Li Wei, Miao Shuanlin, Miao Manyuan, Li Renshuan, Cao Xiaopeng, Zhang Kun, Huang Genzuan, Fu Bin
a Department of Surgical Oncology , Xianyang Hospital of Yan'an University , Xianyang, Shannxi , China.
Cancer Invest. 2016 Oct 20;34(9):424-430. doi: 10.1080/07357907.2016.1227442. Epub 2016 Sep 22.
Previous studies have established that hedgehog (Hh) signaling mediates tumor-stroma interaction and promotes hepatocellular carcinoma progression. Here, we demonstrated that activation of Hh signaling in hepatic stellate cell (HSC) line LX-2 by Huh-7-derived sonic Hh led to increased secretion of angiogenic factors and promoted angiogenesis in vitro. The activated LX-2 also enhanced vascular mimicry of hepatoma cells. Furthermore, co-injection of Huh-7 and LX-2 significantly accelerated tumor growth with enhanced angiogenesis compared with Huh-7 alone, which could be partly abrogated by Hh signaling inhibitor. Collectively, our data showed that paracrine Hh signaling mediated pro-angiogenic function of HSC and enhanced hepatoma growth.
先前的研究已证实,刺猬蛋白(Hh)信号传导介导肿瘤-基质相互作用并促进肝细胞癌进展。在此,我们证明,源自Huh-7的音猬因子(sonic Hh)激活肝星状细胞(HSC)系LX-2中的Hh信号传导,导致血管生成因子分泌增加,并在体外促进血管生成。活化的LX-2还增强了肝癌细胞的血管拟态。此外,与单独注射Huh-7相比,联合注射Huh-7和LX-2可显著加速肿瘤生长并增强血管生成,而Hh信号传导抑制剂可部分消除这种作用。总体而言,我们的数据表明旁分泌Hh信号传导介导HSC的促血管生成功能并增强肝癌生长。