A multiscale cell-based model of tumor growth for chemotherapy assessment and tumor-targeted therapy through a 3D computational approach
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
DOI: | 10.1111/cpr.13187 |
Texto Completo: | http://hdl.handle.net/10316/103214 https://doi.org/10.1111/cpr.13187 |
Resumo: | Objectives: Computational modeling of biological systems is a powerful tool to clarify diverse processes contributing to cancer. The aim is to clarify the complex biochemical and mechanical interactions between cells, the relevance of intracellular signaling pathways in tumor progression and related events to the cancer treatments, which are largely ignored in previous studies. Materials and Methods: A three-dimensional multiscale cell-based model is developed, covering multiple time and spatial scales, including intracellular, cellular, and extracellular processes. The model generates a realistic representation of the processes involved from an implementation of the signaling transduction network. Results: Considering a benign tumor development, results are in good agreement with the experimental ones, which identify three different phases in tumor growth. Simulating tumor vascular growth, results predict a highly vascularized tumor morphology in a lobulated form, a consequence of cells' motile behavior. A novel systematic study of chemotherapy intervention, in combination with targeted therapy, is presented to address the capability of the model to evaluate typical clinical protocols. The model also performs a dose comparison study in order to optimize treatment efficacy and surveys the effect of chemotherapy initiation delays and different regimens. Conclusions: Results not only provide detailed insights into tumor progression, but also support suggestions for clinical implementation. This is a major step toward the goal of predicting the effects of not only traditional chemotherapy but also tumor-targeted therapies. |
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A multiscale cell-based model of tumor growth for chemotherapy assessment and tumor-targeted therapy through a 3D computational approachcellular Potts modelchemotherapycomputational biologysignaling transductiontargeted therapytumor-induced angiogenesisCell ProliferationHumansModels, BiologicalNeoplasmsNeovascularization, PathologicSignal TransductionComputer SimulationObjectives: Computational modeling of biological systems is a powerful tool to clarify diverse processes contributing to cancer. The aim is to clarify the complex biochemical and mechanical interactions between cells, the relevance of intracellular signaling pathways in tumor progression and related events to the cancer treatments, which are largely ignored in previous studies. Materials and Methods: A three-dimensional multiscale cell-based model is developed, covering multiple time and spatial scales, including intracellular, cellular, and extracellular processes. The model generates a realistic representation of the processes involved from an implementation of the signaling transduction network. Results: Considering a benign tumor development, results are in good agreement with the experimental ones, which identify three different phases in tumor growth. Simulating tumor vascular growth, results predict a highly vascularized tumor morphology in a lobulated form, a consequence of cells' motile behavior. A novel systematic study of chemotherapy intervention, in combination with targeted therapy, is presented to address the capability of the model to evaluate typical clinical protocols. The model also performs a dose comparison study in order to optimize treatment efficacy and surveys the effect of chemotherapy initiation delays and different regimens. Conclusions: Results not only provide detailed insights into tumor progression, but also support suggestions for clinical implementation. This is a major step toward the goal of predicting the effects of not only traditional chemotherapy but also tumor-targeted therapies.2022-03info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/103214http://hdl.handle.net/10316/103214https://doi.org/10.1111/cpr.13187eng0960-77221365-2184Jafari Nivlouei, SaharSoltani, MadjidShirani, EbrahimSalimpour, Mohammad RezaTravasso, Rui D.Carvalho, Joãoinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2022-10-24T20:32:48Zoai:estudogeral.uc.pt:10316/103214Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:20:05.277459Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
A multiscale cell-based model of tumor growth for chemotherapy assessment and tumor-targeted therapy through a 3D computational approach |
title |
A multiscale cell-based model of tumor growth for chemotherapy assessment and tumor-targeted therapy through a 3D computational approach |
spellingShingle |
