CXCR1/Akt signaling activation induced by mesenchymal stem cell-derived IL-8 promotes osteosarcoma cell anoikis resistance and pulmonary metastasis

• Published in: Cell death & disease Vol. 9; no. 7; pp. 714 - 11
• Main Authors: Du, Lin, Han, Xiu-guo, Tu, Bing, Wang, Min-qi, Qiao, Han, Zhang, Shu-hong, Fan, Qi-ming, Tang, Ting-ting
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 18-06-2018; Springer Nature B.V
• Subjects: 13/1; 13/100; 13/109; 13/2; 13/21; 13/31; 13/44; 13/51; 13/95; 14/5; 59/5; 64/60; 82/80; AKT protein; Anoikis; Antibodies; Apoptosis; Biochemistry; Biomedical and Life Sciences; Bone cancer; Cancer; Cell adhesion; Cell adhesion & migration; Cell Biology; Cell Culture; Immunology; Interleukin 8; Life Sciences; Lung cancer; M cells; Mesenchyme; Metastases; Metastasis; Osteosarcoma; Sarcoma; Signal transduction; Stem cell transplantation; Stem cells
• DOI: 10.1038/s41419-018-0745-0
• EISSN: 2041-4889

The loss of appropriate cell adhesion normally induces apoptosis via a process termed anoikis. The aim of this study was to investigate the effects of mesenchymal stem cells (MSCs) in the cancer microenvironment on the anoikis resistance and pulmonary metastasis of osteosarcoma (OS) cells, and to evaluate the critical role of the interleukin (IL)-8/C-X-C chemokine receptor (CXCR) 1/Akt-signaling pathway in these processes. Metastatic OS subtype cells, which did or did not interact with MSC-conditioned medium (MSC-CM) in vitro, were isolated from the pulmonary site and named Saos2-lung-M. Both MSC-CM and IL-8 treatment increased the anoikis resistance of Saos2 cells in vitro. Moreover, exogenous MSC-CM promoted the survival and metastasis of Saos2 cells in nude mice. Saos2-lung-M cells were more malignant and resistant to anoikis than parental cells. MSCs secreted IL-8, thereby protecting OS cells from anoikis. Blocking the IL-8/CXCR1/Akt pathway via CXCR1 knockdown inhibited the pulmonary metastasis of Saos2-lung-MSCs and prolonged the survival of tumor-bearing mice. In conclusion, MSCs enhanced OS cell resistance to anoikis and pulmonary metastasis via regulation of the IL-8/CXCR1/Akt pathway. These findings suggest that MSCs can “select for” OS cells with high metastatic potential in vivo, and highlight CXCR1 as a key target in the regulation of pulmonary metastasis of OS cells.