| Literature DB >> 31334575 |
Yanying Wang1, Pingping Zhu1, Jianjun Luo2, Jing Wang1,3, Zhiwei Liu4, Wei Wu2, Ying Du1, Buqing Ye1, Dongpeng Wang2,3, Lei He4, Weizheng Ren4, Jianyi Wang1,3, Xianhui Sun2,3, Runsheng Chen2, Yong Tian2,3, Zusen Fan1,3.
Abstract
Hepatocellular carcinoma (HCC) is the most prevalent liver cancer, characterized by a high rate of recurrence and heterogeneity. Liver cancer stem cells (CSCs) may well contribute to both of these pathological properties, but the mechanism underlying their self-renewal maintenance is poorly understood. Here, we identified a long noncoding RNA (lncRNA) termed HAND2-AS1 that is highly expressed in liver CSCs. Human HAND2-AS1 and its mouse ortholog lncHand2 display a high level of conservation. HAND2-AS1 is required for the self-renewal maintenance of liver CSCs to initiate HCC development. Mechanistically, HAND2-AS1 recruits the INO80 chromatin-remodeling complex to the promoter of BMPR1A, thereby inducing its expression and leading to the activation of BMP signaling. Importantly, interfering with expression of HAND2-AS1 by antisense oligonucleotides (ASOs) and BMPR1A by siRNAs has synergistic anti-tumorigenic effects on humanized HCC models. Moreover, knockout of lncHand2 or Bmpr1a in mouse hepatocytes impairs BMP signaling and suppresses the initiation of liver cancer. Our findings reveal that HAND2-AS1 promotes the self-renewal of liver CSCs and drives liver oncogenesis, offering a potential new target for HCC therapy.Entities:
Keywords: zzm321990HAND2-AS1zzm321990; BMP signaling; INO80 complex; cancer stem cells; hepatocellular carcinoma
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Year: 2019 PMID: 31334575 PMCID: PMC6717889 DOI: 10.15252/embj.2018101110
Source DB: PubMed Journal: EMBO J ISSN: 0261-4189 Impact factor: 11.598