Exploring the microRNA-mRNA regulatory network associated with solasonine in bladder cancer.

IF 1.7 3区 医学 Q4 ANDROLOGY Translational andrology and urology Pub Date : 2024-05-31 Epub Date: 2024-05-27 DOI:10.21037/tau-23-469
Kun Fang, Da-Lang Fang, Hui Yu, Yu-Ang Chen, Pei-Ze Yu, Zi-Fan Wang, Rui-Bin Zhang, Wen Yang, Lei Tao, Hiroshi Fukushima, Yang Dong, Cong-Hui Han
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Abstract

Background: Solasonine has been demonstrated to exert an inhibitory effect on bladder cancer (BC), but the potential mechanisms remain unclear. Therefore, the aim of this study is to explore the association between microRNAs (miRNAs)-mediated regulation and the anti-tumor activities of solasonine in BC.

Methods: MiRNA sequencing was performed to identify the differentially expressed microRNAs (DE-miRNAs) associated with solasonine in BC cells. Functional enrichment analyses of the DE-miRNAs activated and inhibited by solasonine were then conducted. The DE-miRNAs with prognostic value for BC and those differentially expressed in the BC samples were subsequently identified as the hub DE-miRNAs. After identifying the messenger RNAs (mRNAs) that were targeted by the hub DE-miRNAs and those differentially expressed in the BC samples, a protein-protein interaction analysis was performed to identify the core downstream genes, which were then used to construct a solasonine-miRNA-mRNA regulatory network.

Results: A total of 27 activated and 19 inhibited solasonine-mediated DE-miRNAs were identified that were found to be associated with several tumor-related biological functions and pathways. After integrating the results of the survival analysis and expression assessment, the following nine hub DE-miRNAs were identified: hsa-miR-127-3p, hsa-miR-450b-5p, hsa-miR-99a-5p, hsa-miR-197-3p, hsa-miR-423-3p, hsa-miR-4326, hsa-miR-625-3p, hsa-miR-625-5p, and hsa-miR-92a-3p. The DE-mRNAs targeted by the hub DE-miRNAs were predicted, and 30 core downstream genes were used to construct the solasonine-miRNA-mRNA regulatory network. miR-450b-5p was shown to be associated with the most mRNAs in this network, which suggests that it plays a crucial role in the solasonine-mediated anti-BC effect.

Conclusions: A regulatory network, including solasonine, miRNAs, and mRNAs related to BC, was constructed. This network provides extensive insights into the molecular regulatory mechanisms that underlie the anti-cancer efficacy of solasonine in BC.

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探索膀胱癌中与索拉宁相关的微RNA-mRNA调控网络
背景:已证实索拉宁对膀胱癌(BC)有抑制作用,但其潜在机制仍不清楚。因此,本研究旨在探讨微RNAs(miRNAs)介导的调控与索拉宁在膀胱癌中的抗肿瘤活性之间的关联:方法:对 BC 细胞进行 MiRNA 测序,以确定与 Solasonine 相关的差异表达 microRNAs(DE-miRNAs)。然后对被索拉宁激活和抑制的 DE-miRNA 进行了功能富集分析。随后,对 BC 有预后价值的 DE-miRNA 和在 BC 样本中差异表达的 DE-miRNA 被确定为中枢 DE-miRNA。在确定了枢纽DE-miRNAs靶向的信使RNAs(mRNAs)以及在BC样本中差异表达的信使RNAs之后,进行了蛋白-蛋白相互作用分析,以确定核心下游基因,然后利用这些基因构建了一个溶血-miRNA-mRNA调控网络:结果:共鉴定出27个激活的和19个抑制的溶血素介导的DE-miRNA,发现这些DE-miRNA与多种肿瘤相关的生物学功能和通路有关。综合生存分析和表达评估的结果,确定了以下九个枢纽 DE-miRNA:hsa-miR-127-3p、hsa-miR-450b-5p、hsa-miR-99a-5p、hsa-miR-197-3p、hsa-miR-423-3p、hsa-miR-4326、hsa-miR-625-3p、hsa-miR-625-5p 和 hsa-miR-92a-3p。结果表明,miR-450b-5p与该网络中最多的mRNA相关,这表明它在溶菌素介导的抗白血病效应中发挥了关键作用:结论:研究人员构建了一个包括索拉宁、miRNA和与BC相关的mRNA的调控网络。结论:该研究构建了一个包括索拉宁、miRNAs和与BC相关的mRNAs的调控网络,为了解索拉宁在BC中的抗癌作用的分子调控机制提供了广泛的视角。
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来源期刊
CiteScore
4.10
自引率
5.00%
发文量
80
期刊介绍: ranslational Andrology and Urology (Print ISSN 2223-4683; Online ISSN 2223-4691; Transl Androl Urol; TAU) is an open access, peer-reviewed, bi-monthly journal (quarterly published from Mar.2012 - Dec. 2014). The main focus of the journal is to describe new findings in the field of translational research of Andrology and Urology, provides current and practical information on basic research and clinical investigations of Andrology and Urology. Specific areas of interest include, but not limited to, molecular study, pathology, biology and technical advances related to andrology and urology. Topics cover range from evaluation, prevention, diagnosis, therapy, prognosis, rehabilitation and future challenges to urology and andrology. Contributions pertinent to urology and andrology are also included from related fields such as public health, basic sciences, education, sociology, and nursing.
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