Zhang Xinrui, Liu Xin, Zhang Yue, Yang Anhui, Zhang Yongfeng, Tong Zhijun, Wang Yingwu, Qiu Ye
Department of Pharmacy, Changchun University of Chinese Medicine, Changchun, China.
School of Life Sciences, Jilin University, Changchun, China.
Front Oncol. 2021 Jul 8;11:696282. doi: 10.3389/fonc.2021.696282. eCollection 2021.
The Wan-Nian-Qing prescription (WNQP), an herbal composite containing , has been used in China for several years for cancer treatment. However, the mechanism of its pharmacological action against liver cancer is not clear. This study aimed to investigate the role of WNQP in inhibiting tumor growth in hepatocellular carcinoma model mice and determine its mechanism of action. We established HepG2- and SMMC-7721-xenografted tumor models in nude mice and BALB/c mice. The mice were administered WNQP for 2 weeks. The bodyweight of each mouse was monitored every day, and the tumor size was measured using vernier caliper before each round of WNQP administration. After the last dose, mice were sacrificed. The tumors were removed, lysed, and subjected to proteome profiling, enzyme-linked immunosorbent assay, and western blotting. The liver, spleen, and kidney were collected for histopathological examination. The effects of WNQP against liver cancer were first systematically confirmed in HepG2- and SMMC-7721-xenografted nude mice and BALB/c mice models. WNQP inhibited tumor growth, but failed to affect bodyweight and organ structures (liver and spleen), confirming that it was safe to use in mice. In BALB/c mice, WNQP regulated immune function, inferred from the modulation of immune-related cytokines such as interleukins, interferon, tumor necrosis factors, and chemokines. Further results confirmed that this regulation occurred the regulatory effects of WNQP on Nrf2 signaling. WNQP can inhibit the growth of HepG2- and SMMC-7721-xenografted tumors in nude mice and BALB/c mice. This effect manifests at least partially through immunomodulation mediated apoptosis.
万年青处方(WNQP)是一种含有[具体成分未给出]的草药组合物,在中国已用于癌症治疗数年。然而,其抗肝癌的药理作用机制尚不清楚。本研究旨在探讨WNQP在抑制肝癌模型小鼠肿瘤生长中的作用,并确定其作用机制。我们在裸鼠和BALB/c小鼠中建立了HepG2和SMMC-7721异种移植肿瘤模型。给小鼠施用WNQP 2周。每天监测每只小鼠的体重,在每轮施用WNQP之前使用游标卡尺测量肿瘤大小。最后一剂后,处死小鼠。取出肿瘤,裂解,并进行蛋白质组分析、酶联免疫吸附测定和蛋白质印迹分析。收集肝脏、脾脏和肾脏进行组织病理学检查。WNQP对肝癌的作用首先在HepG2和SMMC-7721异种移植裸鼠和BALB/c小鼠模型中得到系统证实。WNQP抑制肿瘤生长,但未影响体重和器官结构(肝脏和脾脏),证实其在小鼠中使用是安全的。在BALB/c小鼠中,WNQP调节免疫功能,这可从白细胞介素、干扰素、肿瘤坏死因子和趋化因子等免疫相关细胞因子的调节中推断出来。进一步的结果证实,这种调节是通过WNQP对Nrf2信号通路的调节作用而发生的。WNQP可抑制裸鼠和BALB/c小鼠中HepG2和SMMC-7721异种移植肿瘤的生长。这种作用至少部分通过免疫调节介导的细胞凋亡来体现。