| Literature DB >> 29725446 |
Baobiao Zhuo1,2, Yuan Li2, Feng Gu3, Zhengwei Li2, Qingzeng Sun2, Yingchun Shi2, Yang Shen2, Fengfei Zhang2, Rong Wang4, Xiaodong Wang1.
Abstract
The rapid development of metastatic lesions remains the leading cause of mortality for patients with osteosarcoma. CD155 serves a key role in cancer cell migration, invasion and metastasis. However, the function and mechanism of CD155 has not been explored in osteosarcoma metastasis. In the present study, we found that CD155 was significantly upregulated in lung metastatic tissue and the highly metastatic cell line K7M2-WT (K7M2) of osteosarcoma. Overexpression of CD155 in K7M2 cells enhanced lung metastasis, while inhibition of CD155 by an anti-CD155 monoclonal antibody reduced metastasis. Blocking of CD155 also decreased migration and invasion of K7M2 cells in vitro. A western blot analysis revealed that blocking of CD155 inhibits metastasis by downregulating focal adhesion kinase (FAK) and phosphorylated FAK (pFAK) in osteosarcoma. The results revealed that CD155 serves a crucial role in the metastasis of osteosarcoma by regulating FAK and may provide a novel molecular target for therapeutic intervention in metastatic osteosarcoma.Entities:
Keywords: CD155; invasion; metastasis; migration; osteosarcoma
Year: 2018 PMID: 29725446 PMCID: PMC5920504 DOI: 10.3892/ol.2018.8228
Source DB: PubMed Journal: Oncol Lett ISSN: 1792-1074 Impact factor: 2.967