β-elemene regulates endoplasmic reticulum stress to induce the apoptosis of NSCLC cells through PERK/IRE1α/ATF6 pathway

被引:61
作者
Liu, Ying [1 ,2 ]
Jiang, Zi-yu [1 ,3 ]
Zhou, Yuan-li [1 ]
Qiu, Hui-hui [1 ,3 ]
Wang, Gang [1 ,2 ]
Luo, Yi [1 ,3 ]
Liu, Jing-bing [1 ,3 ]
Liu, Xiong-wei [4 ]
Bu, Wei-quan [1 ,3 ]
Song, Jie [1 ,3 ]
Cui, Li [1 ,3 ]
Jia, Xiao-bin [1 ,3 ]
Feng, Liang [1 ,3 ]
机构
[1] Jiangsu Prov Acad Chinese Med, Key Lab New Drug Delivery Syst Chinese Mat Med, Nanjing 210028, Jiangsu, Peoples R China
[2] Anhui Univ Chinese Med, Sch Pharm, Hefei 230038, Anhui, Peoples R China
[3] Nanjing Univ Chinese Med, Sch Clin Med 3, Nanjing 210028, Jiangsu, Peoples R China
[4] Southeast Univ Med Collage, Affiliated Jiangyin Hosp, Jiangyin 214400, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
beta-elemene; Non-small-cell lung cancer; Endoplasmic reticulum stress; Apoptosis; UNFOLDED PROTEIN RESPONSE; LUNG-CARCINOMA CELLS; GLIOBLASTOMA CELLS; TUMOR-CELLS; SIGNALING PATHWAY; DOWN-REGULATION; CANCER CELLS; ER STRESS; IN-VITRO; ACTIVATION;
D O I
10.1016/j.biopha.2017.06.073
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Endoplasmic reticulum stress (ERs) has been regarded as an important cause for the pathogenesis of non-small-cell lung cancer (NSCLC). beta-elemene is an active component in the essential oil extracted from a medicinal herb, Curcuma wenyujin, and has been reported to be effective against non-small-cell lung cancer (NSCLC). However, the potential effect and underlying mechanisms of beta-elemene on regulating ERs to inhibit NSCLC are still unclear. In the present study, A549 cells and Lewis tumor-bearing C57BL/6J mice were established to evaluate this effect. Visualsonics Vevo 2100 Small Animal Dedicated High-frequency Color Ultrasound was performed to observe tumor volume in vivo. 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) was used to evaluate cell vitality of A549 cells. Furthermore, western blotting (WB), immunohistochemistry (IHC) and quantitative reverse transcription polymerase chain reaction (q-PCR) were applied to detect the ERs-related proteins. Flow cytometry was also applied to detect cell apoptosis and assay kit for reactive oxygen species (ROS) generation. Our results showed that beta-elemene inhibited lung cancer tumor growth and cell vitality in a dose-and time-dependent manner. Not only that, beta-elemene could up-regulate ERs-related proteins like PERK, IRE1 alpha, ATF6, ATF4, CHOP and down-regulate the Bcl-2 expression. More importantly, ERs inhibitor 4-PBA, IRE1 alpha inhibitor STF-083010, ATF6 inhibitor Anti-ATF6 and PERK inhibitor GSK2656157 can all reduce the amplitude of protein expression changes and apoptosis rates, then weaken the anti-tumor effect of beta-elemene. Therefore, the present in vivo and in vitro study revealed that the anti-NSCLC effect of beta-elemene is closely related to the activation of ERs through PERK/IRE1 alpha/ATF6 pathway, and this might be beneficial for clinical therapy of NSCLC. (C) 2017 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:490 / 497
页数:8
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