Zhang Yajun, Shi Woda, Chen Rongjin, Gu Yan, Zhao Mengjie, Song Jianxiang, Shi Zhan, Wu Jixiang, Chang HuiWen, Liu Ming
Cardiothoracic Surgery, Affiliated Hospital sixth of Nantong University, The Yancheng School of Clinical Medicine of Nanjing Medical University, Yancheng Third People's Hospital, Yancheng, 224000, China.
Medical School of Nantong University, Nantong, 226007, China; Department of Cardiothoracic Surgery, Affiliated Hospital sixth of Nantong University, The Yancheng School of Clinical Medicine of Nanjing Medical University, Yancheng Third People's Hospital, Yancheng, 224000, China.
Transl Oncol. 2024 Jun;44:101931. doi: 10.1016/j.tranon.2024.101931. Epub 2024 Apr 10.
LncRNAs are vital regulators for lung squamous cell carcinoma (LUSC). However, the detailed role that LINC01133 plays in LUSC is unclear. This work sought to explore the potential function of LINC01133.Levels of LINC01133, miR-30d-5p, and MARCKS were separately tested in both tissues and cells using qRT-PCR. Proliferation was assessed through MTT experiment and apoptosis was detected upon flow cytometry. Transwell experiments were implemented to evaluate migratory and invasive abilities. The interaction between two genes was affirmed through luciferase reporter assay and RNA pull-down experiment. Western blotting measured the protein level of MARCKS. Animal models were established and tissues were taken for IHC analysis of MARCKS and Ki67.LINC01133 was elevated in LUSC and its downregulation could suppress proliferation, migration and invasion but induced apoptosis. LINC01133 interacted with and regulated the binding of miR-30d-5p to MARCKS. LINC01133/miR-30d-5p axis mediated proliferation, apoptosis, migration and invasion in LUSC cells, as well as modulated tumor growth in animal models. LINC01133 interacted with miR-30d-5p to modulate MARCKS expression, contributes to promoted cell proliferation, migration, invasion, and inhibited cell apoptosis in vitro, and promoted tumor growth in vivo. These findings could provide possible therapeutic targets in view of LUSC treatment in the future.
长链非编码RNA(lncRNAs)是肺鳞状细胞癌(LUSC)的重要调节因子。然而,LINC01133在LUSC中发挥的具体作用尚不清楚。本研究旨在探索LINC01133的潜在功能。采用qRT-PCR分别检测LINC01133、miR-30d-5p和MARCKS在组织和细胞中的水平。通过MTT实验评估细胞增殖情况,采用流式细胞术检测细胞凋亡。进行Transwell实验以评估细胞的迁移和侵袭能力。通过荧光素酶报告基因检测和RNA下拉实验确定两个基因之间的相互作用。蛋白质印迹法检测MARCKS的蛋白水平。建立动物模型并取组织进行MARCKS和Ki67的免疫组化分析。LINC01133在LUSC中表达升高,其下调可抑制细胞增殖、迁移和侵袭,但诱导细胞凋亡。LINC01133与miR-30d-5p相互作用并调节其与MARCKS的结合。LINC01133/miR-30d-5p轴介导LUSC细胞的增殖、凋亡、迁移和侵袭,并在动物模型中调节肿瘤生长。LINC01133与miR-30d-5p相互作用以调节MARCKS表达,有助于促进体外细胞增殖、迁移、侵袭并抑制细胞凋亡,以及促进体内肿瘤生长。这些发现可能为未来LUSC的治疗提供潜在的靶点。