8-Gingerol regulates colorectal cancer cell proliferation and migration through the EGFR/STAT/ERK pathway

被引:38
作者
Hu, Su-Min [1 ]
Yao, Xu-Hui [2 ]
Hao, Yi-Hai [2 ]
Pan, Ai-Hua [1 ]
Zhou, Xing-Wang [1 ]
机构
[1] Sun Yat Sen Univ, Zhongshan Sch Med, 74 Zhongshan 2nd Rd, Guangzhou 510080, Guangdong, Peoples R China
[2] Guangdong Expt High Sch, Guangzhou 510080, Guangdong, Peoples R China
关键词
8-gingerol; epidermal growth factor receptor; colorectal cancer; proliferation; migration; GROWTH-FACTOR RECEPTOR; CYCLE ARREST; LUNG-CANCER; IN-VITRO; APOPTOSIS; EGFR; 6-SHOGAOL; BREAST; ACTIVATION; 6-GINGEROL;
D O I
10.3892/ijo.2019.4934
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
8-Gingerol, which is extracted from ginger (Zingiber officinale Roscoe), has been shown to possess antioxidant and anti-inflammatory properties. However, the antitumor effect of 8-gingerol has not been fully elucidated. The aim of the present study was to investigate the therapeutic potential of 8-gingerol against colorectal cancer (CRC). The results demonstrated that 8-gingerol significantly inhibited cell proliferation in CRC cell models. Treatment of CRC cells with 8-gingerol resulted in dose-dependent decreases in migration and invasion. The inhibitory effect of 8-gingerol on CRC cell growth was attributed to cell cycle arrest and increased apoptosis. Moreover, to the best of our knowledge, the present study was the first to demonstrate that 8-gingerol acted as an inhibitor of epidermal growth factor receptor (EGFR) signaling. 8-Gingerol inhibited CRC cell proliferation and migration by targeting the EGFR/signal transducer and activator of transcription/extracellular signal-regulated kinase pathway, and the effects of 8-gingerol depended on the expression of EGFR. Moreover, 8-gingerol reduced the effective dosage of 5-fluorouracil and, thereby, the toxicity of drug combination therapy. These data suggest that 8-gingerol may be a promising candidate for the development of novel anticancer agents against CRC.
引用
收藏
页码:390 / 397
页数:8
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