Kernel-based hierarchical structural component models for pathway analysis on survival phenotype.

IF 1.7 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Genes & genomics Pub Date : 2024-12-01 Epub Date: 2024-09-26 DOI:10.1007/s13258-024-01569-9
Suhyun Hwangbo, Sungyoung Lee, Md Mozaffar Hosain, Taewan Goo, Seungyeoun Lee, Inyoung Kim, Taesung Park
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Abstract

Background: High-throughput sequencing, particularly RNA-sequencing (RNA-seq), has advanced differential gene expression analysis, revealing pathways involved in various biological conditions. Traditional pathway-based methods generally consider pathways independently, overlooking the correlations among them and ignoring quite a few overlapping biomarkers between pathways. In addition, most pathway-based approaches assume that biomarkers have linear effects on the phenotype of interest.

Objective: This study aims to develop the HisCoM-KernelS model to identify survival phenotype-related pathways by accommodating complex, nonlinear relationships between genes and survival outcomes, while accounting for inter-pathway correlations.

Methods: We applied HisCoM-KernelS model to the TCGA pancreatic ductal adenocarcinoma (PDAC) RNA-seq dataset, comprising 4,498 protein-coding genes mapped to 186 KEGG pathways from 148 PDAC samples. Kernel machine regression was used to model pathway effects on survival outcomes, incorporating hierarchical gene-pathway structures. Model parameters were estimated using the alternating least squares algorithm, and the significance of pathways was assessed through a permutation test.

Results: HisCoM-KernelS identified several pathways significantly associated with pancreatic cancer survival, including those corroborated by previous studies. HisCoM-KernelS, especially with the Gaussian kernel, showed a better balance of detection rate and number of significant pathways compared to four other existing pathway-based methods: HisCoM-PAGE, Global Test, GSEA, and CoxKM.

Conclusion: HisCoM-KernelS successfully extends pathway-based analysis to survival outcomes, capturing complex nonlinear gene effects and inter-pathway correlations. Its application to the TCGA PDAC dataset emphasizes its utility in identifying biologically relevant pathways, offering a robust tool for survival phenotype research in high-throughput sequencing data.

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基于核的分层结构组件模型用于生存表型的通路分析
背景:高通量测序,尤其是 RNA 测序(RNA-seq),推动了差异基因表达分析的发展,揭示了涉及各种生物条件的通路。传统的基于通路的方法通常独立考虑通路,忽略了通路之间的相关性,也忽略了通路之间大量重叠的生物标记物。此外,大多数基于通路的方法都假定生物标记物对相关表型具有线性影响:本研究旨在开发 HisCoM-KernelS 模型,通过考虑基因与生存结果之间复杂的非线性关系,同时考虑通路间的相关性,来识别与生存表型相关的通路:我们将 HisCoM-KernelS 模型应用于 TCGA 胰腺导管腺癌(PDAC)RNA-seq 数据集,该数据集由来自 148 个 PDAC 样本、映射到 186 个 KEGG 通路的 4498 个蛋白编码基因组成。利用核机器回归建立了通路对生存结果影响的模型,并纳入了分层基因通路结构。使用交替最小二乘法估计模型参数,并通过置换检验评估通路的显著性:结果:HisCoM-KernelS发现了几条与胰腺癌生存显著相关的通路,其中包括那些已被先前研究证实的通路。与其他四种基于通路的方法(HisCoM-PAGE、Global Test、GSEA 和 CoxKM)相比,HisCoM-KernelS(尤其是高斯核)在检测率和重要通路数量方面表现出更好的平衡:结论:HisCoM-KernelS 成功地将基于通路的分析扩展到了生存结果,捕捉到了复杂的非线性基因效应和通路间的相关性。它在 TCGA PDAC 数据集上的应用强调了它在识别生物相关通路方面的实用性,为高通量测序数据中的生存表型研究提供了一个强大的工具。
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来源期刊
Genes & genomics
Genes & genomics 生物-生化与分子生物学
CiteScore
3.70
自引率
4.80%
发文量
131
审稿时长
6-12 weeks
期刊介绍: Genes & Genomics is an official journal of the Korean Genetics Society (http://kgenetics.or.kr/). Although it is an official publication of the Genetics Society of Korea, membership of the Society is not required for contributors. It is a peer-reviewed international journal publishing print (ISSN 1976-9571) and online version (E-ISSN 2092-9293). It covers all disciplines of genetics and genomics from prokaryotes to eukaryotes from fundamental heredity to molecular aspects. The articles can be reviews, research articles, and short communications.
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