Molecular Pathways Leading to Induction of Cell Death and Anti-Proliferative Properties by Tacrolimus and mTOR Inhibitors in Liver Cancer Cells

[Background/Aims] Orthotopic liver transplantation (OLT) is the recommended treatment for patients at early stages of hepatocarcinoma (HCC) with portal hypertension and/or increased bilirubinemia, but without vascular-associated diseases. Tumor recurrence, which is the main drawback for the survival...

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Detalhes bibliográficos
Autores: Navarro-Villarán, Elena, Cruz, Patricia de la, Contreras, Laura, González, Raúl, Negrete, María, Rodríguez-Hernández, María A., Marín-Gómez, Luis M., Álamo-Martinez, José M., Calvo, Antonio, Gómez-Bravo, Miguel A., Cruz, Jesús de la, Padillo-Ruíz, Javier, Muntané, Jordi
Formato: artículo
Estado:Versión publicada
Fecha de publicación:2020
País:España
Recursos:Consejo Superior de Investigaciones Científicas (CSIC)
Repositorio:DIGITAL.CSIC. Repositorio Institucional del CSIC
OAI Identifier:oai:digital.csic.es:10261/235717
Acesso em linha:http://hdl.handle.net/10261/235717
Access Level:acceso abierto
Palavra-chave:Apoptosis
Autophagy
Endoplasmic reticulum stress
Immunosuppressants
Hepatocarcinoma
Descrição
Resumo:[Background/Aims] Orthotopic liver transplantation (OLT) is the recommended treatment for patients at early stages of hepatocarcinoma (HCC) with portal hypertension and/or increased bilirubinemia, but without vascular-associated diseases. Tumor recurrence, which is the main drawback for the survival of patients submitted to OLT for HCC, has been related to tumor-related variables and the immunosuppressive therapies. We have previously shown that Tacrolimus (FK506) exerts a more potent pro-apoptotic and anti-proliferative effects than the mammalian target of rapamycin (mTOR) inhibitors (Sirolimus and Everolimus) in liver cancer cells. This study identified the role of the immunosuppressant partners such as FK506-binding proteins (FKBPs) in the induction of cell death and arrest of cell proliferation by immunosuppressants in two representative liver cancer cells.