Deep generative AI models analyzing circulating orphan non-coding RNAs enable detection of early-stage lung cancer

被引:2
|
作者
Karimzadeh, Mehran [1 ]
Momen-Roknabadi, Amir [1 ]
Cavazos, Taylor B. [1 ]
Fang, Yuqi [1 ]
Chen, Nae-Chyun [1 ]
Multhaup, Michael [1 ]
Yen, Jennifer [1 ]
Ku, Jeremy [1 ]
Wang, Jieyang [1 ]
Zhao, Xuan [1 ]
Murzynowski, Philip [1 ]
Wang, Kathleen [1 ]
Hanna, Rose [1 ]
Huang, Alice [1 ]
Corti, Diana [1 ]
Nguyen, Dang [1 ]
Lam, Ti [1 ]
Kilinc, Seda [1 ]
Arensdorf, Patrick [1 ]
Chau, Kimberly H. [1 ]
Hartwig, Anna [1 ]
Fish, Lisa [1 ]
Li, Helen [1 ]
Behsaz, Babak [1 ]
Elemento, Olivier [2 ]
Zou, James [3 ]
Hormozdiari, Fereydoun [1 ,4 ]
Alipanahi, Babak [1 ]
Goodarzi, Hani [5 ,6 ]
机构
[1] Exai Bio Inc, Palo Alto, CA 94303 USA
[2] Weill Cornell Med, New York, NY USA
[3] Stanford Univ, Stanford, CA USA
[4] Univ Calif Davis, Davis, CA 95616 USA
[5] Univ Calif San Francisco, San Francisco, CA 94143 USA
[6] Arc Inst, Palo Alto, CA 94304 USA
关键词
D O I
10.1038/s41467-024-53851-9
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Liquid biopsies have the potential to revolutionize cancer care through non-invasive early detection of tumors. Developing a robust liquid biopsy test requires collecting high-dimensional data from a large number of blood samples across heterogeneous groups of patients. We propose that the generative capability of variational auto-encoders enables learning a robust and generalizable signature of blood-based biomarkers. In this study, we analyze orphan non-coding RNAs (oncRNAs) from serum samples of 1050 individuals diagnosed with non-small cell lung cancer (NSCLC) at various stages, as well as sex-, age-, and BMI-matched controls. We demonstrate that our multi-task generative AI model, Orion, surpasses commonly used methods in both overall performance and generalizability to held-out datasets. Orion achieves an overall sensitivity of 94% (95% CI: 87%-98%) at 87% (95% CI: 81%-93%) specificity for cancer detection across all stages, outperforming the sensitivity of other methods on held-out validation datasets by more than similar to 30%.
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页数:12
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