Matrine derivative YF-18 inhibits lung cancer cell proliferation and migration through down-regulating Skp2

被引:23
作者
Wu, Lichuan [1 ]
Wang, Guizhen [2 ]
Wei, Jinrui [3 ]
Huang, Na [4 ]
Zhang, Sen [1 ]
Yang, Fangfang [1 ]
Li, Ming [5 ]
Zhou, Guangbiao [2 ]
Wang, Lisheng [1 ]
机构
[1] Guangxi Univ, Sch Chem & Chem Engn, Nanning, Guangxi, Peoples R China
[2] Chinese Acad Sci, Inst Zool, State Key Lab Membrane Biol, Beijing, Peoples R China
[3] Guangxi Univ Chinese Med, Guangxi Sci Res Ctr Tradit Chinese Med, Nanning, Guangxi, Peoples R China
[4] Guangxi Med Univ, Affiliated Tumour Hosp, Nanning, Guangxi, Peoples R China
[5] Chinese Acad Sci & Yunnan Prov, Kunming Inst Zool, Key Lab Anim Models & Human Dis Mech, Kunming, Yunnan, Peoples R China
基金
国家杰出青年科学基金; 中国博士后科学基金; 中国国家自然科学基金;
关键词
lung cancer; matrine derivative; Skp2; proliferation; migration; IN-VITRO; TARGET; P27; DEGRADATION; P27(KIP1); APOPTOSIS; PATHWAY; PROTEIN; CYCLE; UBIQUITINATION;
D O I
10.18632/oncotarget.14329
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Lung cancer is the leading cause of cancer related death which needs novel drugs to improve patient outcomes. In this study, we examined the ability of YF-18, a novel matrine derivative to inhibit the growth and migration of lung cancer cells. By cell cycle analysis, wound healing and transwell assays, we found that YF-18 induced G2/M cell cycle arrest and inhibited migration of lung cancer cells in a dose-dependent manner. Further results indicated that YF-18 inhibited cell proliferation and migration through down-regulating Skp2 and up-regulating its substrates, p27 and E-cadherin. Moreover, YF-18 inhibited A549-luciferase cell xenograft tumor growth in a dosedependent manner. The findings indicate that YF-18 bears therapeutic potentials for
引用
收藏
页码:11729 / 11738
页数:10
相关论文
共 50 条
[1]
Skp2 A dream target in the coming age of cancer therapy [J].
Chan, Chia-Hsin ;
Morrow, John Kenneth ;
Zhang, Shuxing ;
Lin, Hui-Kuan .
CELL CYCLE, 2014, 13 (05) :679-680
[2]
Chen Jian, 2006, Zhong Xi Yi Jie He Xue Bao, V4, P78
[3]
Targeting the p27 E3 ligase SCFSkp2 results in p27-and Skp2-mediated cell-cycle arrest and activation of autophagy [J].
Chen, Qing ;
Xie, Weilin ;
Kuhn, Deborah J. ;
Voorhees, Peter M. ;
Lopez-Girona, Antonia ;
Mendy, Derek ;
Corral, Laura G. ;
Krenitsky, Veronique Plantevin ;
Xu, Weiming ;
Parseval, Laure Moutouh-de ;
Webb, David R. ;
Mercurio, Frank ;
Nakayama, Keiichi I. ;
Nakayama, Keiko ;
Orlowski, Robert Z. .
BLOOD, 2008, 111 (09) :4690-4699
[4]
Exceeding the limit of plasmonic light trapping in textured screen-printed solar cells using Al nanoparticles and wrinkle-like graphene sheets [J].
Chen, Xi ;
Jia, Baohua ;
Zhang, Yinan ;
Gu, Min .
LIGHT-SCIENCE & APPLICATIONS, 2013, 2 :e92-e92
[5]
Guan Cheng-Nong, 2006, Zhongguo Zhong Yao Za Zhi, V31, P510
[6]
E3 ubiquitin ligase Skp2 as an attractive target in cancer therapy [J].
Hao, Zhonglin ;
Huang, Shuang .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2015, 20 :474-490
[7]
Molecular origins of cancer: Lung cancer [J].
Herbst, Roy S. ;
Heymach, John V. ;
Lippman, Scott M. .
NEW ENGLAND JOURNAL OF MEDICINE, 2008, 359 (13) :1367-1380
[8]
[胡鹏翼 Hu Pengyi], 2012, [中国新药杂志, Chinese Journal New Drugs], V21, P2662
[9]
Huang Sixia, 2011, Zhongguo Zhong Yao Za Zhi, V36, P3198
[10]
Skp2 overexpression increases the expression of MMP-2 and MMP-9 and invasion of lung cancer cells [J].
Hung, Wen-Chun ;
Tseng, Wei-Lung ;
Shiea, Jentaie ;
Chang, Hui-Chiu .
CANCER LETTERS, 2010, 288 (02) :156-161