An Integrated View of Virus-Triggered Cellular Plasticity Using Boolean Networks

ABSTRACT: Virus-related mortality and morbidity are due to cell/tissue damage caused by replicative pressure and resource exhaustion, e.g., HBV or HIV; exaggerated immune responses, e.g., SARSCoV-2; and cancer, e.g., EBV or HPV. In this context, oncogenic and other types of viruses drive genetic and...

Full description

Autores:
Granados Alzate, María Camila
Alfaro García, Jenny Paola
Gallego Gómez, Juan Carlos
Vicente Manzanares, Miguel
Tipo de recurso:
Review article
Fecha de publicación:
2021
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/45426
Acceso en línea:
https://hdl.handle.net/10495/45426
Palabra clave:
Cell Plasticity
Plasticidad de la Célula
Cellular Reprogramming
Reprogramación Celular
Epithelial-Mesenchymal Transition
Transición Epitelial-Mesenquimal
Gene Regulatory Networks
Redes Reguladoras de Genes
Neoplasms
Neoplasias
Systems Biology
Biología de Sistemas
Virus Diseases
Virosis
Viruses
Virus
https://id.nlm.nih.gov/mesh/D014780
https://id.nlm.nih.gov/mesh/D000066670
https://id.nlm.nih.gov/mesh/D065150
https://id.nlm.nih.gov/mesh/D058750
https://id.nlm.nih.gov/mesh/D053263
https://id.nlm.nih.gov/mesh/D009369
https://id.nlm.nih.gov/mesh/D049490
https://id.nlm.nih.gov/mesh/D014777
Rights
openAccess
License
https://creativecommons.org/licenses/by/4.0/
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dc.title.spa.fl_str_mv An Integrated View of Virus-Triggered Cellular Plasticity Using Boolean Networks
title An Integrated View of Virus-Triggered Cellular Plasticity Using Boolean Networks
spellingShingle An Integrated View of Virus-Triggered Cellular Plasticity Using Boolean Networks
Cell Plasticity
Plasticidad de la Célula
Cellular Reprogramming
Reprogramación Celular
Epithelial-Mesenchymal Transition
Transición Epitelial-Mesenquimal
Gene Regulatory Networks
Redes Reguladoras de Genes
Neoplasms
Neoplasias
Systems Biology
Biología de Sistemas
Virus Diseases
Virosis
Viruses
Virus
https://id.nlm.nih.gov/mesh/D014780
https://id.nlm.nih.gov/mesh/D000066670
https://id.nlm.nih.gov/mesh/D065150
https://id.nlm.nih.gov/mesh/D058750
https://id.nlm.nih.gov/mesh/D053263
https://id.nlm.nih.gov/mesh/D009369
https://id.nlm.nih.gov/mesh/D049490
https://id.nlm.nih.gov/mesh/D014777
title_short An Integrated View of Virus-Triggered Cellular Plasticity Using Boolean Networks
title_full An Integrated View of Virus-Triggered Cellular Plasticity Using Boolean Networks
title_fullStr An Integrated View of Virus-Triggered Cellular Plasticity Using Boolean Networks
title_full_unstemmed An Integrated View of Virus-Triggered Cellular Plasticity Using Boolean Networks
title_sort An Integrated View of Virus-Triggered Cellular Plasticity Using Boolean Networks
dc.creator.fl_str_mv Granados Alzate, María Camila
Alfaro García, Jenny Paola
Gallego Gómez, Juan Carlos
Vicente Manzanares, Miguel
dc.contributor.author.none.fl_str_mv Granados Alzate, María Camila
Alfaro García, Jenny Paola
Gallego Gómez, Juan Carlos
Vicente Manzanares, Miguel
dc.contributor.researchgroup.spa.fl_str_mv Grupo Medicina Molecular y de Translación
dc.subject.decs.none.fl_str_mv Cell Plasticity
Plasticidad de la Célula
Cellular Reprogramming
Reprogramación Celular
Epithelial-Mesenchymal Transition
Transición Epitelial-Mesenquimal
Gene Regulatory Networks
Redes Reguladoras de Genes
Neoplasms
Neoplasias
Systems Biology
Biología de Sistemas
Virus Diseases
Virosis
Viruses
Virus
topic Cell Plasticity
Plasticidad de la Célula
Cellular Reprogramming
Reprogramación Celular
Epithelial-Mesenchymal Transition
Transición Epitelial-Mesenquimal
Gene Regulatory Networks
Redes Reguladoras de Genes
Neoplasms
Neoplasias
Systems Biology
Biología de Sistemas
Virus Diseases
Virosis
Viruses
Virus
https://id.nlm.nih.gov/mesh/D014780
https://id.nlm.nih.gov/mesh/D000066670
https://id.nlm.nih.gov/mesh/D065150
https://id.nlm.nih.gov/mesh/D058750
https://id.nlm.nih.gov/mesh/D053263
https://id.nlm.nih.gov/mesh/D009369
https://id.nlm.nih.gov/mesh/D049490
https://id.nlm.nih.gov/mesh/D014777
dc.subject.lcshuri.none.fl_str_mv https://id.nlm.nih.gov/mesh/D014780
dc.subject.meshuri.none.fl_str_mv https://id.nlm.nih.gov/mesh/D000066670
https://id.nlm.nih.gov/mesh/D065150
https://id.nlm.nih.gov/mesh/D058750
https://id.nlm.nih.gov/mesh/D053263
https://id.nlm.nih.gov/mesh/D009369
https://id.nlm.nih.gov/mesh/D049490
https://id.nlm.nih.gov/mesh/D014777
