2,3,5,4′-tetrahydroxystilbene-2-O-β-D-glucoside suppresses human colorectal cancer cell metastasis through inhibiting NF-κB activation

被引:16
|
作者
Lin, Chien-Liang [1 ]
Hsieh, Shu-Ling [3 ]
Leung, Wan [2 ]
Jeng, Jiiang-Huei [4 ]
Huang, Guan-Cheng [5 ]
Lee, Chining-Ting [3 ]
Wu, Chih-Chung [6 ]
机构
[1] Yuans Gen Hosp, Dept Pharm, Kaohsiung 802, Taiwan
[2] Yuans Gen Hosp, Dept Radiol & Nucl Med, Kaohsiung 802, Taiwan
[3] Natl Kaohsiung Marine Univ, Dept Seafood Sci, Kaohsiung 811, Taiwan
[4] Natl Taiwan Univ Hosp, Dept Dent, Taipei 100, Taiwan
[5] Fooyin Univ, Sch Nursing, Dept Hlth Business Adm, Kaohsiung 831, Taiwan
[6] Chang Jung Christian Univ, Dept Nutr & Hlth Sci, 1 Changda Rd, Tainan 711, Taiwan
关键词
2,3,5,4 '-tetrahydroxystilbene-2-O-beta-D-glucoside; migration; invasion; adhesion; metastasis; NF-kappa B; human colorectal cancer cells; PROSTATE-CANCER; TETRAHYDROXYSTILBENE GLUCOSIDE; MATRIX-METALLOPROTEINASE; MMP-2; EXPRESSION; E-SELECTIN; IN-VITRO; INVASION; ADHESION; PROLIFERATION; PROTEINS;
D O I
10.3892/ijo.2016.3574
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
2,3, 5,4'-tetrahydroxystilbene-2-O-beta-D-glucoside (THSG), a major component of Polygonum multiflorum Thunb (He-Shou-Wu), has been reported to exhibit antioxidant and anti-inflammatory effects. However, its anti-metastatic effect against colorectal cancer is still unclear. In this study, cell migration, invasion and adhesion abilities as well as metastasis-associated protein and NF-kappa B pathway signaling factor expression were analyzed after treating HT-29 cells with THSG. According to the results, the migration and invasiveness of HT-29 cells were reduced after treatment with 5 or 10 mM THSG (p<0.05). Additionally, the levels of matrix metalloproteinase-2 (MMP-2) and phosphorylated VE-cadherin in HT-29 cells were reduced and the transepithelial electrical resistance (TEER) of EA.hy926 endothelial cell monolayers was increased after incubation in THSG for 24 h (p<0.05). Cell adhesion ability and the E-selectin and intercellular adhesion molecule-1 (ICAM-1) protein levels were reduced when EA.hy926 endothelial cells were treated with THSG (p<0.05). In addition, the cytoplasmic phosphorylation of I kappa B, the nuclear p65 level and the DNA-binding activity of NF-kappa B were reduced after treating HT-29 or EA.hy926 cells with 5 or 10 mM THSG (p<0.05). These results suggest that THSG inhibits HT-29 cell metastasis by suppressing cell migration, invasion and adhesion. Furthermore, THSG inhibits metastasis-associated protein expression by suppressing NF-kappa B pathway activation.
引用
收藏
页码:629 / 638
页数:10
相关论文
共 50 条
  • [21] 2,3,5,4′-Tetrahydroxystilbene-2-O-β-glucoside Isolated from Polygoni Multiflori Ameliorates the Development of Periodontitis
    Chin, Yu-Tang
    Hsieh, Meng-Ti
    Lin, Chi-Yu
    Kuo, Po-Jan
    Yang, Yu-Chen S. H.
    Shih, Ya-Jung
    Lai, Hsuan-Yu
    Cheng, Guei-Yun
    Tang, Heng-Yuan
    Lee, Chen-Chen
    Lee, Sheng-Yang
    Wang, Ching-Chiung
    Lin, Hung-Yun
    Fu, Earl
    Whang-Peng, Jacqueline
    Liu, Leroy F.
