18α-glycyrrhetinic acid suppresses gastric cancer by activation of miR-149-3p-Wnt-1 signaling

被引:49
作者
Cao, Donghui [1 ]
Jia, Zhifang [1 ]
You, Lili [1 ]
Wu, Yanhua [1 ]
Hou, Zhen [2 ]
Suo, Yueer [2 ]
Zhang, Houjun [2 ]
Wen, Simin [1 ]
Tsukamoto, Tetsuya [3 ]
Oshima, Masanobu [4 ]
Jiang, Jing [1 ]
Cao, Xueyuan [2 ]
机构
[1] Jilin Univ, Hosp 1, Div Clin Res, Changchun 130021, Jilin, Peoples R China
[2] Jilin Univ, Hosp 1, Dept Gastr & Colorectal Surg, Changchun 130021, Jilin, Peoples R China
[3] Fujita Hlth Univ, Sch Med, Dept Diagnost Pathol 1, Toyoake, Aichi 4701192, Japan
[4] Kanazawa Univ, Canc Res Inst, Kanazawa, Ishikawa 9201192, Japan
基金
中国国家自然科学基金;
关键词
18 beta-glycyrrhetinic acid; gastric cancer; COX-2; miR-149-3p; Wnt-1; GLYCYRRHETINIC ACID; TUMOR-SUPPRESSOR; 18-BETA-GLYCYRRHETINIC ACID; INHIBITS PROLIFERATION; CHRONIC INFLAMMATION; CELL-PROLIFERATION; CARCINOMA; METASTASIS; CARCINOGENESIS; MICRORNA-149;
D O I
10.18632/oncotarget.12443
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
18 beta-glycyrrhetinic acid (GRA) exerts anti-tumor effects on various types of cancer. In the present study, we found that GRA attenuated the severity of gastritis and suppressed gastric tumorigenesis in transgenic mice. We also discovered that miR-149-3p was downregulated in gastric cancer tissues and cell lines as compared to normal gastric tissues and epithelial cells, but was upregulated by GRA. miR-1493-p expression also correlated negatively with lymphnode metastasis. Our functional assays showed that miR-149-3p overexpression inhibited cell proliferation and cell cycle progression while inducing apoptosis, while inhibition of miR-149-3p had the opposite effects. In addition, we identified Wnt-1 as a direct target of miR-149-3p. These data suggest that GRA inhibits the initiation and progression of gastric tumors by ameliorating the inflammatory microenvironment through downregulation of COX-2 expression and by inhibiting Wnt-1 expression through the upregulation of tumor suppressor miR-149-3p. GRA may thus have the potential to serve as a useful therapeutic agent for the prevention and treatment of gastric cancer.
引用
收藏
页码:71960 / 71973
页数:14
相关论文
共 47 条
[1]  
[Anonymous], COCHRANE DATABASE SY
[2]  
[Anonymous], EVIDENCE BASED COMPL
[3]   miR149 Functions as a Tumor Suppressor by Controlling Breast Epithelial Cell Migration and Invasion [J].
Bischoff, Annabell ;
Huck, Bettina ;
Keller, Bettina ;
Strotbek, Michaela ;
Schmid, Simone ;
Boerries, Melanie ;
Busch, Hauke ;
Mueller, Dafne ;
Olayioye, Monilola A. .
CANCER RESEARCH, 2014, 74 (18) :5256-5265
[4]   The Protective Effects of 18β-Glycyrrhetinic Acid on Helicobacter pylori-Infected Gastric Mucosa in Mongolian Gerbils [J].
Cao, Donghui ;
Jiang, Jing ;
You, Lili ;
Jia, Zhifang ;
Tsukamoto, Tetsuya ;
Cai, Hongke ;
Wang, Shidong ;
Hou, Zhen ;
Suo, Yue-er ;
Cao, Xueyuan .
BIOMED RESEARCH INTERNATIONAL, 2016, 2016
[5]   Canolol Inhibits Gastric Tumors Initiation and Progression through COX-2/PGE2 Pathway in K19-C2mE Transgenic Mice [J].
Cao, Donghui ;
Jiang, Jing ;
Tsukamoto, Tetsuya ;
Liu, Ruming ;
Ma, Lin ;
Jia, Zhifang ;
Kong, Fei ;
Oshima, Masanobu ;
Cao, Xueyuan .
PLOS ONE, 2015, 10 (03)
[6]   Severity of gastritis determines glandular stomach carcinogenesis in Helicobacter pylori-infected Mongolian gerbils [J].
Cao, Xueyuan ;
Tsukamoto, Tetsuya ;
Nozaki, Koji ;
Tanaka, Harunari ;
Cao, Liyu ;
Toyoda, Takeshi ;
Takasu, Shinji ;
Ban, Hisayo ;
Kumagai, Toshiko ;
Tatematsu, Masae .
CANCER SCIENCE, 2007, 98 (04) :478-483
[7]   MicroRNA-149 targets GIT1 to suppress integrin signaling and breast cancer metastasis [J].
Chan, S-H ;
Huang, W-C ;
Chang, J-W ;
Chang, K-J ;
Kuo, W-H ;
Wang, M-Y ;
Lin, K-Y ;
Uen, Y-H ;
Hou, M-F ;
Lin, C-M ;
Jang, T-H ;
Tu, C-W ;
Lee, Y-R ;
Lee, Y-H ;
Tien, M-T ;
Wang, L-H .
ONCOGENE, 2014, 33 (36) :4496-4507
[8]   Dual inhibitory effect of Glycyrrhiza glabra (GutGard™) on COX and LOX products [J].
Chandrasekaran, C. V. ;
Deepak, H. B. ;
Thiyagarajan, P. ;
Kathiresan, S. ;
Sangli, Gopal Krishna ;
Deepak, M. ;
Agarwal, Amit .
PHYTOMEDICINE, 2011, 18 (04) :278-284
[9]  
Chen W, 2016, CA CANC J CLIN
[10]  
Chiurillo MA, 2015, WORLD J EXP MED, V5, P84, DOI [DOI 10.5493/WJEM.V5.I2.84, 10.5493/wjem.v5.i2.84]