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Dynamic cancer drivers: a causal approach for cancer driver discovery based on bio-pathological trajectories

The traditional way for discovering genes which drive cancer (namely cancer drivers) neglects the dynamic information of cancer development, even though it is well known that cancer progresses dynamically. To enhance cancer driver discovery, we expand cancer driver concept to dynamic cancer driver a...

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Autores principales: Cifuentes-Bernal, Andres M, Pham, Vu V H, Li, Xiaomei, Liu, Lin, Li, Jiuyong, Duy Le, Thuc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10467634/
https://www.ncbi.nlm.nih.gov/pubmed/36124841
http://dx.doi.org/10.1093/bfgp/elac030
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author Cifuentes-Bernal, Andres M
Pham, Vu V H
Li, Xiaomei
Liu, Lin
Li, Jiuyong
Duy Le, Thuc
author_facet Cifuentes-Bernal, Andres M
Pham, Vu V H
Li, Xiaomei
Liu, Lin
Li, Jiuyong
Duy Le, Thuc
author_sort Cifuentes-Bernal, Andres M
collection PubMed
description The traditional way for discovering genes which drive cancer (namely cancer drivers) neglects the dynamic information of cancer development, even though it is well known that cancer progresses dynamically. To enhance cancer driver discovery, we expand cancer driver concept to dynamic cancer driver as a gene driving one or more bio-pathological transitions during cancer progression. Our method refers to the fact that cancer should not be considered as a single process but a compendium of altered biological processes causing the disease to develop over time. Reciprocally, different drivers of cancer can potentially be discovered by analysing different bio-pathological pathways. We propose a novel approach for causal inference of genes driving one or more core processes during cancer development (i.e. dynamic cancer driver). We use the concept of pseudotime for inferring the latent progression of samples along a biological transition during cancer and identifying a critical event when such a process is significantly deviated from normal to carcinogenic. We infer driver genes by assessing the causal effect they have on the process after such a critical event. We have applied our method to single-cell and bulk sequencing datasets of breast cancer. The evaluation results show that our method outperforms well-recognized cancer driver inference methods. These results suggest that including information of the underlying dynamics of cancer improves the inference process (in comparison with using static data), and allows us to discover different sets of driver genes from different processes in cancer. R scripts and datasets can be found at https://github.com/AndresMCB/DynamicCancerDriver
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spelling pubmed-104676342023-08-31 Dynamic cancer drivers: a causal approach for cancer driver discovery based on bio-pathological trajectories Cifuentes-Bernal, Andres M Pham, Vu V H Li, Xiaomei Liu, Lin Li, Jiuyong Duy Le, Thuc Brief Funct Genomics Protocol Article The traditional way for discovering genes which drive cancer (namely cancer drivers) neglects the dynamic information of cancer development, even though it is well known that cancer progresses dynamically. To enhance cancer driver discovery, we expand cancer driver concept to dynamic cancer driver as a gene driving one or more bio-pathological transitions during cancer progression. Our method refers to the fact that cancer should not be considered as a single process but a compendium of altered biological processes causing the disease to develop over time. Reciprocally, different drivers of cancer can potentially be discovered by analysing different bio-pathological pathways. We propose a novel approach for causal inference of genes driving one or more core processes during cancer development (i.e. dynamic cancer driver). We use the concept of pseudotime for inferring the latent progression of samples along a biological transition during cancer and identifying a critical event when such a process is significantly deviated from normal to carcinogenic. We infer driver genes by assessing the causal effect they have on the process after such a critical event. We have applied our method to single-cell and bulk sequencing datasets of breast cancer. The evaluation results show that our method outperforms well-recognized cancer driver inference methods. These results suggest that including information of the underlying dynamics of cancer improves the inference process (in comparison with using static data), and allows us to discover different sets of driver genes from different processes in cancer. R scripts and datasets can be found at https://github.com/AndresMCB/DynamicCancerDriver Oxford University Press 2022-09-19 /pmc/articles/PMC10467634/ /pubmed/36124841 http://dx.doi.org/10.1093/bfgp/elac030 Text en © The Author(s) 2022. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Protocol Article
Cifuentes-Bernal, Andres M
Pham, Vu V H
Li, Xiaomei
Liu, Lin
Li, Jiuyong
Duy Le, Thuc
Dynamic cancer drivers: a causal approach for cancer driver discovery based on bio-pathological trajectories
title Dynamic cancer drivers: a causal approach for cancer driver discovery based on bio-pathological trajectories
title_full Dynamic cancer drivers: a causal approach for cancer driver discovery based on bio-pathological trajectories
title_fullStr Dynamic cancer drivers: a causal approach for cancer driver discovery based on bio-pathological trajectories
title_full_unstemmed Dynamic cancer drivers: a causal approach for cancer driver discovery based on bio-pathological trajectories
title_short Dynamic cancer drivers: a causal approach for cancer driver discovery based on bio-pathological trajectories
title_sort dynamic cancer drivers: a causal approach for cancer driver discovery based on bio-pathological trajectories
topic Protocol Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10467634/
https://www.ncbi.nlm.nih.gov/pubmed/36124841
http://dx.doi.org/10.1093/bfgp/elac030
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