GSK1059615 kills head and neck squamous cell carcinoma cells possibly via activating mitochondrial programmed necrosis pathway

被引:42
作者
Xie, Jing [1 ]
Li, Quan [2 ]
Ding, Xi [1 ]
Gao, Yunyun [1 ]
机构
[1] Wenzhou Med Univ, Affiliated Hosp 1, Dept Stomatol, Wenzhou, Peoples R China
[2] Soochow Univ, Affiliated Hosp 2, Ctr Stomatol, Suzhou, Peoples R China
关键词
HNSCC; PI3K-AKT-mTOR; GSK1059615; programmed necrosis; PERMEABILITY TRANSITION PORE; MOLECULAR TARGETED THERAPIES; COLORECTAL-CANCER CELLS; NON-APOPTOTIC DEATH; CYCLOPHILIN-D; IN-VITRO; AKT INHIBITOR; GROWTH; VIVO; OSTEOBLASTS;
D O I
10.18632/oncotarget.15135
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
This study tested the anti-head and neck squamous cell carcinoma (HNSCC) cell activity by GSK1059615, a novel PI3K and mTOR dual inhibitor. GSK1059615 inhibited survival and proliferation of established (SCC-9, SQ20B and A253 lines) and primary human HNSCC cells. GSK1059615 blocked PI3K-AKT-mTOR activation in HNSCC cells. Intriguingly, GSK1059615 treatment in HNSCC cells failed to provoke apoptosis, but induced programmed necrosis. The latter was tested by mitochondria depolarization, ANT-1-cyclophilin-D mitochondrial association and lactate dehydrogenase (LDH) release. Reversely, mPTP blockers (sanglifehrin A, cyclosporin A and bongkrekic acid) or cyclophilin-D shRNA dramatically alleviated GSK1059615-induced SCC-9 cell death. Further studies demonstrated that GSK1059615 i.p. injection suppressed SCC-9 tumor growth in nude mice, which was compromised with co-administration with cyclosporin A. Thus, targeting PI3K-AKT-mTOR pathway by GSK1059615 possibly provokes programmed necrosis pathway to kill HNSCC cells.
引用
收藏
页码:50814 / 50823
页数:10
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