Volume 123, Issue 10 pp. 837-846
Original Article

Leukemia inhibitory factor promotes tumor growth and metastasis in human osteosarcoma via activating STAT3

Bin Liu

Bin Liu

Department of Orthopedics, Liaocheng Second People's Hospital, Linqing City, Shandong Province, China

These two authors contributed equally to this work.Search for more papers by this author
Yi Lu

Yi Lu

Department of Orthopedics, The People's Hospital of Zhangqiu City, Zhangqiu City, Shandong Province, China

These two authors contributed equally to this work.Search for more papers by this author
Jinzhi Li

Jinzhi Li

Department of Pathology, The People's Hospital of Zhangqiu City, Zhangqiu City, Shandong Province, China

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Yanping Liu

Yanping Liu

Department of Pediatric Gastrointestinal Surgery, The People's Hospital of Zhangqiu City, Zhangqiu City, Shandong Province, China

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Jian Liu

Jian Liu

Department of Orthopedics, The People's Hospital of Zhangqiu City, Zhangqiu City, Shandong Province, China

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Weiguo Wang

Corresponding Author

Weiguo Wang

Department of Interventional Radiology, Affiliated Hospital of Jiangnan University and Wuxi 4th People's Hospital, Wuxi City, Jiangsu Province, China

Weiguo Wang, Huihe Road No. 200, Binhu District, Wuxi City, Jiangsu Province 214062, China. e-mail: [email protected]Search for more papers by this author
First published: 14 August 2015
Citations: 27

Abstract

The leukemia inhibitory factor (LIF) has been demonstrated to be an oncogene and participated in multiple procedures during the initiation and progression of many human malignancies. However, the role of LIF in osteosarcoma is still largely unknown. Here, we performed a series of in vitro and in vivo experiments to investigate the expression and biological functions of LIF in osteosarcoma. Compared to that in the non-cancerous tissues, LIF was significantly overexpressed in a panel of 68 osteosarcoma samples (p < 0.0001). Moreover, the overexpression of LIF was significantly correlated with advanced tumor stage, larger tumor size, and shorter overall survival. In addition, knockdown of LIF notably suppressed the proliferation and invasion of osteosarcoma via blocking the STAT3 signal pathway; in contrast, treatment with the recombinant LIF protein significantly promoted the growth and invasion of osteosarcoma through enhancing the phosphorylation of STAT3, which can be partially neutralized by the STAT3 inhibitor, HO-3867. In conclusion, we demonstrated that LIF was frequently overexpressed in osteosarcoma, which could promote the growth and invasion through activating the STAT3 pathway. Our findings proposed that LIF might be a potent therapeutic target for osteosarcoma.

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