A multiscale cell-based model of tumor growth for chemotherapy assessment and tumor-targeted therapy through a 3D computational approach A multiscale cell-based model of tumor growth for chemotherapy assessment and tumor-targeted therapy through a 3D computational approach Jafari Nivlouei, Sahar cellular Potts model chemotherapy computational biology signaling transduction targeted therapy tumor-induced angiogenesis Cell Proliferation Humans Models, Biological Neoplasms Neovascularization, Pathologic Signal Transduction Computer Simulation Jafari Nivlouei, Sahar cellular Potts model chemotherapy computational biology signaling transduction targeted therapy tumor-induced angiogenesis Cell Proliferation Humans Models, Biological Neoplasms Neovascularization, Pathologic Signal Transduction Computer Simulation |
title_short |
A multiscale cell-based model of tumor growth for chemotherapy assessment and tumor-targeted therapy through a 3D computational approach |
title_full |
A multiscale cell-based model of tumor growth for chemotherapy assessment and tumor-targeted therapy through a 3D computational approach |
title_fullStr |
A multiscale cell-based model of tumor growth for chemotherapy assessment and tumor-targeted therapy through a 3D computational approach A multiscale cell-based model of tumor growth for chemotherapy assessment and tumor-targeted therapy through a 3D computational approach |
title_full_unstemmed |
A multiscale cell-based model of tumor growth for chemotherapy assessment and tumor-targeted therapy through a 3D computational approach A multiscale cell-based model of tumor growth for chemotherapy assessment and tumor-targeted therapy through a 3D computational approach |
title_sort |
A multiscale cell-based model of tumor growth for chemotherapy assessment and tumor-targeted therapy through a 3D computational approach |
author |
Jafari Nivlouei, Sahar |
author_facet |
Jafari Nivlouei, Sahar Jafari Nivlouei, Sahar Soltani, Madjid Shirani, Ebrahim Salimpour, Mohammad Reza Travasso, Rui D. Carvalho, João Soltani, Madjid Shirani, Ebrahim Salimpour, Mohammad Reza Travasso, Rui D. Carvalho, João |
author_role |
author |
author2 |
Soltani, Madjid Shirani, Ebrahim Salimpour, Mohammad Reza Travasso, Rui D. Carvalho, João |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Jafari Nivlouei, Sahar Soltani, Madjid Shirani, Ebrahim Salimpour, Mohammad Reza Travasso, Rui D. Carvalho, João |
dc.subject.por.fl_str_mv |
cellular Potts model chemotherapy computational biology signaling transduction targeted therapy tumor-induced angiogenesis Cell Proliferation Humans Models, Biological Neoplasms Neovascularization, Pathologic Signal Transduction Computer Simulation |
topic |
cellular Potts model chemotherapy computational biology signaling transduction targeted therapy tumor-induced angiogenesis Cell Proliferation Humans Models, Biological Neoplasms Neovascularization, Pathologic Signal Transduction Computer Simulation |
description |
Objectives: Computational modeling of biological systems is a powerful tool to clarify diverse processes contributing to cancer. The aim is to clarify the complex biochemical and mechanical interactions between cells, the relevance of intracellular signaling pathways in tumor progression and related events to the cancer treatments, which are largely ignored in previous studies. Materials and Methods: A three-dimensional multiscale cell-based model is developed, covering multiple time and spatial scales, including intracellular, cellular, and extracellular processes. The model generates a realistic representation of the processes involved from an implementation of the signaling transduction network. Results: Considering a benign tumor development, results are in good agreement with the experimental ones, which identify three different phases in tumor growth. Simulating tumor vascular growth, results predict a highly vascularized tumor morphology in a lobulated form, a consequence of cells' motile behavior. A novel systematic study of chemotherapy intervention, in combination with targeted therapy, is presented to address the capability of the model to evaluate typical clinical protocols. The model also performs a dose comparison study in order to optimize treatment efficacy and surveys the effect of chemotherapy initiation delays and different regimens. Conclusions: Results not only provide detailed insights into tumor progression, but also support suggestions for clinical implementation. This is a major step toward the goal of predicting the effects of not only traditional chemotherapy but also tumor-targeted therapies. |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022-03 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10316/103214 http://hdl.handle.net/10316/103214 https://doi.org/10.1111/cpr.13187 |
url |
http://hdl.handle.net/10316/103214 https://doi.org/10.1111/cpr.13187 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
0960-7722 1365-2184 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
instname_str |
Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
repository.mail.fl_str_mv |
|
_version_ |
1822183293502619648 |
dc.identifier.doi.none.fl_str_mv |
10.1111/cpr.13187 |