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长链非编码 RNA HAND2-AS1 通过 BMP 信号促进肝癌干细胞自我更新。

LncRNA HAND2-AS1 promotes liver cancer stem cell self-renewal via BMP signaling.

机构信息

CAS Key Laboratory of Infection and Immunity, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing, China.

CAS Key Laboratory of RNA Biology, Institute of Biophysics, Chinese Academy of Sciences, Beijing, China.

出版信息

EMBO J. 2019 Sep 2;38(17):e101110. doi: 10.15252/embj.2018101110. Epub 2019 Jul 23.

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.

摘要

肝细胞癌(HCC)是最常见的肝癌,其特点是复发率高和异质性强。肝癌干细胞(CSCs)可能是这两种病理特性的主要原因,但它们自我更新维持的机制尚不清楚。在这里,我们鉴定了一种长非编码 RNA(lncRNA),称为 HAND2-AS1,它在肝 CSCs 中高度表达。人 HAND2-AS1 和其小鼠同源物 lncHand2 显示出高度的保守性。HAND2-AS1 是肝 CSCs 自我更新维持以启动 HCC 发展所必需的。在机制上,HAND2-AS1 招募 INO80 染色质重塑复合物到 BMPR1A 的启动子,从而诱导其表达并导致 BMP 信号的激活。重要的是,通过反义寡核苷酸(ASO)干扰 HAND2-AS1 的表达和通过 siRNA 干扰 BMPR1A 的表达对人源 HCC 模型具有协同的抗肿瘤作用。此外,在小鼠肝细胞中敲除 lncHand2 或 Bmpr1a 会抑制 BMP 信号并抑制肝癌的发生。我们的研究结果表明,HAND2-AS1 促进了肝 CSCs 的自我更新,并驱动了肝肿瘤的发生,为 HCC 治疗提供了一个新的潜在靶点。

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