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Induction of hypoxia-inducible factor-1alpha inhibits drug-induced apoptosis in the human leukemic cell line HL-60
Korean Journal of Hematology ; : 158-163, 2010.
Artigo em Inglês | WPRIM | ID: wpr-720398
ABSTRACT

BACKGROUND:

Leukemic cells originate from hypoxic bone marrow, which protects them from anti-cancer drugs. Although many factors that cause drug resistance in leukemic cells have been studied, the effect of hypoxia on drug-induced apoptosis is still poorly understood.

METHODS:

In this study, we examined the effect of hypoxia on anti-leukemic drug resistance in leukemic cell lines treated with cobalt chloride (CoCl2), a hypoxia-mimetic agent. Cellular proliferation was evaluated using the methyl thiazolyl tetrazolium (MTT) assay. Flow cytometry analysis and western blots were performed to investigate apoptosis-related proteins.

RESULTS:

Unlike its previously known apoptotic effect, the expression of HIF-1alpha increased the survival rate of human promyelocytic leukemia HL-60 cells when these cells were exposed to anti-leukemic drugs; these effects were mediated by heat-shock protein HSP70 and the pro-apoptotic protein Bax.

CONCLUSION:

These findings may provide new insights for understanding the mechanisms underlying hypoxia and for designing new therapeutic strategies for acute myeloid leukemia.
Assuntos

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Óxidos / Arsenicais / Medula Óssea / Resistência a Medicamentos / Leucemia Mieloide Aguda / Leucemia / Proteínas / Linhagem Celular / Western Blotting / Taxa de Sobrevida Limite: Humanos Idioma: Inglês Revista: Korean Journal of Hematology Ano de publicação: 2010 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Óxidos / Arsenicais / Medula Óssea / Resistência a Medicamentos / Leucemia Mieloide Aguda / Leucemia / Proteínas / Linhagem Celular / Western Blotting / Taxa de Sobrevida Limite: Humanos Idioma: Inglês Revista: Korean Journal of Hematology Ano de publicação: 2010 Tipo de documento: Artigo