Expressions of breast cancer resistance protein, cytokeratin-8, and chromogranin-A in human breast carcinoma tissue: Is there a correlation with multi-lineage potential of bone marrow mesenchymal stem cells?
10.3969/j.issn.1673-8225.2010.01.013
- VernacularTitle:人乳腺病变组织乳腺癌耐药蛋白及细胞角蛋白8和嗜铬蛋白A的表达:可能与多向分化潜能干细胞相关?
- Author:
Yingxin CHEN
;
Lianhong LI
;
Jie SUN
;
Bo WANG
;
Lixia WANG
- Publication Type:Journal Article
- From:
Chinese Journal of Tissue Engineering Research
2010;14(1):57-62
- CountryChina
- Language:Chinese
-
Abstract:
BACKGROUND: Generally speaking, neuroendocrine cells have been not observed in normal breast tissue but found in breast carcinoma tissue which was affected by local microenvironment and hormone level during differentiation of breast epithelial stem cells.OBJECTIVE: By detecting expressions of breast cancer resistance protein (BCRP), cytokeratin-8 (CK8), and chromogranin-A (CgA) in breast carcinoma tissue, to explore the possible mechanism of neuroendocrine cells observed in breast carcinoma tissue during differentiation of multi-lineage potential of bone marrow mesenchymal stem cells.METHODS: BCRP, CK8, and CgA were used as markers for SP stem cells, glandular epithelium differentiation, and neuroendocrine differentiation, respectively. Immunohistochemistry was used to detect the expressions of BCRP, CK8, and CgA in breast tissues of 89 subjects and analyze their correlation. RESULTS AND CONCLUSION: Both BCRP and CK8 expressions were observed in normal breast tissues, hyperplastic tissues, and breast carcinoma tissue. BCRP expression was increased in the breast carcinoma tissue; CK8 expression was decreased with the abnormal differentiation of breast tissue; CgA expression was only detected in breast carcinoma tissue. BCRP expression was significantly correlated with positive CgA expression (P < 0.01), but it was no correlation with positive CK8 expression in normal breast tissues, hyperplastic tissues, and breast carcinoma tissue (P=0.069). The results suggested that neuroendocrine cells were not observed in both normal breast tissues and hyperplastic tissues but in breast carcinoma tissue, which possibly correlated to differentiation of multi-lineage potential of bone marrow mesenchymal stem cells.