description ABSTRACT: Virus-related mortality and morbidity are due to cell/tissue damage caused by replicative pressure and resource exhaustion, e.g., HBV or HIV; exaggerated immune responses, e.g., SARSCoV-2; and cancer, e.g., EBV or HPV. In this context, oncogenic and other types of viruses drive genetic and epigenetic changes that expand the tumorigenic program, including modifications to the ability of cancer cells to migrate. The best-characterized group of changes is collectively known as the epithelial–mesenchymal transition, or EMT. This is a complex phenomenon classically described using biochemistry, cell biology and genetics. However, these methods require enormous, often slow, efforts to identify and validate novel therapeutic targets. Systems biology can complement and accelerate discoveries in this field. One example of such an approach is Boolean networks, which make complex biological problems tractable by modeling data (“nodes”) connected by logical operators. Here, we focus on virus-induced cellular plasticity and cell reprogramming in mammals, and how Boolean networks could provide novel insights into the ability of some viruses to trigger uncontrolled cell proliferation and EMT, two key hallmarks of cancer.
publishDate 2021
dc.date.issued.none.fl_str_mv 2021
dc.date.accessioned.none.fl_str_mv 2025-03-09T12:40:39Z
dc.date.available.none.fl_str_mv 2025-03-09T12:40:39Z
dc.type.spa.fl_str_mv Artículo de revisión
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dc.identifier.citation.spa.fl_str_mv Alfaro-García JP, Granados-Alzate MC, Vicente-Manzanares M, Gallego-Gómez JC. An Integrated View of Virus-Triggered Cellular Plasticity Using Boolean Networks. Cells. 2021 Oct 24;10(11):2863. doi: 10.3390/cells10112863.
dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/10495/45426
dc.identifier.doi.none.fl_str_mv 10.3390/cells10112863
dc.identifier.eissn.none.fl_str_mv 2073-4409
identifier_str_mv Alfaro-García JP, Granados-Alzate MC, Vicente-Manzanares M, Gallego-Gómez JC. An Integrated View of Virus-Triggered Cellular Plasticity Using Boolean Networks. Cells. 2021 Oct 24;10(11):2863. doi: 10.3390/cells10112863.
10.3390/cells10112863
2073-4409
url https://hdl.handle.net/10495/45426
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.ispartofjournalabbrev.spa.fl_str_mv Cells
dc.relation.citationendpage.spa.fl_str_mv 15
dc.relation.citationissue.spa.fl_str_mv 11
dc.relation.citationstartpage.spa.fl_str_mv 1
dc.relation.citationvolume.spa.fl_str_mv 10
dc.relation.ispartofjournal.spa.fl_str_mv Cells
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institution Universidad de Antioquia
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spelling Granados Alzate, María CamilaAlfaro García, Jenny PaolaGallego Gómez, Juan CarlosVicente Manzanares, MiguelGrupo Medicina Molecular y de Translación2025-03-09T12:40:39Z2025-03-09T12:40:39Z2021Alfaro-García JP, Granados-Alzate MC, Vicente-Manzanares M, Gallego-Gómez JC. An Integrated View of Virus-Triggered Cellular Plasticity Using Boolean Networks. Cells. 2021 Oct 24;10(11):2863. doi: 10.3390/cells10112863.https://hdl.handle.net/10495/4542610.3390/cells101128632073-4409ABSTRACT: Virus-related mortality and morbidity are due to cell/tissue damage caused by replicative pressure and resource exhaustion, e.g., HBV or HIV; exaggerated immune responses, e.g., SARSCoV-2; and cancer, e.g., EBV or HPV. In this context, oncogenic and other types of viruses drive genetic and epigenetic changes that expand the tumorigenic program, including modifications to the ability of cancer cells to migrate. The best-characterized group of changes is collectively known as the epithelial–mesenchymal transition, or EMT. This is a complex phenomenon classically described using biochemistry, cell biology and genetics. However, these methods require enormous, often slow, efforts to identify and validate novel therapeutic targets. Systems biology can complement and accelerate discoveries in this field. One example of such an approach is Boolean networks, which make complex biological problems tractable by modeling data (“nodes”) connected by logical operators. Here, we focus on virus-induced cellular plasticity and cell reprogramming in mammals, and how Boolean networks could provide novel insights into the ability of some viruses to trigger uncontrolled cell proliferation and EMT, two key hallmarks of cancer.Universidad de Antioquia. Vicerrectoría de investigación. Comité para el Desarrollo de la Investigación - CODIColombia. 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