骨肉瘤
白血病抑制因子
癌症研究
车站3
癌基因
体内
转移
白血病
基因敲除
癌症
医学
磷酸化
化学
生物
细胞培养
内科学
细胞周期
细胞因子
细胞生物学
白细胞介素6
生物技术
遗传学
作者
Bin Liu,Yi Lu,Jinzhi Li,Yanping Liu,Jian Liu,Weiguo Wang
出处
期刊:Apmis
[Wiley]
日期:2015-08-14
卷期号:123 (10): 837-846
被引量:32
摘要
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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