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Published on: May 27, 2021
TARSL: Triple-Attention Cross-Network Representation Learning to Predict Synthetic Lethality for Anti-Cancer Drug
Abstract:
Cancer is a multifaceted disease that results from co-mutations of multi biological molecules. A promising strategy for cancer therapy involves in exploiting the phenomenon of Synthetic Lethality (SL) by targeting the SL partner of cancer gene. Since traditional methods for SL prediction suffer from high-cost, time-consuming and off-targets effects, computational approaches have been efficient complementary to these methods. Most of existing approaches treat SL associations as independent of other biological interaction networks, and fail to consider other information from various biological networks. Despite some approaches have integrated different networks to capture multi-modal features of genes for SL prediction, these methods implicitly assume that all sources and levels of information contribute equally to the SL associations. As such, a comprehensive and flexible framework for learning gene cross-network representations for SL prediction is still lacking. In this work, we present a novel Triple-Attention cross-network Representation learning for SL prediction (TARSL) by capturing molecular features from heterogeneous sources. We employ three-level attention modules to consider the different contribution of multi-level information. In particular, feature-level attention can capture the correlations between molecular feature and network link, node-level attention can differentiate the importance of various neighbors, and network-level attention can concentrate on important network and reduce the effects of irrelated networks. We perform comprehensive experiments on human SL datasets and these results have proven that our model is consistently superior to baseline methods and predicted SL associations could aid in designing anti-cancer drugs.
Insights
This study introduces a new computational method, Triple-Attention cross-network Representation learning (TARSL), for predicting synthetic lethality (SL) in cancer. TARSL effectively integrates diverse biological network data, improving cancer drug discovery by identifying key gene interactions.
Area of Science:
- Computational Biology
- Genomics
- Bioinformatics
Background:
- Cancer arises from complex genetic mutations, making synthetic lethality (SL) a promising therapeutic target.
- Traditional SL prediction methods are costly and time-consuming; computational approaches offer an efficient alternative.
- Existing computational methods often fail to integrate diverse biological network data effectively for SL prediction.
Purpose of the Study:
- To develop a novel computational framework for predicting synthetic lethality (SL) associations.
- To address the limitations of existing methods by integrating multi-modal biological network information.
- To create a flexible representation learning model for enhanced SL prediction.
Main Methods:
- Developed Triple-Attention cross-network Representation learning (TARSL) model.
- Employed three-level attention mechanisms: feature-level, node-level, and network-level attention.
- Integrated heterogeneous biological data sources for comprehensive gene representation learning.
Main Results:
- The TARSL model demonstrated superior performance compared to existing baseline methods on human SL datasets.
- The attention modules effectively captured varying contributions from multi-level information and biological networks.
- Predicted SL associations show potential for guiding the development of novel anti-cancer drugs.
Conclusions:
- The proposed TARSL model offers a significant advancement in computational prediction of synthetic lethality.
- Integrating multi-modal biological networks with attention mechanisms enhances the accuracy of SL prediction.
- This approach holds promise for accelerating the discovery of targeted cancer therapies.
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