OncoTrace-TOO:使用转录组特征识别癌症组织起源的可解释机器学习框架

IF 1.9 Q4 ONCOLOGY
Cancer reports Pub Date : 2025-08-10 DOI:10.1002/cnr2.70311
Yang Hao, Haochun Huang, Daiyun Huang, Jianwen Ruan, Xin Liu, Jianquan Zhang
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引用次数: 0

摘要

原发未知的癌症仍然是一个巨大的诊断挑战,因为无法确定原发肿瘤的位置,这限制了靶向治疗的使用。尽管整合转录组学方法的机器学习方法为肿瘤起源提供了有价值的见解,但它们在区分生物学上相似的肿瘤时经常面临挑战,并且通常缺乏生物学可解释性。本研究旨在开发一个透明和生物学可解释的机器学习框架,以准确分类不同癌症类型的起源组织,从而促进临床诊断。方法设计基于基因表达谱的组织起源分类模型OncoTrace-TOO。该模型利用one-vs-rest差异表达分析识别出的泛癌鉴别分子特征,并采用逻辑回归作为分类算法。结果OncoTrace-TOO的总体准确率为0.967,对七种癌症类型(如CHOL、DLBC和LAML)进行了完美的分类。该模型在TCGA和GEO验证数据集上对原发性和转移性癌症都显示出很高的预测准确性,在解决组织学相关恶性肿瘤以及分类罕见癌症亚型方面具有增强的能力。应用于独立的临床肿瘤样本时,该模型的TOO预测准确率为0.857,进一步验证了其稳健性。重要的是,该框架通过揭示肿瘤特异性分子特征提供了生物学上可解释的预测,从而增强了其临床适用性。结论:OncoTrace-TOO不仅为组织起源分类提供了很高的预测准确性,而且还提供了生物学上有意义的见解,支持临床决策。这一框架有望提高诊断精度,并指导对具有挑战性的癌症病例进行个性化治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

OncoTrace-TOO: Interpretable Machine Learning Framework for Cancer Tissue-of-Origin Identification Using Transcriptomic Signatures

OncoTrace-TOO: Interpretable Machine Learning Framework for Cancer Tissue-of-Origin Identification Using Transcriptomic Signatures

Background

Cancer of unknown primary remains a formidable diagnostic challenge due to the inability to pinpoint the primary tumor site, which restricts the use of targeted therapeutics. Although machine-learning methods that integrate transcriptomic approaches have provided valuable insights into tumor origins, they often face challenges in distinguishing biologically similar tumors and typically lack biological interpretability.

Aims

This study aims to develop a transparent and biologically interpretable machine learning framework to accurately classify tissue-of-origin across diverse cancer types, thereby facilitation clinical diagnosis.

Methods

We designed OncoTrace-TOO, a novel tissue-of-origin classification model based on gene expression profiles. The model utilizes pan-cancer discriminative molecular features identified through one-vs-rest differential expression analysis and applies logistic regression as the classification algorithm.

Results

OncoTrace-TOO achieved an overall accuracy of 0.967, with perfect classification for seven cancer types (e.g., CHOL, DLBC, and LAML). The model demonstrated high predictive accuracy in both primary and metastatic cancers across TCGA and GEO validation datasets, with enhanced capability in resolving histologically related malignancies as well as classifying rare cancer subtypes. When applied to independent clinical tumor samples, the model achieved TOO prediction accuracies of 0.857, further validating its robustness. Importantly, the framework offers biologically interpretable predictions by revealing tumor-specific molecular signatures, thus enhancing its clinical applicability.

Conclusions

OncoTrace-TOO not only offers high predictive accuracy for tissue-of-origin classification, but also delivers biologically meaningful insights that support clinical decision-making. This framework holds promise for improving diagnostic precision and guiding personalized treatment in challenging cancer cases.

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来源期刊
Cancer reports
Cancer reports Medicine-Oncology
CiteScore
2.70
自引率
5.90%
发文量
160
审稿时长
17 weeks
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