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Circulating cells and exosomes in acute myelogenous leukemia and their role in disease progression and survival.
Miyamoto, Kendi Nishino; Bonatto, Diego.
Afiliação
  • Miyamoto KN; Centro de Biotecnologia, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.. Electronic address: kendinm@gmail.com.
  • Bonatto D; Centro de Biotecnologia, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Clin Immunol ; 217: 108489, 2020 08.
Article em En | MEDLINE | ID: mdl-32492479
ABSTRACT
Acute myelogenous leukemia (AML) is an aggressive hematological malignancy associated with high rates of mortality. This incidence is due to the complexity in which the AML cells interact with other healthy human cells. These phenomena create an environment that favors the expansion of leukemic cells, which will affect the patient's prognosis. An important aspect is the ability of AML cells to evade immune responses via targeting and signaling immune cells to suppress anti-tumor responses. Many studies have reported that associations among components in the peripheral bloodstream might modulate leukemic progression because AML survival is a fundamental step for recolonizing bone marrow after allogeneic hematopoietic stem cell (HSC) transplantation or chemotherapy. Therefore, we collected the most important data about components that circulate with leukemic blasts and contribute to their survival and proliferation. We also discuss clinical approaches that could be conducted to more effectively treat the disease.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células-Tronco / Células Dendríticas / Células Matadoras Naturais / Leucemia Mieloide Aguda / Linfócitos T Reguladores / Células Endoteliais / Exossomos Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células-Tronco / Células Dendríticas / Células Matadoras Naturais / Leucemia Mieloide Aguda / Linfócitos T Reguladores / Células Endoteliais / Exossomos Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article