Chang Cheng-Yi, Li Jian-Ri, Wu Chih-Cheng, Ou Yen-Chuan, Chen Wen-Ying, Kuan Yu-Hsiang, Wang Wen-Yi, Chen Chun-Jung
Department of Surgery, Feng Yuan Hospital, Taichung, Taiwan.
Graduate Institute of Pharmaceutical Science and Technology, Central Taiwan University of Science and Technology, Taichung, Taiwan.
IUBMB Life. 2015 Nov;67(11):869-79. doi: 10.1002/iub.1445. Epub 2015 Oct 21.
Autophagy and apoptosis represent important cellular processes involved in cancer cell killing mechanisms. Epidermal growth factor receptor inhibitor gefitinib and valproic acid have been implicated in the treatment of malignancies including glioma involving autophagic and apoptotic mechanisms. Therefore, it is interesting to investigate whether a combination of gefitinib and valproic acid shows better cancer cell killing effect on human glioma cells. We found that a nontoxic concentration of valproic acid sensitized U87 and T98G glioma cells to gefitinib cytotoxicity by inhibiting cell growth and long-term clonogenic survival. The augmented consequences were accompanied by the formation of autophagic vacuoles, conversion of microtubule-associated protein-1 light chain 3-II (LC3-II), and degradation of p62. Autophagy inhibitor 3-methyladenosine and chloroquine and genetic silencing of LC3 but not broad-spectrum caspase inhibitor attenuated gefitinib/valproic acid-induced growth inhibition. Gefitinib/valproic acid-induced autophagy was accompanied by the activation of liver kinase-B1 (LKB1)/AMP-activated protein kinase (AMPK)/ULK1. Silencing of AMPK and ULK1 suppressed gefitinib/valproic acid-induced autophagy and growth inhibition. Mechanistic studies showed that gefitinib/valproic acid increased intracellular reactive oxygen species generation and N-acetyl cysteine attenuated gefitinib/valproic acid-caused autophagy and growth inhibition. In addition to demonstrating the autophagic mechanisms of gefitinib/valproic acid, the results of this study further suggest that intracellular oxidative stress and the LKB1/AMPK signaling might be a potential target for the development of therapeutic strategy against glioma.
自噬和凋亡是参与癌细胞杀伤机制的重要细胞过程。表皮生长因子受体抑制剂吉非替尼和丙戊酸已被用于治疗包括胶质瘤在内的恶性肿瘤,其涉及自噬和凋亡机制。因此,研究吉非替尼和丙戊酸联合使用是否对人胶质瘤细胞具有更好的癌细胞杀伤效果很有意义。我们发现,无毒浓度的丙戊酸通过抑制细胞生长和长期克隆存活,使U87和T98G胶质瘤细胞对吉非替尼的细胞毒性敏感。增强的结果伴随着自噬空泡的形成、微管相关蛋白1轻链3-II(LC3-II)的转化以及p62的降解。自噬抑制剂3-甲基腺嘌呤和氯喹以及LC3的基因沉默,但不是广谱半胱天冬酶抑制剂,减弱了吉非替尼/丙戊酸诱导的生长抑制。吉非替尼/丙戊酸诱导的自噬伴随着肝激酶-B1(LKB1)/AMP激活蛋白激酶(AMPK)/ULK1的激活。AMPK和ULK1的沉默抑制了吉非替尼/丙戊酸诱导的自噬和生长抑制。机制研究表明,吉非替尼/丙戊酸增加细胞内活性氧的产生,N-乙酰半胱氨酸减弱吉非替尼/丙戊酸引起的自噬和生长抑制。除了证明吉非替尼/丙戊酸的自噬机制外,本研究结果进一步表明,细胞内氧化应激和LKB1/AMPK信号可能是开发抗胶质瘤治疗策略的潜在靶点。