Evidence map›Paper›PMID 36645245›Full record

ArticleBioinformatics (Oxford, England)2023

SLGNN: synthetic lethality prediction in human cancers based on factor-aware knowledge graph neural network.

Yan Zhu, Yuhuan Zhou, Yang Liu, Xuan Wang, Junyi Li

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

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0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

Who cites it

14 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Yan ZhuSchool of Computer Science and Technology, Harbin Institute of Technology (Shenzhen), Shenzhen 518055, China.
Yuhuan ZhouSchool of Computer Science and Technology, Harbin Institute of Technology (Shenzhen), Shenzhen 518055, China.
Yang LiuSchool of Computer Science and Technology, Harbin Institute of Technology (Shenzhen), Shenzhen 518055, China.ORCID 0000-0003-2486-5765
Xuan WangSchool of Computer Science and Technology, Harbin Institute of Technology (Shenzhen), Shenzhen 518055, China.
Junyi LiSchool of Computer Science and Technology, Harbin Institute of Technology (Shenzhen), Shenzhen 518055, China.ORCID 0000-0001-8045-5264

Funding

National Key R&D Program of China 2021YFA0910700
6 · The paper itself

Abstract

motivationSynthetic lethality (SL) is a form of genetic interaction that can selectively kill cancer cells without damaging normal cells. Exploiting this mechanism is gaining popularity in the field of targeted cancer therapy and anticancer drug development. Due to the limitations of identifying SL interactions from laboratory experiments, an increasing number of research groups are devising computational prediction methods to guide the discovery of potential SL pairs. Although existing methods have attempted to capture the underlying mechanisms of SL interactions, methods that have a deeper understanding of and attempt to explain SL mechanisms still need to be developed.

resultsIn this work, we propose a novel SL prediction method, SLGNN. This method is based on the following assumption: SL interactions are caused by different molecular events or biological processes, which we define as SL-related factors that lead to SL interactions. SLGNN, apart from identifying SL interaction pairs, also models the preferences of genes for different SL-related factors, making the results more interpretable for biologists and clinicians. SLGNN consists of three steps: first, we model the combinations of relationships in the gene-related knowledge graph as the SL-related factors. Next, we derive initial embeddings of genes through an explicit message aggregation process of the knowledge graph. Finally, we derive the final gene embeddings through an SL graph, constructed using known SL gene pairs, utilizing factor-based message aggregation. At this stage, a supervised end-to-end training model is used for SL interaction prediction. Based on experimental results, the proposed SLGNN model outperforms all current state-of-the-art SL prediction methods and provides better interpretability. AVAILABILITY AND IMPLEMENTATION: SLGNN is freely available at https://github.com/zy972014452/SLGNN.

Indexed as

NeoplasmsSynthetic Lethal MutationsDrug DevelopmentHumansNeural Networks, ComputerPattern Recognition, Automated

Identifiers

PMID36645245
PMCPMC9907046

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.