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Using graph-based model to identify cell specific synthetic lethal effects

Synthetic lethal (SL) pairs are pairs of genes whose simultaneous loss-of-function results in cell death, while a damaging mutation of either gene alone does not affect the cell’s survival. This makes SL pairs attractive targets for precision cancer therapies, as targeting the unimpaired gene of the...

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Autores principales: Pu, Mengchen, Cheng, Kaiyang, Li, Xiaorong, Xin, Yucui, Wei, Lanying, Jin, Sutong, Zheng, Weisheng, Peng, Gongxin, Tang, Qihong, Zhou, Jielong, Zhang, Yingsheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research Network of Computational and Structural Biotechnology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10618116/
https://www.ncbi.nlm.nih.gov/pubmed/37920819
http://dx.doi.org/10.1016/j.csbj.2023.10.011
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author Pu, Mengchen
Cheng, Kaiyang
Li, Xiaorong
Xin, Yucui
Wei, Lanying
Jin, Sutong
Zheng, Weisheng
Peng, Gongxin
Tang, Qihong
Zhou, Jielong
Zhang, Yingsheng
author_facet Pu, Mengchen
Cheng, Kaiyang
Li, Xiaorong
Xin, Yucui
Wei, Lanying
Jin, Sutong
Zheng, Weisheng
Peng, Gongxin
Tang, Qihong
Zhou, Jielong
Zhang, Yingsheng
author_sort Pu, Mengchen
collection PubMed
description Synthetic lethal (SL) pairs are pairs of genes whose simultaneous loss-of-function results in cell death, while a damaging mutation of either gene alone does not affect the cell’s survival. This makes SL pairs attractive targets for precision cancer therapies, as targeting the unimpaired gene of the SL pair can selectively kill cancer cells that already harbor the impaired gene. Limited by the difficulty of finding true SL pairs, especially on specific cell types, current computational approaches provide only limited insights because of overlooking the crucial aspects of cellular context dependency and mechanistic understanding of SL pairs. As a result, the identification of SL targets still relies on expensive, time-consuming experimental approaches. In this work, we applied cell-line specific multi-omics data to a specially designed deep learning model to predict cell-line specific SL pairs. Through incorporating multiple types of cell-specific omics data with a self-attention module, we represent gene relationships as graphs. Our approach achieves the prediction of SL pairs in a cell-specific manner and demonstrates the potential to facilitate the discovery of cell-specific SL targets for cancer therapeutics, providing a tool to unearth mechanisms underlying the origin of SL in cancer biology. The code and data of our approach can be found at https://github.com/promethiume/SLwise
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spelling pubmed-106181162023-11-02 Using graph-based model to identify cell specific synthetic lethal effects Pu, Mengchen Cheng, Kaiyang Li, Xiaorong Xin, Yucui Wei, Lanying Jin, Sutong Zheng, Weisheng Peng, Gongxin Tang, Qihong Zhou, Jielong Zhang, Yingsheng Comput Struct Biotechnol J Method Article Synthetic lethal (SL) pairs are pairs of genes whose simultaneous loss-of-function results in cell death, while a damaging mutation of either gene alone does not affect the cell’s survival. This makes SL pairs attractive targets for precision cancer therapies, as targeting the unimpaired gene of the SL pair can selectively kill cancer cells that already harbor the impaired gene. Limited by the difficulty of finding true SL pairs, especially on specific cell types, current computational approaches provide only limited insights because of overlooking the crucial aspects of cellular context dependency and mechanistic understanding of SL pairs. As a result, the identification of SL targets still relies on expensive, time-consuming experimental approaches. In this work, we applied cell-line specific multi-omics data to a specially designed deep learning model to predict cell-line specific SL pairs. Through incorporating multiple types of cell-specific omics data with a self-attention module, we represent gene relationships as graphs. Our approach achieves the prediction of SL pairs in a cell-specific manner and demonstrates the potential to facilitate the discovery of cell-specific SL targets for cancer therapeutics, providing a tool to unearth mechanisms underlying the origin of SL in cancer biology. The code and data of our approach can be found at https://github.com/promethiume/SLwise Research Network of Computational and Structural Biotechnology 2023-10-09 /pmc/articles/PMC10618116/ /pubmed/37920819 http://dx.doi.org/10.1016/j.csbj.2023.10.011 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Method Article
Pu, Mengchen
Cheng, Kaiyang
Li, Xiaorong
Xin, Yucui
Wei, Lanying
Jin, Sutong
Zheng, Weisheng
Peng, Gongxin
Tang, Qihong
Zhou, Jielong
Zhang, Yingsheng
Using graph-based model to identify cell specific synthetic lethal effects
title Using graph-based model to identify cell specific synthetic lethal effects
title_full Using graph-based model to identify cell specific synthetic lethal effects
title_fullStr Using graph-based model to identify cell specific synthetic lethal effects
title_full_unstemmed Using graph-based model to identify cell specific synthetic lethal effects
title_short Using graph-based model to identify cell specific synthetic lethal effects
title_sort using graph-based model to identify cell specific synthetic lethal effects
topic Method Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10618116/
https://www.ncbi.nlm.nih.gov/pubmed/37920819
http://dx.doi.org/10.1016/j.csbj.2023.10.011
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