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漆树酸诱导细胞凋亡与诱导 ATF4 依赖性内质网应激有关。

Anacardic acid induces cell apoptosis associated with induction of ATF4-dependent endoplasmic reticulum stress.

机构信息

State Key Lab of Respiratory Disease, Protein Modification and Degradation Lab, Department of Pathophysiology, Guangzhou Medical University, Guangdong 510182, People's Republic of China.

State Key Lab of Respiratory Disease, Protein Modification and Degradation Lab, Department of Pathophysiology, Guangzhou Medical University, Guangdong 510182, People's Republic of China; Guangzhou Research Institute of Cardiovascular Disease, The Second Affiliated Hospital, Guangzhou Medical University, Guangzhou, Guangdong 510260, People's Republic of China.

出版信息

Toxicol Lett. 2014 Aug 4;228(3):170-8. doi: 10.1016/j.toxlet.2014.05.012. Epub 2014 May 20.

Abstract

Anacardic acid (6-pentadecylsalicylic acid, AA), a natural compound isolated from the traditional medicine Amphipterygium adstringens, has been reported to possess antitumor activities. However, its molecular targets have not been thoroughly studied. Here, we report that AA is a potent inducer of endoplasmic reticulum (ER) stress, leading to apoptosis in hepatoma HepG2 and myeloma U266 cells. Induction of ER stress by AA was supported by a dose- and time-dependent increase in expression of the ER signaling downstream molecules, such as GRP78/BiP, phosphorylated eIF2α, ATF4 and CHOP in both HepG2 and U266 cell lines. Blockage of ATF4 expression by siRNA partially inhibited, while knockdown of CHOP expression by siRNA slightly increased AA-induced cell death in these cells. In addition, AA suppressed HepG2 xenograft tumor growth, associated with increased ER stress in vivo. These results suggest that AA induces tumor cell apoptosis associated with ATF4-dependent ER stress.

摘要

漆树酸(6-十五烷基水杨酸,AA)是一种从传统药物 Amphipterygium adstringens 中分离得到的天然化合物,据报道具有抗肿瘤活性。然而,其分子靶点尚未得到深入研究。在这里,我们报告 AA 是内质网(ER)应激的有效诱导剂,导致肝癌 HepG2 和骨髓瘤 U266 细胞凋亡。AA 诱导的 ER 应激得到了支持,其表现为 HepG2 和 U266 细胞系中 ER 信号下游分子如 GRP78/BiP、磷酸化 eIF2α、ATF4 和 CHOP 的表达呈剂量和时间依赖性增加。siRNA 阻断 ATF4 的表达部分抑制,而 siRNA 下调 CHOP 的表达则略微增加 AA 诱导的这些细胞中的细胞死亡。此外,AA 抑制 HepG2 异种移植肿瘤生长,与体内 ER 应激增加相关。这些结果表明,AA 诱导肿瘤细胞凋亡与 ATF4 依赖性 ER 应激有关。

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