SRPS:多中心蛋白质组学亚型和生物标志物发现的生存强化迁移学习。

Linhai Xie, Pei Jiang, Cheng Chang
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引用次数: 0

摘要

在大规模和多中心队列研究中基于组学的分子分型是蛋白质组学驱动的精准医学(PDPM)的先决条件。然而,由于生物学异质性和技术不一致性,在不同队列中保持具有强大分子特征和与预后显著关联的亚型具有挑战性。在此,我们提出了一种称为生存强化患者分层(SRPS)的亚型算法,通过同时保留每种亚型的不同预后和分子特征,将已知亚型从发现队列调整到另一个队列。SRPS已经在模拟和现实世界的数据集上进行了基准测试,在这些数据集上,它显示出12%的分类准确率提高,并具有最佳的预测辨别能力。此外,根据计算的亚型显著性评分,一种“不受欢迎”的蛋白——肽基脯氨酸异构酶C (PPIC)被确定为对预后最差的肝细胞癌(HCC)患者进行亚型分型的前1显著蛋白。最终,实验证明PPIC在HCC中是一种促癌蛋白,证实了我们的工作是PDPM研究中可解释性机器学习引导生物学发现的示范。SRPS可在https://github.com/PHOENIXcenter/SRPS和https://ngdc.cncb.ac.cn/biocode/tool/BT007770公开获取。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
SRPS: Survival Reinforced Transfer Learning for Multicentric Proteomic Subtyping and Biomarker Discovery.

Omics-based molecular subtyping in large-scale and multicentric cohort studies is a prerequisite for proteomics-driven precision medicine (PDPM). However, keeping the subtypes with robust molecular features and significant associations with prognosis across different cohorts is challenging due to the biological heterogeneity and technical inconsistency. Herein, we propose a subtyping algorithm, named Survival Reinforced Patient Stratification (SRPS), to adapt the known subtypes from a discovery cohort to another by simultaneously preserving the distinct prognosis and molecular characteristics of each subtype. SRPS has been benchmarked on simulated and real-world datasets, where it shows a 12% increase in classification accuracy and possesses the best prognostic discrimination. Moreover, based on the calculated subtype significance score, an "unpopular" protein, Peptidylprolyl Isomerase C (PPIC), was identified as the top-1 remarkable protein for subtyping the hepatocellular carcinoma (HCC) patients with the worst prognosis. Eventually, PPIC was experimentally proved to be a pro-cancer protein in HCC, confirming our work as a demonstration of interpretable machine learning guided biological discovery in PDPM research. SRPS is publicly available at https://github.com/PHOENIXcenter/SRPS and https://ngdc.cncb.ac.cn/biocode/tool/BT007770.

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