Luo Jing, Wang Peng, Wang Ronghua, Wang Jinlin, Liu Man, Xiong Si, Li Yawen, Cheng Bin
Department of Gastroenterology and Hepatology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, P.R. China.
Department of Emergency, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, P.R. China.
Oncotarget. 2016 Feb 23;7(8):9525-37. doi: 10.18632/oncotarget.6672.
CD90 has been identified as a marker for liver cancer stem cells (CSCs) that are responsible for tumorigenic activity, but it is not known how CD90+ cells contribute to tumor initiation and progression. Our data demonstrated that high expression of CD90 in Hepatocellular Carcinoma (HCC) tissues correlated with venous filtration in HCC patients. CD90+ cells isolated from HCC cell lines exhibited increased tumorigenicity, chemoresistance, tumor invasion and metastasis. Notch pathway was activated in CD90+ cells and we found that inhibition of Notch pathway in CD90+ CSCs decreased tumorigenicity, cell invasion, migration and expression of stem cell related genes. Activation of Notch pathway in CD90- cells induced self-renewal, invasion and migration. Furthermore, we observed that cancer stem cell features were facilitated by stimulating G1-S transition in the cell cycle phase and inhibiting apoptosis mediated by Notch pathway. Our findings suggested CD90 could be used as a potential biomarker for HCC CSCs, and that cancer stem cell activity was elevated through up activated Notch pathway in CD90+ CSCs.
CD90已被确定为具有致瘤活性的肝癌干细胞(CSCs)的标志物,但尚不清楚CD90 +细胞如何促进肿瘤的起始和进展。我们的数据表明,肝癌(HCC)组织中CD90的高表达与HCC患者的静脉滤过相关。从HCC细胞系中分离出的CD90 +细胞表现出更高的致瘤性、化学抗性、肿瘤侵袭和转移能力。Notch通路在CD90 +细胞中被激活,我们发现抑制CD90 + CSCs中的Notch通路可降低致瘤性、细胞侵袭、迁移以及干细胞相关基因的表达。在CD90 -细胞中激活Notch通路可诱导自我更新、侵袭和迁移。此外,我们观察到,通过刺激细胞周期阶段中的G1 - S转变并抑制Notch通路介导的细胞凋亡,促进了癌症干细胞特征。我们的研究结果表明,CD90可作为HCC CSCs的潜在生物标志物,并且通过上调激活CD90 + CSCs中的Notch通路提高了癌症干细胞活性。