Rosmarinic acid reverses non-small cell lung cancer cisplatin resistance by activating the MAPK signaling pathway

被引:60
作者
Liao, Xiao-Zhong [1 ,2 ]
Gao, Ying [2 ]
Sun, Ling-Ling [1 ]
Liu, Jia-Hui [2 ]
Chen, Han-Rui [1 ]
Yu, Ling [1 ]
Chen, Zhuang-Zhong [1 ]
Chen, Wen-Hui [3 ]
Lin, Li-Zhu [1 ]
机构
[1] Guangzhou Univ Chinese Med, Affiliated Hosp 1, Dept Oncol, Yard 16,Airport Rd, Guangzhou 510405, Peoples R China
[2] Sun Yat Sen Univ, Affiliated Hosp 1, Dept Oncol, Guangzhou, Peoples R China
[3] Jinan Univ, Affiliated Hosp 1, Dept Oncol, Guangzhou 510630, Peoples R China
基金
中国国家自然科学基金;
关键词
cisplatin; MAPK; multidrug resistance; non-small cell lung cancer; rosmarinic acid; MULTIDRUG-RESISTANCE; ABC TRANSPORTERS; IN-VITRO; MECHANISMS; INHIBITORS; CARCINOMA; APOPTOSIS; EXTRACT; NSCLC;
D O I
10.1002/ptr.6584
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Cisplatin (DDP) is one of the first-line chemotherapeutic agents for non-small cell lung cancer (NSCLC). However, repeated use of cisplatin in clinical practice often induces chemoresistance. The aims of this study were to investigate whether rosmarinic acid (RA) could reverse multidrug resistance (MDR) in NSCLC and to explore the underlying mechanisms. Our data demonstrated that RA significantly inhibited NSCLC cell proliferation and cell colony formation in a dose-dependent manner, induced G1 phase cell cycle arrest and apoptosis, and increased the sensitivity of cell lines resistant to DDP. Mechanistically, RA inhibited NSCLC cell growth, arrested cell cycle, and induced apoptosis by activating MAPK and inhibiting the expression of P-gp and MDR1, which correspondingly enhanced p21 and p53 expression. We observed that the growth of xenograft tumors derived from NSCLC cell lines in nude mice was significantly inhibited by combination therapy. We demonstrate that RA is a potentially effective MDR reversal agent for NSCLC, based on downregulation of MDR1 mRNA expression and P-gp. Together, these results emphasize the putative role of RA as a resistance reversal agent in NSCLC.
引用
收藏
页码:1142 / 1153
页数:12
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