Lysosomal membrane permeabilization is involved in curcumin-induced apoptosis of A549 lung carcinoma cells

被引:49
作者
Chen, Qing-Yong [1 ]
Shi, Jian-Guo [1 ]
Yao, Qing-Hua [2 ]
Jiao, De-Min [1 ]
Wang, Yan-Yi [3 ]
Hu, Hui-Zhen [1 ]
Wu, Yu-Quan [1 ]
Song, Jia [1 ]
Yan, Jie [1 ]
Wu, Li-Jun [1 ]
机构
[1] 117th Hosp PLA, Dept Resp Dis, Hangzhou 310013, Zhejiang, Peoples R China
[2] Med Univ, Dept Resp Dis, Affiliated Hosp 1, Hangzhou 310003, Zhejiang, Peoples R China
[3] Guizhou Univ, Coll Life Sci, Guiyang 550025, Peoples R China
关键词
Curcumin; Apoptosis; Reactive oxygen species; Lung cancer; Lysosomal membrane permeabilization; TUMOR-NECROSIS-FACTOR; HEPATOMA G2 CELLS; NF-KAPPA-B; OXIDATIVE STRESS; DEATH; MITOCHONDRIAL; DISRUPTION; ACTIVATION; PATHWAYS; KINASE;
D O I
10.1007/s11010-011-1033-9
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We previously reported that curcumin inhibited lung cancer A549 cells growth and promoted cell apoptosis in vitro. In this study, we further examined the apoptosis-related parameters, including lysosomal damage and cathepsin activation, in A549 cells exposed to curcumin. We found that curcumin caused lysosomal membrane permeabilization (LMP) and cytosolic relocation of cathepsin B (cath B) and cathepsin D (cath D). However, only Z-FA-fmk (a cath B inhibitor) but not pepstatin A (a cath D inhibitor) inhibited curcumin-induced cell apoptosis, mitochondrial membrane potential loss, and cytochrome c release. The antioxidant N-acetylcysteine and glutathione attenuated LMP, suggesting that lysosomal destabilization was dependent on the elevation of reactive oxygen species and which precedes mitochondrial dysfunction. These findings indicated a novel pathway for curcumin regulation of ROS-lysosomal-mitochondrial pathway and provided the key mechanism of regulation of LMP in cell apoptosis, which may be exploited for cancer treatment.
引用
收藏
页码:389 / 398
页数:10
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