Identification of Molecular Mechanisms of Ameloblastoma and Drug Repositioning by Integration of Bioinformatics Analysis and Molecular Docking Simulation.

IF 2.3 Q3 BIOCHEMICAL RESEARCH METHODS
Bioinformatics and Biology Insights Pub Date : 2024-05-28 eCollection Date: 2024-01-01 DOI:10.1177/11779322241256459
Suthipong Chujan, Nutsira Vajeethaveesin, Jutamaad Satayavivad, Nakarin Kitkumthorn
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引用次数: 0

Abstract

Background: Ameloblastoma (AM) is a benign tumor locally originated from odontogenic epithelium that is commonly found in the jaw. This tumor makes aggressive invasions and has a high recurrence rate. This study aimed to investigate the differentially expressed genes (DEGs), biological function alterations, disease targets, and existing drugs for AM using bioinformatics analysis.

Methods: The data set of AM was retrieved from the GEO database (GSE132474) and identified the DEGs using bioinformatics analysis. The biological alteration analysis was applied to Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways. Protein-protein interaction (PPI) network analysis and hub gene identification were screened through NetworkAnalyst. The transcription factor-protein network was constructed via OmicsNet. We also identified candidate compounds from L1000CDS2 database. The target of AM and candidate compounds were verified using docking simulation.

Results: Totally, 611 DEGs were identified. The biological function enrichment analysis revealed glycosaminoglycan and GABA (γ-aminobutyric acid) signaling were most significantly up-regulated and down-regulated in AM, respectively. Subsequently, hub genes and transcription factors were screened via the network and showed FOS protein was found in both networks. Furthermore, we evaluated FOS protein to be a therapeutic target in AMs. Candidate compounds were screened and verified using docking simulation. Tanespimycin showed the greatest affinity binding value to bind FOS protein.

Conclusions: This study presented the underlying molecular mechanisms of disease pathogenesis, biological alteration, and important pathways of AMs and provided a candidate compound, Tanespimycin, targeting FOS protein for the treatment of AMs.

通过整合生物信息学分析和分子对接模拟,识别母细胞瘤的分子机制和药物重新定位。
背景:釉母细胞瘤(Ameloblastoma,AM)是一种良性肿瘤,局部来源于牙源性上皮,常见于颌骨。这种肿瘤侵袭性强,复发率高。本研究旨在通过生物信息学分析研究AM的差异表达基因(DEGs)、生物功能改变、疾病靶点和现有药物:方法:从 GEO 数据库(GSE132474)中检索 AM 数据集,并利用生物信息学分析鉴定 DEGs。生物改变分析应用于基因本体(GO)和京都基因组百科全书(KEGG)通路。通过 NetworkAnalyst 筛选了蛋白质-蛋白质相互作用(PPI)网络分析和枢纽基因鉴定。转录因子-蛋白质网络是通过 OmicsNet 构建的。我们还从 L1000CDS2 数据库中确定了候选化合物。通过对接模拟验证了 AM 的靶点和候选化合物:结果:共鉴定出 611 个 DEGs。生物功能富集分析表明,糖胺聚糖和 GABA(γ-氨基丁酸)信号传导在 AM 中分别显著上调和下调。随后,我们通过网络筛选了枢纽基因和转录因子,结果表明在两个网络中都发现了FOS蛋白。此外,我们还评估了FOS蛋白作为AM治疗靶点的可能性。通过对接模拟筛选并验证了候选化合物。Tanespimycin 与 FOS 蛋白的亲和力结合值最高:本研究揭示了AMs发病的分子机制、生物学改变和重要通路,并提供了一种以FOS蛋白为靶点的候选化合物--Tanespimycin,用于治疗AMs。
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来源期刊
Bioinformatics and Biology Insights
Bioinformatics and Biology Insights BIOCHEMICAL RESEARCH METHODS-
CiteScore
6.80
自引率
1.70%
发文量
36
审稿时长
8 weeks
期刊介绍: Bioinformatics and Biology Insights is an open access, peer-reviewed journal that considers articles on bioinformatics methods and their applications which must pertain to biological insights. All papers should be easily amenable to biologists and as such help bridge the gap between theories and applications.
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