Autor: |
Lomovskaya, Ya. V., Kobyakova, M. I., Senotov, A. S., Fadeeva, I. S., Lomovsky, A. I., Krasnov, K. S., Shtatnova, D. Yu., Akatov, V. S., Fadeev, R. S. |
Zdroj: |
Biochemistry (Biokhimiya). Supplemental Series A, Membrane & Cell Biology; Mar2023, Vol. 17 Issue 1, p43-57, 15p |
Abstrakt: |
The study of the mechanisms of resistance of tumor cells to TRAIL-induced death remains an urgent task since this cytokine is an important highly selective molecular effector of antitumor immunity. Our study showed that human leukemia cells THP-1, HL-60, and K562 increased their resistance to TRAIL-induced death in vitro as a result of induction of myeloid differentiation in them by exogenous factors in all directions of myelopoiesis, except for erythroid, by reducing the expression of DR4 and DR5 receptors on the cell surface. It was also found that ONC 201, tunicamycin, and SAHA (hydroxamic acid suberoylanilide), capable of causing an increase in the expression of DR5 in leukemic cells, suppressed their TRAIL resistance induced by differentiation factors. The results obtained are of interest for the development of drugs and strategies to improve the effectiveness of the treatment of myeloid leukemia. [ABSTRACT FROM AUTHOR] |
Databáze: |
Complementary Index |
Externí odkaz: |
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