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环状 RNA circ_0004630 通过海绵吸附 microRNA-1208 和调节富含亮氨酸重复激酶 2 的表达促进非小细胞肺癌的恶性转化和糖酵解。

Circular RNA circ_0004630 promotes malignancy and glycolysis of nonsmall cell lung cancer by sponging microRNA-1208 and regulating leucine-rich repeat kinase 2 expression.

机构信息

Department of Respiratory Medicine, Shaanxi Provincial People's Hospital, Xi'an, China.

Clinical Laboratory, Shaanxi Provincial People's Hospital, Xi'an City, China.

出版信息

J Biochem Mol Toxicol. 2024 Dec;38(12):e23811. doi: 10.1002/jbt.23811.

Abstract

Emerging evidence has discovered that circular RNAs play important regulators of nonsmall cell lung cancer (NSCLC), but the role and potential molecular mechanism of hsa_circ_100549 (circ_0004630) involved in NSCLC is poorly defined. In this study, circ_0004630, microRNA-1208 (miR-1208), and leucine-rich repeat kinase 2 (LRRK2) expression were detected using real-time quantitative polymerase chain reaction. Cell proliferation, colony formation, apoptosis, and invasion were assessed using 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2-H-tetrazolium bromide (MTT), 5-ethynyl-2'-deoxyuridine, colony formation, flow cytometry, and transwell assays. Protein levels of glucose transporter 1, Hexokinase 2, and LRRK2 were detected using western blot assay. Glucose consumption, lactate production, and adenosine triphosphate content were assessed using the corresponding kits. After predicting via bioinformatics software Circinteractome and Targetscan, the binding between miR-1208 and circ_0004630 or LRRK2 was verified by a dual-luciferase reporter, RNA immunoprecipitation, and RNA pull-down assay. The xenograft tumor model analyzed the biological role circ_000460 on tumor growth in vivo. It was found that circ_0004630 and LRRK2 were increased, and miR-1208 was low expression in NSCLC tissues and cells. Functionally, the downregulation of circ_0004630 inhibited NSCLC cell proliferation, invasion, glycolysis, and accelerated apoptosis in vitro. In mechanism, circ_0004630 might work as a sponge of miR-1208 to modulate LRRK2 expression. In addition, DUXAP8 deficiency cured neuroblastoma tumor growth in vivo. In conclusion, circ_0004630 knockdown might suppress NSCLC cell proliferation, metastasis, and glycolysis partly by the miR-1208/LRRK2 axis. Our findings hinted at an important theoretical basis for further elucidating the pathogenesis of NSCLC and targeted therapy.

摘要

新兴证据表明,环状 RNA 作为非小细胞肺癌(NSCLC)的重要调控因子发挥作用,但 hsa_circ_100549(circ_0004630)在 NSCLC 中的作用和潜在分子机制尚不清楚。在这项研究中,使用实时定量聚合酶链反应检测 circ_0004630、微小 RNA-1208(miR-1208)和富含亮氨酸重复激酶 2(LRRK2)的表达。使用 3-(4,5-二甲基-2-噻唑基)-2,5-二苯基-2-H-四唑溴盐(MTT)、5-乙炔基-2'-脱氧尿苷、集落形成、流式细胞术和 Transwell 测定评估细胞增殖、集落形成、凋亡和侵袭。使用 Western blot 测定检测葡萄糖转运蛋白 1、己糖激酶 2 和 LRRK2 的蛋白水平。使用相应试剂盒评估葡萄糖消耗、乳酸生成和三磷酸腺苷含量。通过生物信息学软件 Circinteractome 和 Targetscan 预测后,通过双荧光素酶报告、RNA 免疫沉淀和 RNA 下拉测定验证 miR-1208 与 circ_0004630 或 LRRK2 的结合。分析体内 circ_000460 对肿瘤生长的生物学作用的异种移植肿瘤模型。结果发现,NSCLC 组织和细胞中 circ_0004630 和 LRRK2 升高,miR-1208 表达降低。功能上,circ_0004630 的下调抑制 NSCLC 细胞的增殖、侵袭、糖酵解并加速体外凋亡。在机制上,circ_0004630 可能作为 miR-1208 的海绵来调节 LRRK2 的表达。此外,DUXAP8 缺乏症可治愈体内神经母细胞瘤肿瘤的生长。总之,circ_0004630 的敲低可能部分通过 miR-1208/LRRK2 轴抑制 NSCLC 细胞的增殖、转移和糖酵解。我们的研究结果为进一步阐明 NSCLC 的发病机制和靶向治疗提供了重要的理论依据。

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