Chinese Journal of Tissue Engineering Research ›› 2015, Vol. 19 ›› Issue (50): 8062-8066.doi: 10.3969/j.issn.2095-4344.2015.50.005

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Breast cancer stem cells: separation and resistance protein analysis

Guo Meng, Wan Li-xin   

  1. Nanyang City Center Hospital, Nanyang 473009, Henan Province, China
  • Received:2015-10-14 Online:2015-12-03 Published:2015-12-03
  • About author:Guo Meng, Master, Associate chief physician, Nanyang City Center Hospital, Nanyang 473009, Henan Province, China

Abstract:

BACKGROUND: Breast cancer stem cells are relatively special cells in the body, which have the self-renewal and multi-differentiation ability to promote tumor formation and development, and maintain tumor growth for a long-term. Therefore, it is of great significance to analyze the expression of resistance proteins of breast cancer stem cells.
OBJECTIVE: To isolate breast cancer stem cells from human breast cancer tissues, to observe their differentiation and morphology characteristics and to analyze their resistance proteins.
METHODS: Thirty tumor samples of breast invasive ductal carcinoma were selected to separate single cell suspension using mechanical separation method, and breast cancer stem cells and differentiated cells were sorted with two-step immunomagnetic bead method. Two-step immunocytochemistry method was used to detect the expression of resistance proteins in breast cancer stem cells.
RESULTS AND CONCLUSION: Percentage of breast cancer stem cells had no significant correlations with age, long diameter of the tumor, lymph node metastasis and histological grading (P > 0.05). P-gp and GST-π positive rates in the breast cancer stem cells were significantly higher than those in the differentiated cells (P < 0.05); while TopoII and LRP positive rates in the breast cancer stem cells were significantly lower than those in the differentiated cells (P < 0.05). To conclude, breast cancer stem cells show stronger drug resistance than the differentiated cells by highly expressing P-gp and GST-π and lowly expressing TopoII and LRP, which may be the key reason for chemotherapy resistance in breast cancer. 

 

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