Lung Adenocarcinoma Systems Biomarker and Drug Candidates Identified by Machine Learning, Gene Expression Data, and Integrative Bioinformatics Pipeline.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
ACS Applied Bio Materials Pub Date : 2024-08-01 Epub Date: 2024-07-09 DOI:10.1089/omi.2024.0121
Semra Melis Soyer, Pemra Ozbek, Ceyda Kasavi
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Abstract

Lung adenocarcinoma (LUAD) is a significant planetary health challenge with its high morbidity and mortality rate, not to mention the marked interindividual variability in treatment outcomes and side effects. There is an urgent need for robust systems biomarkers that can help with early cancer diagnosis, prediction of treatment outcomes, and design of precision/personalized medicines for LUAD. The present study aimed at systems biomarkers of LUAD and deployed integrative bioinformatics and machine learning tools to harness gene expression data. Predictive models were developed to stratify patients based on prognostic outcomes. Importantly, we report here several potential key genes, for example, PMEL and BRIP1, and pathways implicated in the progression and prognosis of LUAD that could potentially be targeted for precision/personalized medicine in the future. Our drug repurposing analysis and molecular docking simulations suggested eight drug candidates for LUAD such as heat shock protein 90 inhibitors, cardiac glycosides, an antipsychotic agent (trifluoperazine), and a calcium ionophore (ionomycin). In summary, this study identifies several promising leads on systems biomarkers and drug candidates for LUAD. The findings also attest to the importance of integrative bioinformatics, structural biology and machine learning techniques in biomarker discovery, and precision oncology research and development.

通过机器学习、基因表达数据和综合生物信息学管道确定肺腺癌系统生物标记物和候选药物。
肺腺癌(LUAD)的发病率和死亡率都很高,而且治疗效果和副作用在个体间存在明显差异,因此是地球健康面临的重大挑战。目前急需稳健的系统生物标志物,以帮助进行癌症早期诊断、预测治疗结果以及设计治疗 LUAD 的精准/个性化药物。本研究以 LUAD 的系统生物标志物为目标,采用综合生物信息学和机器学习工具来利用基因表达数据。我们建立了预测模型,根据预后结果对患者进行分层。重要的是,我们在此报告了几个潜在的关键基因,如PMEL和BRIP1,以及与LUAD的进展和预后有关的通路,这些基因和通路在未来有可能成为精准/个性化医疗的靶点。我们的药物再利用分析和分子对接模拟提出了八种治疗LUAD的候选药物,如热休克蛋白90抑制剂、强心甙、抗精神病药物(三氟哌嗪)和钙离子拮抗剂(离子霉素)。总之,这项研究发现了一些有希望的 LUAD 系统生物标记物和候选药物线索。研究结果还证明了综合生物信息学、结构生物学和机器学习技术在生物标志物发现和精准肿瘤学研发中的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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