Shi Yunfu, Yuan Li, Xu Jingli, Xu Handong, Wang Lijing, Huang Ling, Xu Zhiyuan, Cheng Xiangdong
Tongde Hospital Affiliated to Zhejiang Chinese Medical University (Tongde Hospital of Zhejiang Province), Hangzhou 310012, China.
The First Clinical Medical College of Zhejiang Chinese Medical University, Hangzhou, Zhejiang 310053, China.
J Oncol. 2022 Jun 15;2022:6065516. doi: 10.1155/2022/6065516. eCollection 2022.
Gastric cancer (GC) is a common malignant tumor worldwide and poses a serious threat to human health. As a traditional Chinese medicine, Huaier ( Murr.) has been used in the clinical treatment of GC. However, the mechanism underlying the anticancer effect of Huaier remains poorly understood. In this study, we used imaging technology to determine the anticancer effect of the Huaier n-butanol extract (HBE) on orthotopic and hepatic metastasis of GC mouse models. We found that HBE suppressed tumor growth and metastasis without causing apparent host toxicity. Proteomic analysis of GC cells before and after HBE intervention revealed syntenin to be one of the most significantly downregulated proteins after HBE intervention. We further demonstrated that HBE suppressed the growth and metastasis of GC by reducing the expression of syntenin and the phosphorylation of STAT3 at Y705 and reversing the epithelial-mesenchymal transition (EMT). In addition, we confirmed that syntenin was highly expressed in GC tissue and correlated with metastasis and poor prognosis. In conclusion, our results suggest that Huaier, a clinically used anticancer drug, may inhibit the growth and liver metastasis of GC by inhibiting the syntenin/STAT3 signaling pathway and reversing EMT.
胃癌(GC)是全球常见的恶性肿瘤,对人类健康构成严重威胁。槐耳(Murr.)作为一种传统中药,已用于GC的临床治疗。然而,槐耳抗癌作用的潜在机制仍知之甚少。在本研究中,我们使用成像技术确定槐耳正丁醇提取物(HBE)对GC小鼠原位和肝转移模型的抗癌作用。我们发现HBE可抑制肿瘤生长和转移,且不会引起明显的宿主毒性。对HBE干预前后的GC细胞进行蛋白质组学分析,结果显示syntenin是HBE干预后下调最显著的蛋白质之一。我们进一步证明,HBE通过降低syntenin的表达以及Y705位点STAT3的磷酸化水平,并逆转上皮-间质转化(EMT),从而抑制GC的生长和转移。此外,我们证实syntenin在GC组织中高表达,且与转移和不良预后相关。总之,我们的结果表明,临床上使用的抗癌药物槐耳可能通过抑制syntenin/STAT3信号通路和逆转EMT来抑制GC的生长和肝转移。