根据基因表达的相互关系挖掘与胰腺导管腺癌相关的基因标记。

IF 1.9 4区 生物学 Q4 CELL BIOLOGY IET Systems Biology Pub Date : 2024-03-26 DOI:10.1049/syb2.12090
Zhao-Yue Zhang, Zi-Jie Sun, Dong Gao, Yu-Duo Hao, Hao Lin, Fen Liu
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引用次数: 0

摘要

胰腺导管腺癌(PDAC)占所有胰腺癌病例的 95%,给诊断和治疗带来了严峻挑战。及时诊断是提高患者生存率的关键,因此需要发现精确的生物标志物。我们引入了一种创新方法来识别基因标志物,以精确检测 PDAC。我们方法的核心思想是发现在 PDAC 和正常样本之间显示一致的相反相对表达和差异共表达模式的基因对。通过反转基因对分析和差异部分相关性分析来确定反转差异部分相关性(RDC)基因对。作者利用增量特征选择,完善了所选基因集,并构建了一个用于识别 PDAC 的机器学习模型。结果,该方法识别出了 10 个 RDC 基因对。在交叉验证过程中,该模型的准确率高达 96.1%,超过了基于基因表达的模型。独立验证数据实验证实了该模型的性能。富集分析揭示了这些基因参与了重要的生物学过程,并揭示了它们在 PDAC 发病机制中的潜在作用。总之,研究结果凸显了这10对RDC基因作为早期PDAC检测的有效诊断标记物的潜力,为改善患者预后和生存带来了希望。
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Excavation of gene markers associated with pancreatic ductal adenocarcinoma based on interrelationships of gene expression.

Pancreatic ductal adenocarcinoma (PDAC) accounts for 95% of all pancreatic cancer cases, posing grave challenges to its diagnosis and treatment. Timely diagnosis is pivotal for improving patient survival, necessitating the discovery of precise biomarkers. An innovative approach was introduced to identify gene markers for precision PDAC detection. The core idea of our method is to discover gene pairs that display consistent opposite relative expression and differential co-expression patterns between PDAC and normal samples. Reversal gene pair analysis and differential partial correlation analysis were performed to determine reversal differential partial correlation (RDC) gene pairs. Using incremental feature selection, the authors refined the selected gene set and constructed a machine-learning model for PDAC recognition. As a result, the approach identified 10 RDC gene pairs. And the model could achieve a remarkable accuracy of 96.1% during cross-validation, surpassing gene expression-based models. The experiment on independent validation data confirmed the model's performance. Enrichment analysis revealed the involvement of these genes in essential biological processes and shed light on their potential roles in PDAC pathogenesis. Overall, the findings highlight the potential of these 10 RDC gene pairs as effective diagnostic markers for early PDAC detection, bringing hope for improving patient prognosis and survival.

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来源期刊
IET Systems Biology
IET Systems Biology 生物-数学与计算生物学
CiteScore
4.20
自引率
4.30%
发文量
17
审稿时长
>12 weeks
期刊介绍: IET Systems Biology covers intra- and inter-cellular dynamics, using systems- and signal-oriented approaches. Papers that analyse genomic data in order to identify variables and basic relationships between them are considered if the results provide a basis for mathematical modelling and simulation of cellular dynamics. Manuscripts on molecular and cell biological studies are encouraged if the aim is a systems approach to dynamic interactions within and between cells. The scope includes the following topics: Genomics, transcriptomics, proteomics, metabolomics, cells, tissue and the physiome; molecular and cellular interaction, gene, cell and protein function; networks and pathways; metabolism and cell signalling; dynamics, regulation and control; systems, signals, and information; experimental data analysis; mathematical modelling, simulation and theoretical analysis; biological modelling, simulation, prediction and control; methodologies, databases, tools and algorithms for modelling and simulation; modelling, analysis and control of biological networks; synthetic biology and bioengineering based on systems biology.
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