LncRNA HHIP- as1通过稳定HHIP mRNA抑制肺鳞癌。

Zheyu Hu, Yixian Liu, Jin Tang, Renru Luo, Jiajia Qin, Zexun Mo, Jianjiang Xie, Xuan Jiang, Shuquan Wei, Chuwen Lin
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摘要

AIMSLung鳞状细胞癌(LUSC)每年导致40多万人死亡,但缺乏靶向治疗。HHIP (Hedgehog interaction Protein)是Hedgehog通路的主要拮抗剂,在LUSC中起重要作用;然而,监管机制仍不清楚。长链非编码RNA HHIP-AS1在不同的癌症中发挥抑制或促进作用,但其在LUSC中的作用尚不清楚。本文旨在探讨HHIP的调控机制以及HHIP- as1在LUSC中的作用。主要方法利用人LUSC的精确肺切片(PCLS)模拟LUSC的生长。通过慢病毒感染,在多种LUSC细胞系和PCLS中实现过表达和敲低。通过rna测序、免疫染色和CCK8检测等方法评估转录组谱和肺癌活性。主要发现:在LUSC中,HHIP独立于Hh通路调节。此外,HHIP-AS1的下调与预后不良有关。一致地,HHIP-AS1通过抑制细胞增殖和迁移来抑制LUSC生长。HHIP- as1敲低(KD)细胞的转录组分析揭示了HHIP下调。有趣的是,HHIP- as1 KD细胞和HHIP- KD细胞的转录组比较显示出高度的相似性。随后证实HHIP- as1在LUSC细胞中调控HHIP。值得注意的是,HHIP- as1对LUSC生长的调节是通过稳定HHIP mRNA实现的,而不是通过调节MIR-153-3P/PCDHGA9或MIR-425-5P/DNYC1I2实现的。最后,在来自人LUSC样本的PCLS中证实,HHIP- as1通过调节HHIP mRNA抑制LUSC。本研究揭示了HHIP-AS1在LUSC中作为一种新的肿瘤抑制因子,为LUSC的分子调控提供了新的见解,有助于开发新的治疗策略。
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LncRNA HHIP-AS1 suppresses lung squamous cell carcinoma by stabilizing HHIP mRNA.
AIMS Lung squamous cell carcinoma (LUSC) causes over 400,000 deaths annually, yet it lacks targeted therapy. A major antagonist of Hedgehog pathway, HHIP (Hedgehog Interacting Protein) plays an important role in LUSC; however, the regulatory mechanism remains unclear. Long non-coding RNA HHIP-AS1 plays suppressive or promotive roles in different cancers, but its role in LUSC remains unknown. This manuscript is to investigate regulatory mechanism of HHIP and the role of HHIP-AS1 in LUSC. MAIN METHODS Precision-cut lung slices (PCLS) from human LUSC samples are cultured to mimic LUSC growth. Overexpression and knockdown in multiple LUSC cell lines and PCLS are achieved by lentivirus infection. Transcriptome profile and lung cancer activity are evaluated by RNA-sequencing, immunostaining and CCK8 assay etc. KEY FINDINGS: HHIP is regulated independently of Hh pathway in LUSC. Additionally, downregulation of HHIP-AS1 is associated with poor prognosis. Consistently, HHIP-AS1 inhibits LUSC growth by suppressing cell proliferation and migration. Transcriptome profiling of HHIP-AS1 knockdown (KD) cells uncovered HHIP downregulation. Interestingly, a comparison between the transcriptomes of HHIP-AS1 KD or HHIP KD cells manifested high similarity. Subsequently it's confirmed that HHIP-AS1 regulates HHIP in LUSC cells. Notably, HHIP-AS1 regulation on LUSC growth is achieved through stabilizing HHIP mRNA rather than regulating MIR-153-3P/PCDHGA9 or MIR-425-5P/DNYC1I2. Finally, it's confirmed in PCLS from human LUSC samples that HHIP-AS1 suppresses LUSC via regulating HHIP mRNA. SIGNIFICANCE This study uncovers HHIP-AS1 as a novel tumor suppressor in LUSC and provides new insights into the molecular regulation of LUSC, which will help developing new therapeutic strategies.
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