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Cancers Originate from Somatic Mutations in a Single Cell02:21

Cancers Originate from Somatic Mutations in a Single Cell

Cancer arises from mutations in the critical genes that allow healthy cells to escape cell cycle regulation and acquire the ability to proliferate indefinitely. Though originating from a single mutation event in one of the originator cells, cancer progresses when the mutant cell lines continue to gain more and more mutations, and finally, become malignant. For example, chronic myelogenous leukemia (CML) develops initially as a non-lethal increase in white blood cells, which progressively...
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Federated Deep Learning Enables Cancer Subtyping by Proteomics.

Zhaoxiang Cai1, Emma L Boys1, Zainab Noor1

  • 1ProCan, Children's Medical Research Institute, Faculty of Medicine and Health, The University of Sydney, Westmead, Australia.

Cancer Discovery
|June 9, 2025
PubMed
Summary
This summary is machine-generated.

Federated deep learning (ProCanFDL) enables artificial intelligence model training on sensitive proteomic data without compromising privacy. This approach significantly improves cancer subtyping accuracy and facilitates global collaboration for biomarker discovery.

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Area of Science:

  • Biomedicine
  • Artificial Intelligence
  • Proteomics
  • Machine Learning

Background:

  • Artificial intelligence (AI) in biomedicine is hindered by stringent data privacy regulations.
  • Clinically annotated tissue proteomic data presents unique privacy challenges.
  • Developing large-scale AI models requires access to diverse, multi-institutional datasets.

Purpose of the Study:

  • To develop a privacy-preserving federated deep learning approach for analyzing tissue proteomic data.
  • To address the challenge of data privacy in AI applications within biomedicine.
  • To enable international collaboration for proteomic data analysis and biomarker discovery.

Main Methods:

  • Developed ProCanFDL, a federated deep learning framework.
  • Trained local models on simulated and private firewall-protected proteomic datasets (pan-cancer and 29 cohorts).
  • Aggregated local model updates to create a global model, validated on hold-out and external datasets.

Main Results:

  • ProCanFDL achieved a 43% performance gain in 14 cancer subtyping tasks compared to local models.
  • The federated approach matched the performance of a centralized model.
  • Demonstrated generalizability by retraining on diverse external proteomic datasets (DIA-MS and TMT proteomics).

Conclusions:

  • ProCanFDL offers a viable solution for privacy-compliant machine learning with proteomic data.
  • Enables collaborative initiatives for biomarker and treatment target discovery.
  • Facilitates the development of large-scale, privacy-preserving AI models, including foundation models, across global institutions.