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深度学习将组织病理学和蛋白质基因组学整合到泛癌水平。

Deep learning integrates histopathology and proteogenomics at a pan-cancer level.

机构信息

Institute for Systems Genetics, NYU Grossman School of Medicine, New York, NY 10016, USA; Department of Biochemistry and Molecular Pharmacology, NYU Grossman School of Medicine, New York, NY 10016, USA.

Department of Pathology and Laboratory Medicine, Mount Sinai Hospital and Laboratory Medicine and Pathobiology, University of Toronto, Toronto M5G 1X5, ON, Canada.

出版信息

Cell Rep Med. 2023 Sep 19;4(9):101173. doi: 10.1016/j.xcrm.2023.101173. Epub 2023 Aug 14.

Abstract

We introduce a pioneering approach that integrates pathology imaging with transcriptomics and proteomics to identify predictive histology features associated with critical clinical outcomes in cancer. We utilize 2,755 H&E-stained histopathological slides from 657 patients across 6 cancer types from CPTAC. Our models effectively recapitulate distinctions readily made by human pathologists: tumor vs. normal (AUROC = 0.995) and tissue-of-origin (AUROC = 0.979). We further investigate predictive power on tasks not normally performed from H&E alone, including TP53 prediction and pathologic stage. Importantly, we describe predictive morphologies not previously utilized in a clinical setting. The incorporation of transcriptomics and proteomics identifies pathway-level signatures and cellular processes driving predictive histology features. Model generalizability and interpretability is confirmed using TCGA. We propose a classification system for these tasks, and suggest potential clinical applications for this integrated human and machine learning approach. A publicly available web-based platform implements these models.

摘要

我们介绍了一种开创性的方法,将病理学成像与转录组学和蛋白质组学相结合,以识别与癌症关键临床结局相关的预测性组织学特征。我们利用了来自 CPTAC 的 6 种癌症类型的 657 名患者的 2755 张 H&E 染色组织病理学幻灯片。我们的模型有效地再现了人类病理学家很容易做出的区分:肿瘤与正常组织(AUROC=0.995)和组织起源(AUROC=0.979)。我们进一步研究了在通常不单独使用 H&E 进行的任务上的预测能力,包括 TP53 预测和病理分期。重要的是,我们描述了以前在临床环境中未使用过的预测形态。转录组学和蛋白质组学的结合确定了驱动预测性组织学特征的通路水平特征和细胞过程。使用 TCGA 验证了模型的可泛化性和可解释性。我们为这些任务提出了一种分类系统,并建议将这种集成的人机学习方法应用于潜在的临床应用。一个公开的基于网络的平台实现了这些模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4779/10518635/c232e8fc6b49/fx1.jpg

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