Anti-leukemic effects of the V-ATPase inhibitor Archazolid A
Author(s) -
Siwei Zhang,
Lina S. Schneider,
Binje Vick,
M Grunert,
Irmela Jeremias,
Dirk Menche,
Rolf Müller,
Angelika M. Vollmar,
Johanna Liebl
Publication year - 2015
Publication title -
oncotarget
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.373
H-Index - 127
ISSN - 1949-2553
DOI - 10.18632/oncotarget.6180
Subject(s) - survivin , atpase , apoptosis , programmed cell death , cancer research , mechanism of action , cell culture , cell cycle , cell growth , pharmacology , medicine , microbiology and biotechnology , chemistry , biology , enzyme , biochemistry , in vitro , genetics
Prognosis for patients suffering from T-ALL is still very poor and new strategies for T-ALL treatment are urgently needed. Our study shows potent anti-leukemic effects of the myxobacterial V-ATPase inhibitor Archazolid A. Archazolid A reduced growth and potently induced death of leukemic cell lines and human leukemic samples. By inhibiting lysosomal acidification, Archazolid A blocked activation of the Notch pathway, however, this was not the mechanism of V-ATPase inhibition relevant for cell death induction. In fact, V-ATPase inhibition by Archazolid A decreased the anti-apoptotic protein survivin. As underlying mode of action, this work is in line with recent studies from our group demonstrating that Archazolid A induced S-phase cell cycle arrest by interfering with the iron metabolism in leukemic cells. Our study provides evidence for V-ATPase inhibition as a potential new therapeutic option for T-ALL.
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