4.7 Article

Multi-modal optimization to identify personalized biomarkers for disease prediction of individual patients with cancer

期刊

BRIEFINGS IN BIOINFORMATICS
卷 23, 期 5, 页码 -

出版社

OXFORD UNIV PRESS
DOI: 10.1093/bib/bbac254

关键词

multi-modal optimization; personalized biomarkers; tumor heterogeneity; disease prediction; drug targets

资金

  1. National Natural Science Foundation of China [62002329, 61922072, 61876169, 62106230]
  2. Key scientific and technological projects of Henan Province [212102310083, 212102210510]
  3. China Postdoctoral Foundation [2021M692915, 2021T140616, 2021M692920]
  4. Henan Postdoctoral Foundation [202002021]
  5. Research startup funds for top doctors in Zhengzhou University [32211739, 202003019]
  6. open Funds of the State Key Laboratory of Oncology in South China [HN2021-01]

向作者/读者索取更多资源

This study developed a novel model (MMPDNB) that can provide multiple personalized biomarker modules and uncover their multi-modal properties. By validating genomic data of breast or lung cancer patients, the experimental results demonstrated that MMPDNB can more effectively predict key states with the highest early warning signals during cancer development.
Finding personalized biomarkers for disease prediction of patients with cancer remains a massive challenge in precision medicine. Most methods focus on one subnetwork or module as a network biomarker; however, this ignores the early warning capabilities of other modules with different configurations of biomarkers (i.e. multi-modal personalized biomarkers). Identifying such modules would not only predict disease but also provide effective therapeutic drug target information for individual patients. To solve this problem, we developed a novel model (denoted multi-modal personalized dynamic network biomarkers (MMPDNB)) based on a multi-modal optimization mechanism and personalized dynamic network biomarker (PDNB) theory, which can provide multiple modules of personalized biomarkers and unveil their multi-modal properties. Using the genomics data of patients with breast or lung cancer from The Cancer Genome Atlas database, we validated the effectiveness of the MMPDNB model. The experimental results showed that compared with other advanced methods, MMPDNB can more effectively predict the critical state with the highest early warning signal score during cancer development. Furthermore, MMPDNB more significantly identified PDNBs containing driver and biomarker genes specific to cancer tissues. More importantly, we validated the biological significance of multi-modal PDNBs, which could provide effective drug targets of individual patients as well as markers for predicting early warning signals of the critical disease state. In conclusion, multi-modal optimization is an effective method to identify PDNBs and offers a new perspective for understanding tumor heterogeneity in cancer precision medicine.

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