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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Effect of cortisol on K562 leukemia cells

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Autor(es):
Fonseca, Marcelo de Oliveira [1] ; da Silva, Newton Soares [1] ; Soares, Cristina Pacheco [1]
Número total de Autores: 3
Afiliação do(s) autor(es):
[1] Univ Vale Paraiba, Sao Paulo, SP - Brazil
Número total de Afiliações: 1
Tipo de documento: Artigo Científico
Fonte: Revista O Mundo da Saúde; v. 43, n. 4, p. 854-861, OCT-DEC 2019.
Citações Web of Science: 0
Resumo

Numerous studies describe effects caused by stress on the development, progression and poor prognosis of various pathologies, such as cancer. In recent decades, researchers have investigated the role of stress-associated hormones and cancer progression. Cortisol is described as a primary stress hormone in the human body. Studies show a positive correlation of elevated cortisol levels and cancer progression. Increased cell proliferation and increased reactive oxygen species that contribute to DNA damage, dysplasia, and neoplasms are the result of prolonged stress where tissue becomes insensitive to cortisol, the primary human stress hormone. This study explores the influence of cortisol, an important hormone involved in stress, on tumor cell development, particularly in human cells of chronic myeloid leukemia (K562). K562 cells were exposed to increasing cortisol (hydrocortisone) concentrations for 24 or 48 hours and cytotoxicity (MIT assay 13-(4,5-dimethylthiazolyl-2)-2,5-diphenyltetrazio bromide] and cell death processes (fluorescence microscopy) were investigated. Our data show a considerable role of cortisol not only in mitochondrial activity, but also in the processes of proliferation and apoptotic and necrotic death in K562 cells. These results demonstrate the possible influence of stress on tumor development and demonstrate that K562 cells can be adapted to cortisol levels over time. (AU)

Processo FAPESP: 16/17984-1 - Avaliação de glicanos, proteínas de choque térmico e fagocitose após tratamento fotodinâmica.
Beneficiário:Cristina Pacheco Soares
Modalidade de apoio: Auxílio à Pesquisa - Regular
Processo FAPESP: 09/15206-8 - Mecanismos celulares da inativação tumoral através da terapia fotodinâmica
Beneficiário:Cristina Pacheco Soares
Modalidade de apoio: Auxílio à Pesquisa - Regular