    MEDIATORS OF INFLAMMATION, 2016, 2016
  • [22] 2,3,5,4′-Tetrahydroxystilbene-2-O-β-d-glucoside eliminates ischemia/reperfusion injury-induced H9c2 cardiomyocytes apoptosis involving in Bcl-2, Bax, caspase-3, and Akt activation
    Sun, Tao
    Liu, Han
    Cheng, Yutong
    Yan, Lixiao
    Krittanawong, Chayakrit
    Li, Shihong
    Qian, Wang
    Su, Wang
    Chen, Xuanzu
    Hou, Xuejian
    Zhang, Hongju
    JOURNAL OF CELLULAR BIOCHEMISTRY, 2019, 120 (07) : 10972 - 10977
  • [23] TSG (2,3,5,4′-Tetrahydroxystilbene-2-O-β-D-glucoside) from the Chinese Herb Polygonum multiflorum Increases Life Span and Stress Resistance of Caenorhabditis elegans
    Buechter, Christian
    Zhao, Liang
    Havermann, Susannah
    Honnen, Sebastian
    Fritz, Gerhard
    Proksch, Peter
    Waetjen, Wim
    OXIDATIVE MEDICINE AND CELLULAR LONGEVITY, 2015, 2015
  • [24] Protective effect of 2,3,5,4'-tetrahydroxystilbene-2-O-β-D-glucoside on aldosterone-induced cardiomyocytes injury via interfering p53 signaling pathway
    Tang, Yu
    Hao, Minghui
    INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL MEDICINE, 2017, 10 (06): : 9029 - +
  • [25] The natural compound 2,3,5,4′-tetrahydroxystilbene-2-O-β-D glucoside protects against adriamycin-induced nephropathy through activating the Nrf2-Keap1 antioxidant pathway
    Lin, En-Yuan
    Bayarsengee, Uyanga
    Wang, Ching-Chiung
    Chiang, Yung-Hsiao
    Cheng, Chao-Wen
    ENVIRONMENTAL TOXICOLOGY, 2018, 33 (01) : 72 - 82
  • [26] 2,3,5,4′-Tetrahydroxystilbene-2-O-β-glucoside Attenuates Reactive Oxygen Species-Dependent Inflammation and Apoptosis in Porphyromonas gingivalis-Infected Brain Endothelial Cells
    Charoensaensuk, Vichuda
    Chen, Yen-Chou
    Lin, Yun-Ho
    Ou, Keng-Liang
    Yang, Liang-Yo
    Lu, Dah-Yuu
    ANTIOXIDANTS, 2022, 11 (04)
  • [27] 2,3,5,4′-tetrahydroxystilbence-2-O-β-D-glucoside attenuates hepatic steatosis via IKKβ/NF-κB and Keapl-Nrf2 pathways in larval zebrafish
    Wang, Cheng
    Hu, Nai-Hua
    Yu, Lin-Yuan
    Gong, Li-Hong
    Dai, Xu-Yang
    Peng, Cheng
    Li, Yun-Xia
    BIOMEDICINE & PHARMACOTHERAPY, 2020, 127
  • [28] Kinetics and mechanism of 2,3,5,4′-tetrahydroxystilbene-2-O-β-D-glycoside (THSG) degradation in aqueous solutions
    Ren, Xiao-liang
    Wang, Gui-fang
    Wang, Meng
    Ou-Yang, Hui-zi
    Qi, Ai-di
    JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2011, 55 (01) : 211 - 215
  • [29] 2,3,5,4-tetrahydroxy diphenylethylene-2-O-glucoside inhibits the adhesion and invasion of A549 human lung cancer cells
    Xu, Ming
    Wang, Cong
    Zhu, Minglin
    Wang, Xianguo
    Zhang, Li
    Zhao, Jinping
    MOLECULAR MEDICINE REPORTS, 2017, 16 (06) : 8900 - 8906
  • [30] 2,3,5,4′-tetrahydroxystilbene-2-O-β-D-glucoside-stimulated dental pulp stem cells-derived conditioned medium enhances cell activity and anti-inflammation
    Chin, Yu-tang
    Liu, Che-ming
    Chen, Ting-yi
    Chung, Yao-yu
    Lin, Chi-yu
    Hsiung, Chao-nan
    Jan, Yun-shen
    Chiu, Hsien-chung
    Fu, Earl
    Lee, Sheng-yang
    JOURNAL OF DENTAL SCIENCES, 2021, 16 (02) : 586 - 598