Hu Zheyu, Liu Yixian, Tang Jin, Luo Renru, Qin Jiajia, Mo Zexun, Xie Jianjiang, Jiang Xuan, Wei Shuquan, Lin Chuwen
Department of histology and embryology, School of Medicine, Shenzhen Campus of Sun Yat-sen University, Sun Yat-sen University, 66 Gongchang Road, Shenzhen 518107, China.
Department of Pulmonary and Critical Care Medicine, Guangzhou First People's Hospital, School of Medicine, South China University of Technology, 1 Panfu Road, Guangzhou 510180, China.
Life Sci. 2023 May 15;321:121578. doi: 10.1016/j.lfs.2023.121578. Epub 2023 Mar 21.
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.
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.
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.
肺鳞状细胞癌(LUSC)每年导致超过40万例死亡,但缺乏靶向治疗。Hedgehog信号通路的主要拮抗剂HHIP(Hedgehog相互作用蛋白)在LUSC中起重要作用;然而,其调控机制仍不清楚。长链非编码RNA HHIP-AS1在不同癌症中发挥抑制或促进作用,但其在LUSC中的作用尚不清楚。本研究旨在探讨HHIP的调控机制以及HHIP-AS1在LUSC中的作用。
培养来自人LUSC样本的精密肺切片(PCLS)以模拟LUSC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测定等评估转录组图谱和肺癌活性。
在LUSC中,HHIP的调控独立于Hh信号通路。此外,HHIP-AS1的下调与预后不良相关。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)细胞的转录组分析发现HHIP下调。有趣的是,HHIP-AS1 KD或HHIP KD细胞的转录组之间的比较显示出高度相似性。随后证实HHIP-AS1在LUSC细胞中调节HHIP。值得注意的是,HHIP-AS1对LUSC生长的调节是通过稳定HHIP mRNA而不是调节MIR-153-3P/PCDHGA9或MIR-425-5P/DNYC1I2来实现的。最后,在来自人LUSC样本的PCLS中证实,HHIP-AS1通过调节HHIP mRNA来抑制LUSC。
本研究发现HHIP-AS1是LUSC中的一种新型肿瘤抑制因子,并为LUSC的分子调控提供了新的见解,这将有助于开发新的治疗策略。