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Simulation study on electroporation of cancer cells in multicellular system.
Zhang, Yu; Luo, Zhijun; Zhang, Yapeng; Guo, Fei.
Afiliação
  • Zhang Y; Department of gynecology, Chongqing Traditional Chinese Medicine Hospital, Chongqing 400021, China. Electronic address: yuyu_xiaxia@163.com.
  • Luo Z; Institute of Ecological Safety, Chongqing University of Posts and Telecommunications, Chongqing 400065, China.
  • Zhang Y; Institute of Ecological Safety, Chongqing University of Posts and Telecommunications, Chongqing 400065, China.
  • Guo F; Institute of Ecological Safety, Chongqing University of Posts and Telecommunications, Chongqing 400065, China. Electronic address: guofei@cqupt.edu.cn.
Bioelectrochemistry ; 160: 108789, 2024 Dec.
Article em En | MEDLINE | ID: mdl-39128409
ABSTRACT
Electroporation (EP) of the normal cell and cancer cell both in single-cell and multicellular models was investigated by the meshed transport network method (MTNM) in this paper. The simulation results suggest that the cancer cell undergoes faster and more significant local EP than that of the corresponding normal cell induced by nanosecond pulsed electric fields (nsPEFs) both in single-cell and multicellular models. Furthermore, the results of the multicellular model indicate that there is a unidirectional neighboring effect in the multicellular model, meaning that cells at the center are affected and their pore formation is significantly reduced, but this effect is very weak for cells at the edges of the system. This means that the electric field selectively kills cells in different distribution locations. This work can provide guidance for the selection of parameters for the cancer cell EP process.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Eletroporação / Modelos Biológicos / Neoplasias Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Eletroporação / Modelos Biológicos / Neoplasias Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article