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Participation of suicide gene extracellular vesicles in metastasis prevention.
Vanova, Dajana; Andrezal, Michal; Jakubechova, Jana; Altanerova, Ursula; Altaner, Cestmir.
Afiliação
  • Vanova D; Stem Cell Preparation Department, St. Elisabeth Cancer Institute, Bratislava, Slovakia.
  • Andrezal M; Stem Cell Preparation Department, St. Elisabeth Cancer Institute, Bratislava, Slovakia.
  • Jakubechova J; Stem Cell Preparation Department, St. Elisabeth Cancer Institute, Bratislava, Slovakia.
  • Altanerova U; Stem Cell Preparation Department, St. Elisabeth Cancer Institute, Bratislava, Slovakia.
  • Altaner C; Stem Cell Preparation Department, St. Elisabeth Cancer Institute, Bratislava, Slovakia.
Neoplasma ; 71(2): 117-122, 2024 Apr.
Article em En | MEDLINE | ID: mdl-38766855
ABSTRACT
The incidence of distant metastases is associated with most cancer-related mortalities. Extracellular vesicles (EVs), secreted from tumors and cancer-associated fibroblasts, are involved in the metastatic process mediating their organotropism through their involvement in the pre-metastatic niche formation. We have been developing suicide gene therapy mediated by EVs secreted from mesenchymal stem/ stromal cells, tumor cells, and cancer-associated fibroblasts. Suicide gene EVs conjugated with prodrug are tumor tropic, penetrate tumor cells, and kill them by intracellular conversion of nontoxic prodrug to an efficient anti-cancer drug. Here, we discuss findings regarding the possibility of using suicide gene EVs as a novel therapeutic approach for metastases, via pre-metastatic niche modification. The suicide gene EVs provide a future perspective for metastasis prevention.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Genes Transgênicos Suicidas / Vesículas Extracelulares / Metástase Neoplásica Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Genes Transgênicos Suicidas / Vesículas Extracelulares / Metástase Neoplásica Idioma: En Ano de publicação: 2024 Tipo de documento: Article