Chinese Journal of Tissue Engineering Research ›› 2016, Vol. 20 ›› Issue (10): 1468-1473.doi: 10.3969/j.issn.2095-4344.2016.10.014

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Biological features of CD90+ tumor stem cells in ovarian cancer

Liu Zhi-hui1, Xiang Zhi-hui2   

  1. 1Wuhan Women and Children Medical Care Center, Wuhan 430016, Hubei Province, China; 2the Central Hospital of Wuhan, Tongji Medical College, Huazhong University of Science & Technology, Wuhan 430000, Hubei Province, China
  • Received:2016-01-25 Online:2016-03-04 Published:2016-03-04
  • About author:Liu Zhi-hui, Studying for master’s degree, Wuhan Women and Children Medical Care Center, Wuhan 430016, Hubei Province, China

Abstract:

BACKGROUND: Thinking from ovarian cancer stem cell theory shows that: in the tumor cells, there are a fraction of stem cells with self-renewing ability and multipotent differentiation, which are the root causes of ovarian cancer recurrence and drug resistance. Studies have shown that CD90 can be used as a surface marker of mesenchymal stem cells and stem cells of other cancers.
OBJECTIVE: To explore the biological features of CD90+ tumor cells from ovarian cancer tissues.
METHODS: Primary ovarian cancer cells were isolated from the abdominal dropsy of ovarian cancer patients to sort CD90+ and CD90- cells using flow cytometry. RT-PCR was used to detect expressions of stem cell-related genes and epithelial to mesenchymal transition-related genes. Cell invasion was observed by Transwell invasion assay, cell proliferation and differentiation observed by clone formation assay, stem cell potential observed by suspension sphere-forming assay, and tumor formation rate observed by in vivo tumorigenicity experiment.
RESULTS AND CONCLUSION: Compared with the CD90- cells, the expressions of CD44, CD133, ALDH1, N-cad and Vimentine were significantly higher in the CD90+ cells (P < 0.05), but the expression of E-cad was significantly decreased in the CD90+ cells (P < 0.05). Tumor formation rates of CD90- and CD90+ cells were increased significantly with the increase of seeded cell number, which was more obvious in CD90+ cells. The number of transmembrane cells, the number of cell clones and the number of suspended spheres were significantly higher in the CD90+ cells than the CD90- cells (P < 0.05). Experimental findings from this study show that CD90+ cells highly express epithelial to mesenchymal transition-related genes and stem cell-related genes, with higher invasion, proliferation and differentiation, in vivo tumorigenicity and potential of stem cells. CD90+ cell separation may be a new method to separate ovarian cancer stem cells.