miR-16-5p在调节肺癌症细胞ADP-核糖基化因子样肿瘤抑制基因1中的作用和拮抗作用。

Pub Date : 2023-10-01 DOI:10.5152/eurasianjmed.2023.23073
Tuğba Nurcan Yüksel, Esra Bozgeyik, İbrahim Bozgeyik
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引用次数: 0

摘要

目的:ADP-核糖基化因子样肿瘤抑制基因1是小鸟苷三磷酸酶Ras超家族的成员,已知其参与人类癌症多阶段发展的多种调节途径。此外,据报道,与对照相比,在癌症细胞系和肿瘤组织中,ADP-核糖基化因子样肿瘤抑制基因1的表达水平显著降低。因此,ADP-核糖基化因子样肿瘤抑制基因1基因的调节缺陷似乎在包括癌症在内的人类癌症的形成和发展中具有关键的肿瘤抑制作用。此外,调节ADP-核糖基化因子样肿瘤抑制基因1表达的微小RNA以前没有描述过。因此,本研究旨在揭示miR-16-5p对ADP-核糖基化因子样肿瘤抑制基因1基因调控的影响。材料与方法:采用A549肺腺癌细胞。对于miR-16-5p的过表达和沉默实验,分别使用合成的微小RNA模拟物和抑制剂。基因表达分析是在定量实时聚合酶链式反应的帮助下实现的。结果:MiR-16-5p被鉴定为ADP核糖基化因子样抑癌基因1的预测靶点,并通过过表达和沉默实验直接靶向ADP核糖基因子样抑瘤基因1的表达。具体而言,发现miR-16-5p过表达的A549细胞显示出ADP核糖基化因子样肿瘤抑制基因1基因表达的降低,而miR16-5p过表达细胞显示出表达的增加。这些发现可能表明miR-16-5p是转录后调节ADP核糖基化因子样肿瘤抑制基因1表达的直接调控微小RNA,它可能是该基因在癌症中下调的原因。
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The Role and Antagonistic Effects of miR-16-5p in the Regulation of ADP-Ribosylation Factor-Like Tumor Suppressor Gene 1 in Lung Cancer Cells.

Objective: ADP-ribosylation factor-like tumor suppressor gene 1 is a member of the Ras superfamily of small guanosine triphosphatases that are known to be involved in multiple regulatory pathways in the multistage development of human cancers. Also, ADP-ribosylation factor-like tumor suppressor gene 1 expression levels have been reported to be dramatically lower in both cancer cell lines and tumor tissues compared to controls. Accordingly, defects in the regulation of the ADP-ribosylation factor-like tumor suppressor gene 1 gene seems have key tumor suppressive effects in the formation and development of human cancers including lung cancer. Moreover, microRNAs regulating the expression of ADP-ribosylation factor-like tumor suppressor gene 1 have not been described previously. Accordingly, the present study aimed to reveal the influence of miR-16-5p on the regulation of ADP-ribosylation factor-like tumor suppressor gene 1 gene.

Materials and methods: A549 lung adenocarcinoma cells were used. For the overexpression and silencing experiments of miR-16-5p synthetic microRNA mimics and inhibitors were used, respectively. Gene expression analyses were achieved with the help of quantitative real-time polymerase chain reaction.

Results: MiR-16-5p was identified to be predictive target of ADP-ribosylation factor-like tumor suppressor gene 1 and directly targets the expression of ADP-ribosylation factor-like tumor suppressor gene 1 as revealed by the overexpression and silencing experiments. Specifically, it was found that miR-16-5p-overexpressed A549 cells showed a decrease in ADP-ribosylation factor-like tumor suppressor gene 1 gene expression, whereas miR16-5p-suppressed cells showed an increase in expression. These findings possibly suggest that miR-16-5p is the direct regulatory microRNA that posttranscriptionally regulates the expression of ADP-ribosylation factor-like tumor suppressor gene 1.

Conclusion: Collectively, miR-16-5p seems to be a key regulatory molecule involved in the posttranscriptional regulation of the ADP-ribosylation factor-like tumor suppressor gene 1, and it might be responsible for the downregulation of this gene in lung cancer.

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