LGR5型
癌症干细胞
索拉非尼
癌症研究
肝癌
肝细胞癌
类有机物
干细胞
癌症
生物
癌细胞
免疫学
医学
内科学
细胞生物学
作者
Wanlu Cao,Meng Li,Jiaye Liu,Shaoshi Zhang,Lisanne Noordam,Monique M.A. Verstegen,Ling Wang,Buyun Ma,Shan Li,Wenshi Wang,Michiel Bolkestein,Michael Doukas,Kan Chen,Zhongren Ma,Marco J. Bruno,Dave Sprengers,Jaap Kwekkeboom,Luc J. W. van der Laan,Ron Smits,Maikel P. Peppelenbosch,Qiuwei Pan
标识
DOI:10.1038/s41467-020-15846-0
摘要
Cancer stem cells (CSCs) or tumor-initiating cells (TICs) are thought to be the main drivers for disease progression and treatment resistance across various cancer types. Identifying and targeting these rare cancer cells, however, remains challenging with respect to therapeutic benefit. Here, we report the enrichment of LGR5 expressing cells, a well-recognized stem cell marker, in mouse liver tumors, and the upregulation of LGR5 expression in human hepatocellular carcinoma. Isolated LGR5 expressing cells from mouse liver tumors are superior in initiating organoids and forming tumors upon engraftment, featuring candidate TICs. These cells are resistant to conventional treatment including sorafenib and 5-FU. Importantly, LGR5 lineage ablation significantly inhibits organoid initiation and tumor growth. The combination of LGR5 ablation with 5-FU, but not sorafenib, further augments the therapeutic efficacy in vivo. Thus, we have identified the LGR5+ compartment as an important TIC population, representing a viable therapeutic target for combating liver cancer.
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