Nalazite se na CroRIS probnoj okolini. Ovdje evidentirani podaci neće biti pohranjeni u Informacijskom sustavu znanosti RH. Ako je ovo greška, CroRIS produkcijskoj okolini moguće je pristupi putem poveznice www.croris.hr
izvor podataka: crosbi

AICAR induces differentiation of acute myeloid leukemia cells (CROSBI ID 201357)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Lalić, Hrvoje ; Dembitz, Vilma ; Lukinović-Škudar, Vesna ; Banfić, Hrvoje ; Višnjić, Dora AICAR induces differentiation of acute myeloid leukemia cells // Leukemia & lymphoma, 55 (2014), 10; 2375-2383. doi: 10.3109/10428194.2013.876633

Podaci o odgovornosti

Lalić, Hrvoje ; Dembitz, Vilma ; Lukinović-Škudar, Vesna ; Banfić, Hrvoje ; Višnjić, Dora

engleski

AICAR induces differentiation of acute myeloid leukemia cells

AMP-activated kinase (AMPK) modulators have been shown to exert cytotoxic activity in hematological malignancies, but their role in differentiation of acute myeloid leukemia (AML) is less explored. In this study, the effects of AMPK agonists on all- trans retinoic acid (ATRA)-mediated differentiation of acute promyelocytic leukemia (APL) and non-APL AML cell lines were investigated. The results show that APMK agonists inhibit growth of myeloblastic HL-60, promyelocytic NB4 and monocytic U937 cells. 5- aminoimidazole-4-carboxamide ribonucleoside (AICAR), an AMPK activator, enhances ATRA-mediated differentiation of NB4 cells. In U937 cells, AICAR alone induces the expression of cell surface markers associated with mature monocytes and macrophages. In both cell lines, AICAR increases the activity of mitogen-activated protein kinase (MAPK), and the presence of a MAPK inhibitor reduces the expression of differentiation markers. These results revealed beneficial effects of AICAR in AML, including differentiation of non-APL AML cells.

AICAR; differentiation markers; leukemia

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

Podaci o izdanju

55 (10)

2014.

2375-2383

objavljeno

1042-8194

10.3109/10428194.2013.876633

Povezanost rada

Temeljne medicinske znanosti

Poveznice
Indeksiranost