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Identifying the critical state of cancers by single-sample Markov flow entropy

BACKGROUND: The progression of complex diseases sometimes undergoes a drastic critical transition, at which the biological system abruptly shifts from a relatively healthy state (before-transition stage) to a disease state (after-transition stage). Searching for such a critical transition or critica...

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Autores principales: Liu, Juntan, Tao, Yuan, Lan, Ruoqi, Zhong, Jiayuan, Liu, Rui, Chen, Pei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10373650/
https://www.ncbi.nlm.nih.gov/pubmed/37520244
http://dx.doi.org/10.7717/peerj.15695
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author Liu, Juntan
Tao, Yuan
Lan, Ruoqi
Zhong, Jiayuan
Liu, Rui
Chen, Pei
author_facet Liu, Juntan
Tao, Yuan
Lan, Ruoqi
Zhong, Jiayuan
Liu, Rui
Chen, Pei
author_sort Liu, Juntan
collection PubMed
description BACKGROUND: The progression of complex diseases sometimes undergoes a drastic critical transition, at which the biological system abruptly shifts from a relatively healthy state (before-transition stage) to a disease state (after-transition stage). Searching for such a critical transition or critical state is crucial to provide timely and effective scientific treatment to patients. However, in most conditions where only a small sample size of clinical data is available, resulting in failure when detecting the critical states of complex diseases, particularly only single-sample data. METHODS: In this study, different from traditional methods that require multiple samples at each time, a model-free computational method, single-sample Markov flow entropy (sMFE), provides a solution to the identification problem of critical states/pre-disease states of complex diseases, solely based on a single-sample. Our proposed method was employed to characterize the dynamic changes of complex diseases from the perspective of network entropy. RESULTS: The proposed approach was verified by unmistakably identifying the critical state just before the occurrence of disease deterioration for four tumor datasets from The Cancer Genome Atlas (TCGA) database. In addition, two new prognostic biomarkers, optimistic sMFE (O-sMFE) and pessimistic sMFE (P-sMFE) biomarkers, were identified by our method and enable the prognosis evaluation of tumors. CONCLUSIONS: The proposed method has shown its capability to accurately detect pre-disease states of four cancers and provide two novel prognostic biomarkers, O-sMFE and P-sMFE biomarkers, to facilitate the personalized prognosis of patients. This is a remarkable achievement that could have a major impact on the diagnosis and treatment of complex diseases.
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spelling pubmed-103736502023-07-28 Identifying the critical state of cancers by single-sample Markov flow entropy Liu, Juntan Tao, Yuan Lan, Ruoqi Zhong, Jiayuan Liu, Rui Chen, Pei PeerJ Bioinformatics BACKGROUND: The progression of complex diseases sometimes undergoes a drastic critical transition, at which the biological system abruptly shifts from a relatively healthy state (before-transition stage) to a disease state (after-transition stage). Searching for such a critical transition or critical state is crucial to provide timely and effective scientific treatment to patients. However, in most conditions where only a small sample size of clinical data is available, resulting in failure when detecting the critical states of complex diseases, particularly only single-sample data. METHODS: In this study, different from traditional methods that require multiple samples at each time, a model-free computational method, single-sample Markov flow entropy (sMFE), provides a solution to the identification problem of critical states/pre-disease states of complex diseases, solely based on a single-sample. Our proposed method was employed to characterize the dynamic changes of complex diseases from the perspective of network entropy. RESULTS: The proposed approach was verified by unmistakably identifying the critical state just before the occurrence of disease deterioration for four tumor datasets from The Cancer Genome Atlas (TCGA) database. In addition, two new prognostic biomarkers, optimistic sMFE (O-sMFE) and pessimistic sMFE (P-sMFE) biomarkers, were identified by our method and enable the prognosis evaluation of tumors. CONCLUSIONS: The proposed method has shown its capability to accurately detect pre-disease states of four cancers and provide two novel prognostic biomarkers, O-sMFE and P-sMFE biomarkers, to facilitate the personalized prognosis of patients. This is a remarkable achievement that could have a major impact on the diagnosis and treatment of complex diseases. PeerJ Inc. 2023-07-24 /pmc/articles/PMC10373650/ /pubmed/37520244 http://dx.doi.org/10.7717/peerj.15695 Text en © 2023 Liu et al. 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 use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Bioinformatics
Liu, Juntan
Tao, Yuan
Lan, Ruoqi
Zhong, Jiayuan
Liu, Rui
Chen, Pei
Identifying the critical state of cancers by single-sample Markov flow entropy
title Identifying the critical state of cancers by single-sample Markov flow entropy
title_full Identifying the critical state of cancers by single-sample Markov flow entropy
title_fullStr Identifying the critical state of cancers by single-sample Markov flow entropy
title_full_unstemmed Identifying the critical state of cancers by single-sample Markov flow entropy
title_short Identifying the critical state of cancers by single-sample Markov flow entropy
title_sort identifying the critical state of cancers by single-sample markov flow entropy
topic Bioinformatics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10373650/
https://www.ncbi.nlm.nih.gov/pubmed/37520244
http://dx.doi.org/10.7717/peerj.15695
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