Multi-view graph convolutional network for cancer cell-specific synthetic lethality prediction

Kunjie Fan1, Shan Tang2, Birkan Gökbağ1

  • 1Department of Biomedical Informatics, The Ohio State University, Columbus, OH, United States.

Frontiers in Genetics
|January 26, 2023
PubMed

Insights

This study introduces MVGCN-iSL, a new computational model for identifying cancer-specific synthetic lethal (SL) gene pairs. It improves targeted cancer therapy research by predicting SL interactions more accurately using multi-omics data.

Area of Science:

  • Computational biology
  • Genomics
  • Bioinformatics

Background:

  • Synthetic lethal (SL) interactions are crucial for developing targeted cancer therapies.
  • Wet-lab screening for SL gene pairs is time-consuming and expensive.
  • Existing computational methods, including graph neural networks (GNNs), often lack cancer cell specificity and fail to fully leverage diverse biological features.

Purpose of the Study:

  • To develop a novel computational method for predicting cancer cell-specific SL gene pairs.
  • To improve the accuracy and efficiency of identifying potential therapeutic targets for cancer.

Main Methods:

  • Proposed MVGCN-iSL, a multi-view graph convolutional network (GCN) model.
  • Integrated five biological graph features and multi-omics data.
  • Utilized max pooling for integrating GCN representations and a deep neural network (DNN) for prediction of cancer cell-specific SL interactions (iSL).

Main Results:

  • MVGCN-iSL successfully integrated multiple graph features and multi-omics data.
  • The model achieved state-of-the-art performance in predicting SL gene pairs.
  • Demonstrated strong generalization ability to novel genes.

Conclusions:

  • MVGCN-iSL offers a powerful computational approach for discovering cancer cell-specific SL interactions.
  • The model enhances the potential for developing targeted cancer therapeutics.
  • Highlights the importance of integrating diverse biological features for improved predictive accuracy.

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