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Background and Objective: Breast cancer is one of the most important malignant tumors world -wide and the second common cancer in the females. Breast cancer is associated with a number of environmental factors and genetic damages. Ki67 is a proto-oncogene which is activated in cell proliferation process. Ki67 is important in prognosis and response to chemotherapy. The aim of this study was to investigate the Ki67 gene expression in patients with breast cancer by immunohistochemistry method. Materials and Methods: This descriptive laboratory study was conducted on 80 breast cancer specimens from patients admitted to the hospitals in Sabzevar, Iran during 2005-09. Samples were fixed in formalin, the tissue processing was done and sections were stained by Hematoxilin and Eosin method. The malignancy was diagnosed by two pathologists blindly. Over expression of ki67 was determined with the immunohistochemistry method. Slides were scored into negative, weak, average and strong based on percentage of cells which were stained. The Data were analyzed by SPSS-11.5, Chi-Square and Fisher’s exact tests. Results: Ki67 proliferative marker was observed in 37 (46.3%) specimens with breast cancer. Sensivity of staining was one positive (+) in 15 cases, two positive (++) in 14 cases and three positive (+++) in 8 cases. There was a significant relationship between Ki67 gene expression and tumor type and tumor staging (P<0.05), but there was no significant relationship between Ki67 gene expression and tumor grade. Conclusion: It is concluded that, ki67 is expressed mostly in invasive and developed breast cancer.

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Background and Objective: Antiepileptic drugs can partiality control or achieve the convulsion. There are controversial issues about the use and effect of ethanol to control epileptic convulsion seizers. This study was done to determine the effect of ethanol on microvascular alterations in the brain cortex of epileptic mice treated by valporic acid (VPA). Materials and Methods: In this experimental study, 36 BALB/c mice were allocated randomly into six groups including: 1-PTZ (Pentylenetetrazol), 2- Ethanol, 3- VPA+ PTZ, 4- ethanol + PTZ, 5-ethanol+ VPA+ PTZ and control groups. The animal brains were excluded and stained by Hematoxilin and eosin. Thirty-six optical microscopic field from each group were selected and microvascular count were determined. Immunohistochemical method was used for detection of injuries in the vascular brain tissue. Results: Mean number of brain microvascular cortex significantly increaed in PTZ+ethanol and PTZ+ethanol+VPA groups in compare to controls (P<0.05). Infiltration and thrombophlebitis were observed in vessels and cortical brain tissues in mice which received ethanol and PTZ. Proliferations in endothelial vascular cells were seen in PTZ and VPA+ethanol groups. Immunohistochemical method showed the endothelial cells of PTZ+ethanol groups were more stained in compare to the other experimental groups. Conclusion: Ethanol + PTZ cause cellular infiltration and damage to the cortical brain vessels although VPA reduces histological altheretions.