Effects of Lovastatin on MDA-MB-231 Breast Cancer Cells: An Antibody Microarray Analysis

被引:30
作者
Yang, Tao [1 ]
Yao, Hui [2 ]
He, Guangchun [2 ]
Song, Liujiang [2 ]
Liu, Ning [2 ]
Wang, Yan [1 ]
Yang, Yingke [3 ]
Keller, Evan T. [4 ]
Deng, Xiyun [2 ]
机构
[1] Cent South Univ Forestry & Technol, Natl Engn Lab Rice & Byprod Deep Proc, Changsha 410004, Hunan, Peoples R China
[2] Hunan Normal Univ, Coll Med, Changsha 410013, Hunan, Peoples R China
[3] Hunan Univ, Coll Biol, Changsha 410082, Hunan, Peoples R China
[4] Univ Michigan, Dept Urol, Ann Arbor, MI 48109 USA
基金
中国国家自然科学基金;
关键词
Natural products; Lovastatin; Breast cancer; Antibody microarray; Hypoxia; INDUCED APOPTOSIS; DEATH RECEPTOR-3; STATINS; EXPRESSION; TUMOR; DEGRADATION; DOXORUBICIN; METABOLISM; INHIBITOR; TARGET;
D O I
10.7150/jca.13414
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Despite the tremendous improvement in cancer therapeutics, treatment of late-stage breast cancer remains a challenge for both basic scientists and clinicians. Lovastatin, a natural product derived from Aspergillus terreus or Monascus ruber, has been widely used as cholesterol-lowing drug in the clinic. It also has anti-cancer properties through poorly defined molecular mechanisms. In the present study, we employed a novel antibody microarray technology to investigate the molecular mechanisms through which lovastatin inhibits breast cancer. We found that lovastatin up-regulated 17 proteins and down-regulated 20 proteins in MDA-MB-231 breast cancer cells. These included proteins that modulate apoptosis, cell proliferation, differentiation, signal transduction, epithelial-to-mesenchymal transition and tumor metastasis. Modulation of these pathways may mediate, in part, the inhibitory activity of lovastatin on breast cancer.
引用
收藏
页码:192 / 199
页数:8
相关论文
共 35 条
[1]  
Agarwal B, 1999, CLIN CANCER RES, V5, P2223
[2]   Tissue transglutaminase as a central mediator in inflammation-induced progression of breast cancer [J].
Agnihotri, Navneet ;
Kumar, Santosh ;
Mehta, Kapil .
BREAST CANCER RESEARCH, 2013, 15 (01)
[3]   Cancer wars: natural products strike back [J].
Basmadjian, Christine ;
Zhao, Qian ;
Bentouhami, Embarek ;
Djehal, Amel ;
Nebigil, Canan G. ;
Johnson, Roger A. ;
Serova, Maria ;
de Gramont, Armand ;
Faivre, Sandrine ;
Raymond, Eric ;
Desaubry, Laurent G. .
FRONTIERS IN CHEMISTRY, 2014, 2
[4]  
Camirand A, 2013, AM J CANCER RES, V3, P500
[5]   Breast cancer growth prevention by statins [J].
Campbell, Michael J. ;
Esserman, Laura J. ;
Zhou, Yamei ;
Shoemaker, Mark ;
Lobo, Margaret ;
Borman, Elizabeth ;
Baehner, Frederick ;
Kumar, Anjali S. ;
Adduci, Kelly ;
Marx, Corina ;
Petricoin, Emanuel F. ;
Liotta, Lance A. ;
Winters, Mary ;
Benz, Stephen ;
Benz, Christopher C. .
CANCER RESEARCH, 2006, 66 (17) :8707-8714
[6]  
Chan KKW, 2003, CLIN CANCER RES, V9, P10
[7]   Cancer Cell Growth Inhibitory Effect of Bee Venom via Increase of Death Receptor 3 Expression and Inactivation of NF-kappa B in NSCLC Cells [J].
Choi, Kyung Eun ;
Hwang, Chul Ju ;
Gu, Sun Mi ;
Park, Mi Hee ;
Kim, Joo Hwan ;
Park, Joo Ho ;
Ahn, Young Jin ;
Kim, Ji Young ;
Song, Min Jong ;
Song, Ho Sueb ;
Han, Sang-Bae ;
Hong, Jin Tae .
TOXINS, 2014, 6 (08) :2210-2228
[8]   Adenovirus-mediated expression of TIMP-1 and TIMP-2 in bone inhibits osteolytic degradation by human prostate cancer [J].
Deng, Xiyun ;
He, Guangchun ;
Levine, Andrea ;
Ca, Ya ;
Mullins, Chad .
INTERNATIONAL JOURNAL OF CANCER, 2008, 122 (01) :209-218
[9]  
Dimitroulakos J, 2001, CLIN CANCER RES, V7, P158
[10]   Breast cancer in China [J].
Fan, Lei ;
Strasser-Weippl, Kathrin ;
Li, Jun-Jie ;
St Louis, Jessica ;
Finkelstein, Dianne M. ;
Yu, Ke-Da ;
Chen, Wan-Qing ;
Shao, Zhi-Ming ;
Goss, Paul E. .
LANCET ONCOLOGY, 2014, 15 (07) :E279-E289