TPEN induces apoptosis independently of zinc chelator activity in a model of acute lymphoblastic leukemia and ex vivo acute leukemia cells through oxidative stress and mitochondria caspase-3- and AIF-dependent pathways

ABSTRACT: Acute lymphoblastic leukemia is still an incurable disease with resistance to therapy developing in the majority of patients. We investigated the effect of TPEN, an intracellular zinc chelator, in Jurkat and in ex vivo acute lymphoblastic leukemia (ALL) cells resistant to chemotherapy. Cha...

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Autores:
Mendivil Pérez, Miguel Ángel
Jiménez del Río, Marlene
Vélez Pardo, Carlos Alberto
Tipo de recurso:
Article of investigation
Fecha de publicación:
2012
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/38546
Acceso en línea:
https://hdl.handle.net/10495/38546
Palabra clave:
Acetilcisteína - farmacología
Acetylcysteine - pharmacology
Apoptosis
Caspase 3
Núcleo Celular
Cell Nucleus
Relación Dosis-Respuesta a Droga
Dose-Response Relationship, Drug
Peróxido de Hidrógeno
Hydrogen Peroxide
Leucemia-Linfoma Linfoblástico de Células Precursoras
Precursor Cell Lymphoblastic Leukemia-Lymphoma
Potencial de la Membrana Mitocondrial - efectos de los fármacos
Membrane Potential, Mitochondrial - drug effects
Membrane Potential, Mitochondrial - drug effects
https://id.nlm.nih.gov/mesh/D000111
https://id.nlm.nih.gov/mesh/D017209
https://id.nlm.nih.gov/mesh/D053148
https://id.nlm.nih.gov/mesh/D002467
https://id.nlm.nih.gov/mesh/D004305
https://id.nlm.nih.gov/mesh/D006861
https://id.nlm.nih.gov/mesh/D054198
https://id.nlm.nih.gov/mesh/D053078
Rights
openAccess
License
https://creativecommons.org/licenses/by/4.0/
Description
Summary:ABSTRACT: Acute lymphoblastic leukemia is still an incurable disease with resistance to therapy developing in the majority of patients. We investigated the effect of TPEN, an intracellular zinc chelator, in Jurkat and in ex vivo acute lymphoblastic leukemia (ALL) cells resistant to chemotherapy. Changes of nuclei morphology, reactive oxygen species generation, presence of hypodiploid cells, phosphatidylserine translocation, mitochondrial membrane depolarization, immunohistochemical identification of cell death signalling molecules, and pharmacological inhibition were assayed to detect the apoptotic cell death pathways. We found that TPEN induces apoptosis in both types of cells by a molecular oxidative stress pathway involving O2->H2O2>> NF-κB (JNK/c-Jun) > p53 > m > loss caspase-3, AIF > chromatin condensation/DNA fragmentation. Interestingly, TPEN induced apoptosis independently of glucose; leukemic cells are therefore devoid of survival capacity by metabolic resistance to treatment. Most importantly, TPEN cytotoxic effect can eventually be regulated by the antioxidant N-acetyl-cysteine and zinc ions. Our data suggest that TPEN can be used as a potential therapeutic prooxidant agent against refractory leukemia. These data contribute to understanding the importance of oxidative stress in the treatment of ALL.