Extracellular 5'-nucleotidase (CD73) promotes human breast cancer cells growth through AKT/GSK-3β/β-catenin/cyclinD1 signaling pathway.
Jiangang YuXue WangQi LuJigang WangLuying LiXiaohong LiaoWei ZhuLei LvXiuling ZhiJerry YuYiting JinQiang ZouZhouluo OuXiuping LiuPing ZhouPublished in: International journal of cancer (2017)
To identify the role and to explore the mechanism of extracellular 5'-nucleotidase (CD73) in human breast cancer growth, CD73 expression was measured firstly in breast cancer tissues and cell lines, and then interfered with or over-expressed by recombinant lentivirus in cell lines. Impacts of CD73 on breast cancer cell proliferation and cell cycle were investigated with colony formation assay, CCK-8 and flow cytometry. The relationship between CD73 and AKT/GSK-3β/β-catenin pathway was assessed with adenosine, adenosine 2A receptor antagonist (SCH-58261), adenosine 2A receptor agonist (NECA), CD73 enzyme inhibitor (APCP) and Akt inhibitor (MK-2206). Moreover, the effect of CD73 on breast cancer growth in vivo was examined with human breast cancer transplanting model of nude mice. The results showed that the expression of CD73 was high in breast cancer tissues and increased with advanced tumor grades and lympho-node status. CD73 expression was higher in more malignant cells, and CD73 overexpression promoted breast cancer cell proliferation in both in vivo and in vitro. It activated AKT/GSK-3β/β-catenin/cyclinD1 signaling pathway through CD73 enzyme activity and other mechanism.
Keyphrases
- cell proliferation
- signaling pathway
- cell cycle
- pi k akt
- endothelial cells
- nk cells
- induced apoptosis
- gene expression
- epithelial mesenchymal transition
- poor prognosis
- type diabetes
- breast cancer cells
- metabolic syndrome
- flow cytometry
- lymph node
- insulin resistance
- adipose tissue
- mass spectrometry
- skeletal muscle
- cell cycle arrest
- atomic force microscopy
- protein kinase