LGR5型
干细胞
生物
癌症干细胞
地穴
条件基因敲除
细胞生物学
肠上皮
癌症研究
转录因子
癌变
癌症
Wnt信号通路
上皮
信号转导
遗传学
基因
表型
内分泌学
作者
Pingping Zhu,Jiayi Wu,Yanying Wang,Xiaoxiao Zhu,Tiankun Lu,Benyu Liu,Luyun He,Buqing Ye,Shuo Wang,Shu Meng,Dongdong Fan,Jing Wang,Liuliu Yang,Xiwen Qin,Ying Du,Chong Li,Lei He,Weizheng Ren,Xin Wu,Yong Tian,Zusen Fan
标识
DOI:10.1038/s41556-018-0194-0
摘要
The intestinal epithelium harbours remarkable self-renewal capacity that is driven by Lgr5+ intestinal stem cells (ISCs) at the crypt base. However, the molecular mechanism controlling Lgr5+ ISC stemness is incompletely understood. We show that a Gata6 long noncoding RNA (lncGata6) is highly expressed in ISCs. LncGata6 knockout or conditional knockout in ISCs impairs the stemness of ISCs and epithelial regeneration. Mechanistically, lncGata6 recruits the NURF complex onto the Ehf promoter to induce its transcription, which promotes the expression of Lgr4/5 to enhance Wnt signalling activation. Moreover, the human orthologue lncGATA6 is highly expressed in the cancer stem cells of colorectal cancer and promotes tumour initiation and progression. Antisense oligonucleotides against lncGATA6 exhibit strong therapeutic efficacy on colorectal cancer. Thus, targeting lncGATA6 will have potential clinical applications in colorectal cancer treatment as an ideal therapeutic target.
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