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精准肿瘤学超越靶向治疗:将组学数据与机器学习相结合,使大多数癌细胞与有效的治疗方法相匹配。

Precision Oncology beyond Targeted Therapy: Combining Omics Data with Machine Learning Matches the Majority of Cancer Cells to Effective Therapeutics.

机构信息

Department of Biomedical Informatics, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.

Center for Translational Bioinformatics, University of Pittsburgh, Pittsburgh, Pennsylvania.

出版信息

Mol Cancer Res. 2018 Feb;16(2):269-278. doi: 10.1158/1541-7786.MCR-17-0378. Epub 2017 Nov 13.

DOI:10.1158/1541-7786.MCR-17-0378
PMID:29133589
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5821274/
Abstract

Precision oncology involves identifying drugs that will effectively treat a tumor and then prescribing an optimal clinical treatment regimen. However, most first-line chemotherapy drugs do not have biomarkers to guide their application. For molecularly targeted drugs, using the genomic status of a drug target as a therapeutic indicator has limitations. In this study, machine learning methods (e.g., deep learning) were used to identify informative features from genome-scale omics data and to train classifiers for predicting the effectiveness of drugs in cancer cell lines. The methodology introduced here can accurately predict the efficacy of drugs, regardless of whether they are molecularly targeted or nonspecific chemotherapy drugs. This approach, on a per-drug basis, can identify sensitive cancer cells with an average sensitivity of 0.82 and specificity of 0.82; on a per-cell line basis, it can identify effective drugs with an average sensitivity of 0.80 and specificity of 0.82. This report describes a data-driven precision medicine approach that is not only generalizable but also optimizes therapeutic efficacy. The framework detailed herein, when successfully translated to clinical environments, could significantly broaden the scope of precision oncology beyond targeted therapies, benefiting an expanded proportion of cancer patients. .

摘要

精准肿瘤学涉及识别能够有效治疗肿瘤的药物,然后为患者制定最佳的临床治疗方案。然而,大多数一线化疗药物没有生物标志物来指导其应用。对于分子靶向药物,使用药物靶点的基因组状态作为治疗指标具有局限性。在这项研究中,使用机器学习方法(例如深度学习)从基因组规模的组学数据中识别信息特征,并训练分类器来预测药物在癌细胞系中的疗效。这里介绍的方法可以准确预测药物的疗效,无论这些药物是分子靶向药物还是非特异性化疗药物。这种基于药物的方法可以识别敏感性癌症细胞,平均敏感性为 0.82,特异性为 0.82;基于细胞系的方法可以识别有效药物,平均敏感性为 0.80,特异性为 0.82。本报告描述了一种数据驱动的精准医学方法,不仅具有通用性,而且还可以优化治疗效果。本文详细介绍的框架,如果成功转化为临床环境,可以将精准肿瘤学的范围大大扩展到靶向治疗之外,使更多比例的癌症患者受益。

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Palbociclib and Letrozole in Advanced Breast Cancer.帕博西尼联合来曲唑治疗晚期乳腺癌。
N Engl J Med. 2016 Nov 17;375(20):1925-1936. doi: 10.1056/NEJMoa1607303.
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Limits to Personalized Cancer Medicine.个性化癌症医学的局限性。
N Engl J Med. 2016 Sep 29;375(13):1289-94. doi: 10.1056/NEJMsb1607705.
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Perspective: The precision-oncology illusion.观点:精准肿瘤学的错觉。
ASGCL:用于癌症药物反应预测的基于自适应稀疏映射的图对比学习网络。
PLoS Comput Biol. 2025 Jan 30;21(1):e1012748. doi: 10.1371/journal.pcbi.1012748. eCollection 2025 Jan.
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A precision oncology-focused deep learning framework for personalized selection of cancer therapy.一种专注于精准肿瘤学的深度学习框架,用于个性化选择癌症治疗方案。
bioRxiv. 2024 Dec 16:2024.12.12.628190. doi: 10.1101/2024.12.12.628190.
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Learning chemical sensitivity reveals mechanisms of cellular response.学习化学敏感性揭示了细胞反应的机制。
Commun Biol. 2024 Sep 15;7(1):1149. doi: 10.1038/s42003-024-06865-4.
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iGenSig-Rx: an integral genomic signature based white-box tool for modeling cancer therapeutic responses using multi-omics data.iGenSig-Rx:一种基于整体基因组特征的白盒工具,用于使用多组学数据对癌症治疗反应进行建模。
BMC Bioinformatics. 2024 Jun 19;25(1):220. doi: 10.1186/s12859-024-05835-1.
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Identification of cancer risk groups through multi-omics integration using autoencoder and tensor analysis.通过自编码器和张量分析的多组学整合来识别癌症风险组。
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Improving Anticancer Drug Selection and Prioritization via Neural Learning to Rank.通过神经学习排序提高抗癌药物选择和优先级排序。
J Chem Inf Model. 2024 May 27;64(10):4071-4088. doi: 10.1021/acs.jcim.3c01060. Epub 2024 May 13.
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