Astragalus membranaceus (Huangqi) and Rhizoma curcumae (Ezhu) decoction suppresses colorectal cancer via downregulation of Wnt5/β-Catenin signal

被引:33
作者
Bian, Yong [1 ]
Wang, Gang [1 ]
Zhou, Jing [2 ]
Yin, Gang [3 ,4 ]
Liu, Tiantian [3 ,4 ]
Liang, Li [3 ,4 ]
Yang, Xinyue [3 ,4 ]
Zhang, Wen [5 ]
Ni, Kexin [6 ]
Tang, Decai [3 ,4 ]
Yu, Yun [6 ]
机构
[1] Nanjing Univ Chinese Med, Lab Anim Ctr, Nanjing 210023, Peoples R China
[2] Sichuan Acad Chinese Med Sci, Ctr Expt Anim, Chengdu 610041, Peoples R China
[3] Nanjing Univ Chinese Med, Sch Tradit Chinese Med, Nanjing 210023, Peoples R China
[4] Nanjing Univ Chinese Med, Sch Integrated Chinese & Western Med, Nanjing 210023, Peoples R China
[5] Nanjing Med Univ, Jiangsu Key Lab Oral Dis, Nanjing 211166, Peoples R China
[6] Nanjing Univ Chinese Med, Sch Pharm, Nanjing 210023, Peoples R China
基金
中国国家自然科学基金;
关键词
Astragalus membranaceus; Rhizoma curcumae; Wnt5; beta-Catenin; Colorectal cancer; CELL-GROWTH; PROTEIN; PHAEOCAULIS; EXTRACTS;
D O I
10.1186/s13020-021-00564-6
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Background: The decoction of Astragalus membranaceus (Huangqi) and Rhizoma curcumae (Ezhu) has been reported as a potential antitumor agent for colorectal cancer (CRC) in experimental and clinical studies, but its underlying mechanism is still unclear. Methods: The current research aims to explore the potential of Astragalus membranaceus (Huangqi) and Rhizoma curcumae (Ezhu) decoction (AR decoction) in the treatment of CRC and explore the underlying mechanism. SW620 cells were transient transfection to overexpress or knock down wnt 5 or beta-Catenin. Astragalus membranaceus (Huangqi) and Rhizoma curcumae (Ezhu) -containing serum (AR-CS) was used to interfere with SW620 cells. Additional AR-CS, Wnt5 inhibitor (IWP-4), and beta-Catenin inhibitor (JW55) were used to intervene in SW620 cells. Furthermore, subcutaneously injection of SW620 cells into the right flank of nude mice replicated xenograft mice, which were treated with AR decoction for 21 days. Results: AR-CS significantly reduced the mRNA and protein expression levels of Wnt5, beta-Catenin, ARF6, and N-Cadherin in SW620 cells, while inhibiting the proliferation and migration of SW620 cells. In cells overexpressing Wnt5 or beta-Catenin, these effects of AR-CS were significantly suppressed. On the contrary, the inhibitory effect of AR-CS on the mRNA and protein levels of ARF6 and N-Cadherin and cell proliferation and migration of SW620 was enhanced, when Wnt5 or beta-Catenin were knocked down or suppressed by the inhibitors. Moreover, in the mouse model of xenograft tumors, AR decoction not only reduced the tumor volume and inhibited the mRNA levels and protein levels of Wnt5, P-Catenin, ARF6, and N-Cadherin in the tumor, but also inhibit the protein levels of LRP5, LRP6, TCF-4, and LEF1.The histopathology of mice also showed increased apoptosis in tumor tissues, and AR decoction treatment did not cause pathological damage to the kidney and liver. Conclusions: Our results provide evidence that AR decoction inhibits Wnt5/beta-catenin signaling and inhibits the development of CRC, which is a promising traditional medicine in the clinical treatment of CRC.
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页数:18
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