Natural polysaccharides exhibit anti-tumor activity by targeting gut microbiota

被引:137
作者
Liu, Liqiao [1 ]
Li, Mingzhu [2 ]
Yu, Mulan [3 ]
Shen, Mingyue [4 ]
Wang, Qun [5 ]
Yu, Yue [4 ]
Xie, Jianhua [4 ]
机构
[1] Nanchang Univ, Affiliated Hosp 2, Nanchang 330000, Jiangxi, Peoples R China
[2] Nanchang Univ, Med Coll, Nanchang 330000, Jiangxi, Peoples R China
[3] Luodian Hosp, Dept Obstet & Gynecol, Shanghai 201908, Peoples R China
[4] Nanchang Univ, State Key Lab Food Sci & Technol, Nanchang 330047, Jiangxi, Peoples R China
[5] Nanchang Univ, Affiliated Hosp 1, Dept Cardiovasc Surg, Nanchang 330000, Jiangxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Polysaccharides; Gut microbiota; Anti-tumor; REGULATORY T-CELLS; CHAIN FATTY-ACIDS; ANTIOXIDANT ACTIVITIES; COLORECTAL-CANCER; BIOACTIVE POLYSACCHARIDES; IMMUNOMODULATORY ACTIVITY; INTESTINAL MICROBIOTA; SULFATED MODIFICATION; BREAST-CANCER; LIVER-CANCER;
D O I
10.1016/j.ijbiomac.2018.10.083
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Natural polysaccharides, the abundant dietary components, show potent antitumor bioactivity in treatment and chemoprevention. Compared with traditional tumor therapy, natural polysaccharides are characterized by the low toxicity and immuno-regulation function. Recent researches have indicated that the anti-tumor of polysaccharides was partly attributable to modification in the composition of gut microbiota when polysaccharides were digested. Indeed, microbial dysbiosis or alteration of certain bacterial species has been reported in tumorigenesis. Natural polysaccharides intake can reverse such changes by enriching health-promoting bacteria and metabolite the intestine. In this review, we first summarize current knowledge on the anti-tumor activity of polysaccharides, and demonstrate the relationship between bacteria and metabolite in the intestine tumorigenesis and microbial dysbiosis. Thereafter, and the "polysaccharides-gut microbiota" is put forward for polysaccharides to exhibit their antitumor activity, which may attribute to the improved leaky gut, avoided hypernutrition, and reinforced immune homeostasis, finally creating a systemic environment to lower the risks of tumor. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:743 / 751
页数:9
相关论文
共 109 条
[1]   DSS colitis promotes tumorigenesis and fibrogenesis in a choline-deficient high-fat diet-induced NASH mouse model [J].
Achiwa, Koichi ;
Ishigami, Masatoshi ;
Ishizu, Yoji ;
Kuzuya, Teiji ;
Honda, Takashi ;
Hayashi, Kazuhiko ;
Hirooka, Yoshiki ;
Katano, Yoshiaki ;
Goto, Hidemi .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2016, 470 (01) :15-21
[2]   Biological effects of propionic acid in humans; metabolism, potential applications and underlying mechanisms [J].
Al-Lahham, Sa'ad H. ;
Peppelenbosch, Maikel P. ;
Roelofsen, Han ;
Vonk, Roel J. ;
Venema, Koen .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2010, 1801 (11) :1175-1183
[3]   Dual role of tumour-infiltrating T helper 17 cells in human colorectal cancer [J].
Amicarella, F. ;
Muraro, M. G. ;
Hirt, C. ;
Cremonesi, E. ;
Padovan, E. ;
Mele, V. ;
Governa, V. ;
Han, J. ;
Huber, X. ;
Droeser, R. A. ;
Zuber, M. ;
Adamina, M. ;
Bolli, M. ;
Rosso, R. ;
Lugli, A. ;
Zlobec, I. ;
Terracciano, L. ;
Tornillo, L. ;
Zajac, P. ;
Eppenberger-Castori, S. ;
Trapani, F. ;
Oertli, D. ;
Iezzi, G. .
GUT, 2017, 66 (04) :692-704
[4]  
[Anonymous], PHYSL REP
[5]  
[Anonymous], 2018, Bioact. Carbohydr. Diet. Fibre, DOI DOI 10.1016/J.BCDF.2018.04.002
[6]  
[Anonymous], J PHARM SCI
[7]  
[Anonymous], CANC DISCOV
[8]  
[Anonymous], 2018, SCI REP-UK, DOI DOI 10.1038/s41598-018-22885-7
[9]   The immunomodulatory activities of licorice polysaccharides (Glycyrrhiza uralensis Fisch.) in CT 26 tumor-bearing mice [J].
Ayeka, Peter Amwoga ;
Bian, YuHong ;
Githaiga, Peter Mwitari ;
Zhao, Ying .
BMC COMPLEMENTARY AND ALTERNATIVE MEDICINE, 2017, 17
[10]   Microbiota-activated PPAR-γ signaling inhibits dysbiotic Enterobacteriaceae expansion [J].
Byndloss, Mariana X. ;
Olsan, Erin E. ;
Rivera-Chavez, Fabian ;
Tiffany, Connor R. ;
Cevallos, Stephanie A. ;
Lokken, Kristen L. ;
Torres, Teresa P. ;
Byndloss, Austin J. ;
Faber, Franziska ;
Gao, Yandong ;
Litvak, Yael ;
Lopez, Christopher A. ;
Xu, Gege ;
Napoli, Eleonora ;
Giulivi, Cecilia ;
Tsolis, Renee M. ;
Revzin, Alexander ;
Lebrilla, Carlito B. ;
Baumler, Andreas J. .
SCIENCE, 2017, 357 (6351) :570-+