expression (A) and high vs. low Apoptotic Index (B).
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Table 1
General characteristics of patients
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ER=estrogen receptor.

Table 2
Cytoplasmic survivin expression in breast carcinoma
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*: p<0.05 (control vs. atypical hyperplasia, primary cancer, malignant lymph node).

Table 3
Correlation between clinicopathological factors and expression of survivin, bcl-2 in breast cancer (n=80)
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ER=estrogen receptor.

Table 4
Expression of bcl-2 and p53 in survivin positive breast cancer
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Table 5
Correlation between clinicopathological factors and Apototic Index in breast cancer
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AI=apoptotic index; ER=estrogen receptor.

Table 6
Cox proportional hazard model analysis
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CI=confidence interval; ER=estrogen receptor; AI=apoptotic index.

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