索拉非尼
肝细胞癌
上皮-间质转换
转移
癌症研究
医学
肿瘤科
细胞
癌症
内科学
生物
遗传学
作者
Yanmin Xu,Huailong Xu,Mingyuan Li,Hua Wu,Yan-He Guo,Jun Chen,Juanjuan Shan,Xuejiao Chen,Junjie Shen,Qinghua Ma,Jingxia Liu,Meiling Wang,Wenxu Zhao,Juan Hong,Yanan Qi,Chao Yao,Qianzhen Zhang,Zhi Yang,Cheng Qian,Jian‐Ming Li
标识
DOI:10.1016/j.canlet.2019.03.049
摘要
Patients with advanced hepatocellular carcinoma (HCC) will almost always develop acquired tolerance after sorafenib therapy, and the molecular mechanism of sorafenib tolerance remains poorly characterized. Here, using our established sorafenib-resistant HCC cell and xenograft models, we identified a novel gene, KIAA1199, which was markedly elevated among the differentially expressed genes involved in sorafenib tolerance. Moreover, elevated expression of KIAA1199 was positively correlated with a high risk of recurrence and metastasis and advanced TNM stage in HCC patients. Functionally, loss- and gain-of-function studies showed that KIAA1199 promoted the migration, invasion, and metastasis of sorafenib-resistant HCC cells. Mechanistically, KIAA1199 is required for EGF-induced epithelial-mesenchymal transition (EMT) in sorafenib-resistant HCC cells by aiding in EGFR phosphorylation. In summary, our data uncover KIAA1199 as a novel sorafenib-tolerant promoting gene that plays an indispensable role in maintaining sorafenib-resistant HCC cell metastasis.
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