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Noncoding RNAs and Deep Learning Neural Network Discriminate Multi-Cancer Types

SIMPLE SUMMARY: Imprecision and biases inherited in current cancer detection innovations hamper their applications at population level. Here, we employ deep learning neural networks and noncoding RNA biomarkers to develop an accurate cancer detection system to detect multiple cancer types. Our syste...

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Detalles Bibliográficos
Autores principales: Wang, Anyou, Hai, Rong, Rider, Paul J., He, Qianchuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8774129/
https://www.ncbi.nlm.nih.gov/pubmed/35053515
http://dx.doi.org/10.3390/cancers14020352
Descripción
Sumario:SIMPLE SUMMARY: Imprecision and biases inherited in current cancer detection innovations hamper their applications at population level. Here, we employ deep learning neural networks and noncoding RNA biomarkers to develop an accurate cancer detection system to detect multiple cancer types. Our system binarily classifies 26 common cancers vs. normal with >96% AUC, and it can become a practical cancer screening system at population level. ABSTRACT: Detecting cancers at early stages can dramatically reduce mortality rates. Therefore, practical cancer screening at the population level is needed. To develop a comprehensive detection system to classify multiple cancer types, we integrated an artificial intelligence deep learning neural network and noncoding RNA biomarkers selected from massive data. Our system can accurately detect cancer vs. healthy objects with 96.3% of AUC of ROC (Area Under Curve of a Receiver Operating Characteristic curve), and it surprisingly reaches 78.77% of AUC when validated by real-world raw data from a completely independent data set. Even validating with raw exosome data from blood, our system can reach 72% of AUC. Moreover, our system significantly outperforms conventional machine learning models, such as random forest. Intriguingly, with no more than six biomarkers, our approach can easily discriminate any individual cancer type vs. normal with 99% to 100% AUC. Furthermore, a comprehensive marker panel can simultaneously multi-classify common cancers with a stable 82.15% accuracy rate for heterogeneous cancerous tissues and conditions. This detection system provides a promising practical framework for automatic cancer screening at population level. Key points: (1) We developed a practical cancer screening system, which is simple, accurate, affordable, and easy to operate. (2) Our system binarily classify cancers vs. normal with >96% AUC. (3) In total, 26 individual cancer types can be easily detected by our system with 99 to 100% AUC. (4) The system can detect multiple cancer types simultaneously with >82% accuracy.