Mechanism of traditional drug treatment of cancer-related ascites: through the regulation of IL-6/JAK-STAT3 pathway

被引:1
|
作者
Sun, Yehan [1 ]
Zhang, Pengcheng [2 ]
Ma, Jia [1 ]
Chen, Youmou [1 ]
Huo, Xingxing [3 ]
Song, Hang [4 ]
Zhu, Yongfu [5 ]
机构
[1] Anhui Univ Tradit Chinese Med, Grad Sch, Hefei, Peoples R China
[2] Zhejiang Chinese Med Univ, Affiliated Hosp 1, Zhejiang Prov Hosp Chinese Med, Hangzhou, Peoples R China
[3] Anhui Univ Chinese Med, Affiliated Hosp 1, Expt Ctr Clin Res, Sci Res Dept, Hefei, Peoples R China
[4] Anhui Univ Chinese Med, Sch Integrated Chinese & Western Med, Dept Biochem & Mol Biol, Hefei, Peoples R China
[5] Anhui Univ Chinese Med, Affiliated Hosp 1, Dept Oncol 1, Hefei, Peoples R China
基金
安徽省自然科学基金;
关键词
malignant ascites; Jijiao Lihuang Pill; Network Pharmacology; molecular docking; potential mechanisms; MODEL;
D O I
10.1093/jpp/rgae111
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Context: Our clinical observation found that JiJiaoLiHuang Pill (JJLH), a classic traditional Chinese medicine (TCM) formulation, can significantly reduce the abdominal circumference of patients with malignant ascites, increase urine output, and improve the quality of life of patients, with preliminary efficacy. But, the exact mechanism is not yet clear. Objective: Based on the above observations, the potential mechanism of action of the treatment was preliminarily explored. Methods: We identified active ingredients by constructing a "Chinese medicine ingredient-key target-target" network, and verified them by molecular docking using AutoDock tools and PyMOL. Finally, we conducted preliminary verification of the validated pathways and targets using a mouse model of liver cancer ascites. Results: Network pharmacology analysis obtained the top five active ingredients were quercetin, EUPATIN, kaempferol, Obtucarbamate B, and isorhamnetin and the top five key genes were SRC, HSP90AA1, MAPK1, STAT3, and PIK3CA. Molecular docking showed that all 5 active compounds were closely bound to key target genes (binding energy <-6). The animal experiment results showed that JJLH can significantly reduce abdominal circumference, increase urine output, and exhibit dose-dependent inhibition of the AQP-3/JAK-STAT-3 signaling pathway and the expression of related inflammatory factors. Conclusions: The JJLH potentially inhibits the recurrence of liver cancer malignant ascites through the AQP-3/JAK-STAT-3 pathway and affects the prognosis of MA patients.
引用
收藏
页码:264 / 274
页数:11
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