Exploring VEGF-Linked Pathways: Investigating Multiple miRNAs for Their Therapeutic Potential in Angiogenesis Targets and as Biomarkers in Recurrent Glioblastoma Multiforme.

IF 1.5 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Morteza Hadizadeh, Ramin Soltani, Taimour Langaee, Marziye Shadpirouz, Sorayya Ghasemi
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引用次数: 0

Abstract

Alternative pathways frequently operate as the origins of resistance to drugs that block the vascular endothelial growth factor (VEGF) pathway. To find possible therapeutic targets and indicators, this study explored the VEGF pathway and how miRNAs control it in recurrent glioblastoma multiforme (rGBM). Differentially expressed miRNAs (DEmiRNAs) were identified by using GBM GSE profiles (GSE32466). To find pathways containing DEmiRNAs, VEGF pathway genes, and their related genes, DIANA-miRPath v3.0 and the ToppGene database were utilized. miRNAs linked to VEGF signaling pathway genes, interactional genes, and DEmiRNAs were discovered by extracting common pathways. The ability of these miRNAs to distinguish rGBM patients from those with primary GBM was assessed using ROC analysis. The study revealed that in rGBM, 30 miRNAs were significantly up-regulated and 49 miRNAs were considerably down-regulated. Among them, the VEGF pathway was connected to 22 up-regulated miRNAs and 29 down-regulated miRNAs. The MAPK pathway shared the most genes with the VEGF pathway, accounting for 1,014 of the interacting genes, which were discovered to have interactions with VEGF signaling pathway genes. Furthermore, 14 miRNAs were identified as having a great deal of potential as molecular biomarkers and therapeutic targets for rGBM. The results indicate that the VEGF pathway in rGBM is regulated by a number of interrelated pathways. The discovered miRNAs hold promise as rGBM biomarkers and therapeutic targets, offering possibilities for novel therapy strategies and aiding rGBM diagnosis and prognosis.

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探索VEGF相关通路:研究多种miRNA在血管生成靶点中的治疗潜力以及作为复发性多型胶质母细胞瘤的生物标志物。
替代途径通常是阻断血管内皮生长因子(VEGF)途径的药物耐药性的来源。为了寻找可能的治疗靶点和指标,本研究探讨了复发性多形性胶质母细胞瘤(rGBM)中VEGF通路以及miRNA如何控制它。通过使用GBM GSE图谱(GSE32466)鉴定差异表达的miRNA(DEmiRNA)。为了找到包含DEmiRNA、VEGF通路基因及其相关基因的通路,利用DIANA-miRPathv3.0和ToppGene数据库。通过提取常见途径发现了与VEGF信号通路基因、相互作用基因和DEmiRNA相关的miRNA。使用ROC分析评估这些miRNA区分rGBM患者和原发性GBM患者的能力。研究表明,在rGBM中,30个miRNA显著上调,49个miRNA明显下调。其中,VEGF通路与22个上调的miRNA和29个下调的miRNA相连。MAPK通路与VEGF通路共享最多的基因,占1014个相互作用基因,这些基因被发现与VEGF信号通路基因有相互作用。此外,14种miRNA被鉴定为具有作为rGBM的分子生物标志物和治疗靶点的巨大潜力。结果表明,rGBM中的VEGF通路受到许多相关通路的调节。所发现的miRNA有望成为rGBM的生物标志物和治疗靶点,为新的治疗策略提供可能性,并帮助rGBM诊断和预后。
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来源期刊
CiteScore
3.60
自引率
0.00%
发文量
0
期刊介绍: The International Journal of Molecular and Cellular Medicine (IJMCM) is a peer-reviewed, quarterly publication of Cellular and Molecular Biology Research Center (CMBRC), Babol University of Medical Sciences, Babol, Iran. The journal covers all cellular & molecular biology and medicine disciplines such as the genetic basis of disease, biomarker discovery in diagnosis and treatment, genomics and proteomics, bioinformatics, computer applications in human biology, stem cells and tissue engineering, medical biotechnology, nanomedicine, cellular processes related to growth, death and survival, clinical biochemistry, molecular & cellular immunology, molecular and cellular aspects of infectious disease and cancer research. IJMCM is a free access journal. All open access articles published in IJMCM are distributed under the terms of the Creative Commons Attribution CC BY. The journal doesn''t have any submission and article processing charges (APCs).
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