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...
- 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
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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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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 |
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https://id.nlm.nih.gov/mesh/D014780 |
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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 |
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2025-03-09T12:40:39Z |
| dc.date.available.none.fl_str_mv |
2025-03-09T12:40:39Z |
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Artículo de revisión |
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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. |
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https://hdl.handle.net/10495/45426 |
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10.3390/cells10112863 |
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2073-4409 |
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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 |
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https://hdl.handle.net/10495/45426 |
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eng |
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eng |
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Cells |
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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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