Expression analysis of Cdc42 in lung cancer and modulation of its expression by curcumin in lung cancer cell lines

被引:58
作者
Chen, Qing-Yong [1 ,2 ]
Jiao, De-Min [2 ]
Yao, Qing-Hua [3 ]
Yan, Jie [2 ]
Song, Jia [2 ]
Chen, Fang-Yuan [2 ]
Lu, Guo-Hua [1 ]
Zhou, Jan-Ying [1 ]
机构
[1] Zhejiang Univ, Coll Med, Affiliated Hosp 1, Dept Resp Dis, Hangzhou 310003, Zhejiang, Peoples R China
[2] 117th Hosp PLA, Dept Resp Dis, Hangzhou 310003, Zhejiang, Peoples R China
[3] Zhejiang Chinese Med Univ, Affiliated Hosp 1, Dept Oncol, Hangzhou 310053, Zhejiang, Peoples R China
关键词
Cdc42; RNA interference; actin cytoskeleton; migration and invasion; lung cancer; lung cancer cell lines; curcumin; EPIDERMAL-GROWTH-FACTOR; RHO-GTPASES; UP-REGULATION; MIGRATION; ADHESION; ADENOCARCINOMA; PROLIFERATION; DEGRADATION; INVOLVEMENT; INHIBITION;
D O I
10.3892/ijo.2012.1336
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cdc42, a Rho GTPase family member, is involved in cell transformation, proliferation, survival, invasion and metastasis of human cancer cells. Overexpression of Cdc42 has been reported in several types of human cancer. However, the underlying mechanisms are not well understood. The present study showed that Cdc42 was overexpressed in 80 of 110 primary lung cancer patients, and overexpression of Cdc42 was significantly associated with high TNM stage and lymph node metastasis. Moreover, RNAi-mediated suppression of Cdc42 expression reduced actin filopodia formation, migration and invasion potential of a highly metastatic lung cancer cell line, 801D. In parallel, 801D cells were treated with curcumin and the effect on the expression of the Cdc42 gene at the transcriptional and translational levels was analyzed by RT-PCR and Western blotting. Curcumin inhibited cell migration, invasion and downregulated Cdc42 gene and Cdc42-related target gene expression in 801D cells. It also induced rearrangements of the actin cytoskeleton. These effects mimicked those of Cdc42 knockdown. Furthermore, xenograft experiments confirmed the suppression of tumor growth and invasion in vivo, which was due to the effect of curcumin and the inhibition of Cdc42 by curcumin. Our results showing the downregulation of Cdc42 expression by curcumin in lung cancer cells taken together with the clinical data suggest a potential therapeutic role for curcumin in inducing Cdc42-mediated inhibition of invasion of lung cancer cells.
引用
收藏
页码:1561 / 1568
页数:8
相关论文
共 31 条
  • [1] Curcumin (diferuloylmethane) down-regulates expression of cell proliferation and antiapoptotic and metastatic gene products through suppression of IκBα kinase and Akt activation
    Aggarwal, S
    Ichikawa, H
    Takada, Y
    Sandur, SK
    Shishodia, S
    Aggarwal, BB
    [J]. MOLECULAR PHARMACOLOGY, 2006, 69 (01) : 195 - 206
  • [2] Cell attachment to the extracellular matrix induces proteasomal degradation of p21CIP1 via Cdc42/Rac1 signaling
    Bao, WJ
    Thullberg, M
    Zhang, HQ
    Onischenko, A
    Strömblad, S
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (13) : 4587 - 4597
  • [3] The transcriptional network for mesenchymal transformation of brain tumours
    Carro, Maria Stella
    Lim, Wei Keat
    Alvarez, Mariano Javier
    Bollo, Robert J.
    Zhao, Xudong
    Snyder, Evan Y.
    Sulman, Erik P.
    Anne, Sandrine L.
    Doetsch, Fiona
    Colman, Howard
    Lasorella, Anna
    Aldape, Ken
    Califano, Andrea
    Iavarone, Antonio
    [J]. NATURE, 2010, 463 (7279) : 318 - U68
  • [4] Curcumin inhibits lung cancer cell invasion and metastasis through the tumor suppressor HLJ1
    Chen, Huei-Wen
    Lee, Jen-Yi
    Huang, Ji-Ying
    Wang, Chi-Chung
    Chen, Wan-Jiun
    Su, Sheng-Fang
    Huang, Chia-Wen
    Ho, Chao-Chi
    Chen, Jeremy J. W.
    Tsai, Meng-Feng
    Yu, Sung-Liang
    Yang, Pan-Chyr
    [J]. CANCER RESEARCH, 2008, 68 (18) : 7428 - 7438
  • [5] Curcumin induces apoptosis in human lung adenocarcinoma A549 cells through a reactive oxygen species-dependent mitochondrial signaling pathway
    Chen, Qingyong
    Wang, Yanyi
    Xu, Kedi
    Lu, Guohua
    Ying, Zheng
    Wu, Lijun
    Zhan, Jianwei
    Fang, Rui
    Wu, Yuquan
    Zhou, Jianying
    [J]. ONCOLOGY REPORTS, 2010, 23 (02) : 397 - 403
  • [6] Del Pulgar TG, 2008, INT J ONCOL, V33, P185
  • [7] Fritz G, 1999, INT J CANCER, V81, P682, DOI 10.1002/(SICI)1097-0215(19990531)81:5<682::AID-IJC2>3.0.CO
  • [8] 2-B
  • [9] Growth and motility inhibition of breast cancer cells by epidermal growth factor receptor degradation is correlated with inactivation of Cdc42
    Hirsch, DS
    Shen, Y
    Wu, WJ
    [J]. CANCER RESEARCH, 2006, 66 (07) : 3523 - 3530
  • [10] Up-regulation of small GTPases, RhoA and RhoC, is associated with tumor progression in ovarian carcinoma
    Horiuchi, A
    Imai, T
    Wang, CJ
    Ohira, S
    Feng, YZ
    Nikaido, T
    Konishi, I
    [J]. LABORATORY INVESTIGATION, 2003, 83 (06) : 861 - 870