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Uncoupling Protein 2 (UCP2) and p53 Expression in Invasive Ductal Carcinoma of Breast
- Source :
- The Korean Journal of Pathology. 44:565
- Publication Year :
- 2010
- Publisher :
- The Korean Society of Pathologists and The Korean Society for Cytopathology, 2010.
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Abstract
- Background : Uncoupling protein 2 (UCP2) is a recently identified mitochondrial inner membrane anion carrier and a negative regulator of reactive oxygen species production. In this study, we evaluated the characteristics and relationships of UCP2 and p53 expression in breast cancer tissues. Methods : Tissue microarray slides from 107 cases of invasive ductal carcinoma of the breast were constructed, UCP2 and p53 immunohistochemical staining was conducted, and clinicopathological correlations were investigated. Results : UCP2 expression in invasive ductal carcinoma was high in 53 cases (49.5%), while p53 expression in invasive ductal carcinoma was high in 37 cases (34.6%). UCP2 expression was correlated significantly with histological grade (p = 0.038) and mitotic count (p = 0.050). UCP2 expression was correlated significantly with p53 expression in invasive ductal carcinoma of the breast (p = 0.045). UCP2 expression (p = 0.8308) and p53 expression (p = 0.3292) showed no significant difference for the overall survival rate in patients with invasive ductal carcinoma. Conclusions : UCP2 expression in invasive ductal carcinoma increased proportionally with histological grade and mitotic count. High UCP2 expression in invasive ductal carcinoma was observed in conjunction with high p53 expression.
- Subjects :
- Pathology
medicine.medical_specialty
Tissue microarray
business.industry
medicine.disease
Invasive ductal carcinoma
Mitotic Count
Pathology and Forensic Medicine
Breast cancer
Uncoupling protein 2
Cancer research
Medicine
Immunohistochemistry
skin and connective tissue diseases
business
Inner mitochondrial membrane
P53 expression
Subjects
Details
- ISSN :
- 17381843
- Volume :
- 44
- Database :
- OpenAIRE
- Journal :
- The Korean Journal of Pathology
- Accession number :
- edsair.doi...........b828494133675e00061399f12ece2a78