Panax notoginseng saponins prevent colitis-associated colorectal cancer development: the role of gut microbiota

被引:43
作者
Chen Ling [1 ,2 ,3 ]
Chen Man-Yun [2 ,3 ,4 ]
Shao Li [5 ]
Zhang Wei [2 ,3 ,4 ]
Rao Tai [2 ,3 ,4 ]
Zhou Hong-Hao [2 ,3 ,4 ]
Huang Wei-Hua [2 ,3 ,4 ]
机构
[1] Cent South Univ, Xiangya Hosp, Dept Gen Surg, Changsha 410008, Peoples R China
[2] Cent South Univ, Xiangya Hosp, Dept Clin Pharmacol, Changsha 410008, Peoples R China
[3] Cent South Univ, Inst Clin Pharmacol, Hunan Key Lab Pharmacogenet, Changsha 410078, Peoples R China
[4] Cent South Univ, Xiangya Hosp, Natl Clin Res Ctr Geriatr Disorders, Changsha 410008, Peoples R China
[5] Hunan Univ Chinese Med, Sch Pharm, Dept Pharmacognosy, Changsha 410128, Peoples R China
关键词
Panax notoginseng saponins; Gut microbiota; Colorectal cancer; Ginsenosides; 16S rRNA gene sequencing; MEDIATED BIOTRANSFORMATION; AKKERMANSIA-MUCINIPHILA; INTESTINAL MICROBIOTA; INFLAMMATION; GINSENG;
D O I
10.1016/S1875-5364(20)30060-1
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Gut microbiota dysbiosis is a risk factor for colorectal cancer (CRC) in inflammatory bowel disease (IBD). In this study, the effects of Panax notoginseng saponins (PNS) on colitis-associated CRC progression were evaluated on an azoxymethane (AOM)/dextran sulfate sodium (DSS) mouse model. In vivo, PNS significantly relieved AOM/DSS-induced colon tumorigenesis and development by reducing the disease activity index (DAI) scores and colon tumor load. The 16S rRNA data of fecal samples showed that the microbiome community was obviously destructed, while PNS could recover the richness and diversity of gut microbiota. Especially, PNS could increase the abundance of Akkermansia spp. which was significantly decreased in model group and negatively correlated with the progression of CRC. Moreover, ginsenoside compound K (GC-K) was evaluated on the effects of human CRC cells, which was the main bio-transformed metabolite of PNS by gut microbiota. Our data showed that PNS played important role in the prevention of the progression of CRC, due to their regulation on the microbiome balance and microbial bio-converted product with anti-CRC activity.
引用
收藏
页码:500 / 507
页数:8
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