Hypoxia potentiates the cytotoxic effect of piperlongumine in pheochromocytoma models

被引:11
作者
Bullova, Petra [1 ,2 ]
Cougnoux, Antony [3 ]
Abunimer, Luma [1 ]
Kopacek, Juraj [2 ]
Pastorekova, Silvia [2 ]
Pacak, Karel [1 ]
机构
[1] Eunice Kennedy Shriver NICHD, Sect Med Neuroendocrinol, NIH, Bethesda, MD 20892 USA
[2] Slovak Acad Sci, Dept Mol Med, Inst Virol, Biomed Res Ctr, Bratislava 84505, Slovakia
[3] Eunice Kennedy Shriver NICHD, Sect Mol Dysmorphol, NIH, Bethesda, MD 20892 USA
关键词
pheochromocytoma; piperlongumine; hypoxia; reactive-oxygen species; apoptosis; PROTEASOME INHIBITOR BORTEZOMIB; CANCER CELL-DEATH; MESENCHYMAL TRANSITION; APOPTOSIS; AUTOPHAGY; ACTIVATION; NECROPTOSIS; MECHANISMS; INDUCTION; ROS;
D O I
10.18632/oncotarget.9643
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hypoxia is a common feature of solid tumors that activates a plethora of pathways, resulting in proliferation and resistance of cancer cells to radio-and chemotherapy. Pheochromocytomas/paragangliomas (PHEOs/PGLs) with mutations in the gene coding for the subunit B of succinate dehydrogenase (SDHB) are the most aggressive forms of the disease, which is partially due to their pseudohypoxic character, metabolic abnormalities, and elevated reactive oxygen species (ROS) levels. We investigated the effect of piperlongumine (PL), a natural product with cytotoxic properties restricted to cancer cells by significantly increasing intracellular ROS levels, on PHEO cells. Here we report for the first time that PL mediates PHEO cell death by activating both apoptosis and necroptosis in vitro and in vivo. This effect is magnified in hypoxic conditions, making PL a promising potential candidate for use as a therapeutic option for patients with PHEO/PGL, including those with SDHB mutations.
引用
收藏
页码:40531 / 40545
页数:15
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