1. p-MEK expression predicts prognosis of patients with adenocarcinoma of esophagogastric junction (AEG) and plays a role in anti-AEG efficacy of Huaier
- Author
-
Shaowei Mo, Gui-Ping Chen, Zhiyuan Xu, Li Yuan, Wang Xiaofeng, Hang Lv, Jing-Li Xu, Kai-Bo Guo, Xiang-Dong Cheng, Can Hu, and Jiang-Jiang Qin
- Subjects
0301 basic medicine ,Male ,Esophageal Neoplasms ,MAP Kinase Signaling System ,Antineoplastic Agents ,Adenocarcinoma ,Complex Mixtures ,Pathogenesis ,03 medical and health sciences ,0302 clinical medicine ,In vivo ,Stomach Neoplasms ,Cell Line, Tumor ,medicine ,Humans ,Clinical significance ,Esophagogastric junction ,Aged ,Pharmacology ,Aged, 80 and over ,Trametes ,business.industry ,medicine.disease ,MAP Kinase Kinase Kinases ,Prognosis ,In vitro ,030104 developmental biology ,Treatment Outcome ,Cell culture ,Tissue Array Analysis ,030220 oncology & carcinogenesis ,Toxicity ,Cancer research ,Esophagogastric Junction ,business - Abstract
The incidence rate of adenocarcinoma of the esophagogastric junction (AEG) is increasing worldwide with poor prognosis and unclear pathogenesis. Trametes robiniophila Murr. (Huaier), a traditional Chinese medicine has been used in the clinical treatment of a variety of solid tumors, including AEG. However, its anticancer components and molecular mechanisms are still unclear. In our previous studies, we have found that Huaier n-butanol extract (HBE) shows the most potent anticancer activity among different extracts. In the present study, we aimed to investigate the clinical relevance of p-MEK expression in AEG patients and the role of the MEK/ERK signaling pathway in the anti-AEG efficacy of HBE in vitro and in vivo. We herein demonstrate that p-MEK expression in AEG tissues was significantly higher than that in paracancerous tissues and correlated with a poor prognosis in AEG patients. We further found that HBE inhibited the colony formation, migration, and invasion in AEG cell lines in a concentration-dependent manner in vitro. HBE also suppressed the growth of AEG xenograft tumors without causing any host toxicity in vivo. Mechanistically, HBE caused the inactivation of the MEK/ERK signaling pathway by dephosphorylating MEK1 at S298, ERK1 at T202, and ERK2 at T185 and modulating the expression of EMT-related proteins. In summary, our results demonstrate that the high expression of p-MEK may be an independent factor of poor prognosis in patients with AEG. The clinically used anticancer drug Huaier may exert its anti-AEG efficacy by inhibiting the MEK/ERK signaling pathway.
- Published
- 2020