Combining Spatial Transcriptomics, Pseudotime, and Machine Learning Enables Discovery of Biomarkers for Prostate Cancer

前列腺癌 癌症 生物标志物发现 转录组 前列腺 生物标志物 计算生物学 医学 蛋白质组学 生物信息学 计算机科学 病理 肿瘤科 内科学 生物 基因 基因表达 生物化学
作者
Martin Smelik,Daniel Diaz-Roncero Gonzalez,Xiaojing An,Rakesh Heer,Lars Henningsohn,Xinxiu Li,Hui Wang,Yelin Zhao,Mikael Benson
出处
期刊:Cancer Research [American Association for Cancer Research]
卷期号:85 (13): 2514-2526 被引量:15
标识
DOI:10.1158/0008-5472.can-25-0269
摘要

Early cancer diagnosis is crucial but challenging owing to the lack of reliable biomarkers that can be measured using routine clinical methods. The identification of biomarkers for early detection is complicated by each tumor involving changes in the interactions between thousands of genes. In addition to this staggering complexity, these interactions can vary among patients with the same diagnosis as well as within the same tumor. We hypothesized that reliable biomarkers that can be measured with routine methods could be identified by exploiting three facts: (i) the same tumor can have multiple grades of malignant transformation; (ii) these grades and their molecular changes can be characterized using spatial transcriptomics; and (iii) these changes can be integrated into models of malignant transformation using pseudotime. Pseudotime models were constructed based on spatial transcriptomic data from three independent prostate cancer studies to prioritize the genes that were most correlated with malignant transformation. The identified genes were associated with cancer grade, copy-number aberrations, hallmark pathways, and drug targets, and they encoded candidate biomarkers for prostate cancer in mRNA, IHC, and proteomics data from the sera, prostate tissue, and urine of more than 2,000 patients with prostate cancer and controls. Machine learning-based prediction models revealed that the biomarkers in urine had an AUC of 0.92 for prostate cancer and were associated with cancer grade. Overall, this study demonstrates the diagnostic potential of combining spatial transcriptomics, pseudotime, and machine learning for prostate cancer, which should be further tested in prospective studies. SIGNIFICANCE: Integrating spatial transcriptomics, pseudotime, and machine learning analyses is effective for identifying prostate cancer biomarkers that are reliable in different settings and measurable with routine methods, providing potential early diagnosis strategies. This article is part of a special series: Driving Cancer Discoveries with Computational Research, Data Science, and Machine Learning/AI.
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