Cannabidiol directly targets mitochondria and disturbs calcium homeostasis in acute lymphoblastic leukemia

被引:101
作者
Olivas-Aguirre, Miguel [1 ]
Torres-Lopez, Liliana [1 ]
Salvador Valle-Reyes, Juan [1 ]
Hernandez-Cruz, Arturo [2 ,3 ]
Pottosin, Igor [1 ]
Dobrovinskaya, Oxana [1 ]
机构
[1] Univ Colima, Univ Ctr Biomed Res, Lab Immunobiol & Ion Transport Regulat, Ave 25 Julio 96, Colima 28030, Mexico
[2] Univ Nacl Autonoma Mexico, Inst Cellular Physiol, Dept Cognit Neurosci, Mexico City, DF, Mexico
[3] Univ Nacl Autonoma Mexico, Inst Cellular Physiol, Natl Lab Channelopathies LaNCa, Mexico City, DF, Mexico
关键词
MONITORING AUTOPHAGIC FLUX; CYTOCHROME-C RELEASE; PERMEABILITY TRANSITION; CELL-DEATH; MECHANISMS; RECEPTORS; APOPTOSIS; BINDS; CURE;
D O I
10.1038/s41419-019-2024-0
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Anticancer properties of non-psychoactive cannabinoid cannabidiol (CBD) have been demonstrated on tumors of different histogenesis. Different molecular targets for CBD were proposed, including cannabinoid receptors and some plasma membrane ion channels. Here we have shown that cell lines derived from acute lymphoblastic leukemia of T lineage (T-ALL), but not resting healthy T cells, are highly sensitive to CBD treatment. CBD effect does not depend on cannabinoid receptors or plasma membrane Ca2+-permeable channels. Instead, CBD directly targets mitochondria and alters their capacity to handle Ca2+. At lethal concentrations, CBD causes mitochondrial Ca2+ overload, stable mitochondrial transition pore formation and cell death. Our results suggest that CBD is an attractive candidate to be included into chemotherapeutic protocols for T-ALL treatment.
引用
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页数:19
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