Periplocin Inhibits Growth of Lung Cancer in vitro and in vivo by Blocking AKT/ERK Signaling Pathways

被引:50
作者
Lu, Ze J. [1 ,2 ]
Zhou, Yan [1 ,2 ]
Song, Qi [1 ,2 ]
Qin, Zhao [3 ]
Zhang, Hong [3 ]
Zhou, Yong J. [1 ,2 ]
Gou, Lan T. [1 ,2 ]
Yang, Jin L. [1 ,2 ]
Luo, Feng [1 ,2 ]
机构
[1] Sichuan Univ, W China Hosp, State Key Lab Biotherapy, Chengdu 610041, Sichuan Prov, Peoples R China
[2] Sichuan Univ, W China Hosp, Ctr Canc, Chengdu 610041, Sichuan Prov, Peoples R China
[3] Sichuan Normal Univ, Res Inst Plant Applicat & Dev, Chengdu, Peoples R China
基金
中国国家自然科学基金;
关键词
Lung cancer; Periplocin; Antitumor agent; AKT; ERK; CARDIAC-GLYCOSIDES; CELLS; THERAPY; TUMORS; EXPRESSION; CARCINOMA; OUABAIN; FAMILY; ROLES; DEATH;
D O I
10.1159/000322328
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Periplocin is one of cardenolides isolated from cortex periplocae which is used for treatment of rheumatoid arthritis and reinforcement of bones and tendons in traditional medicine. Here, we investigated the antitumor activity of periplocin against lung cancer cells both in vitro and in vivo, and explored its anti-cancer mechanism. Periplocin inhibited the growth of lung cancer cells and induced their apoptosis in time-and dose-dependent manners by cell cycle arrest in G0/G1 phase. Periplocin exhibited anti-tumor activity both in human (A549) and mouse (LL/2) lung cancer xenograft models. Immunohistochemical analysis revealed that intratumoral angiogenesis was significantly suppressed. Furthermore, anti-cancer activity mediated by periplocin was associated with decreased level of phosphorylated AKT and ERK both in vitro and in vivo, which were important for cell growth and survival. Moreover, periplocin induced apoptosis by downregulating Bcl-2 and upregulating Bax, leading to activation of caspase-3 and caspase-9. These findings suggested that periplocin could inhibit the growth of lung cancer both in vitro and in vivo, which could be attributed to the inhibition of proliferation and the induction of apoptosis signaling pathway, such as AKT and ERK. These observations provide further evidence on the anti-tumor effect of periplocin, and it may be of importance to further explore its potential role as a therapeutic agent for cancer. Copyright (C) 2010 S. Karger AG, Basel
引用
收藏
页码:609 / 618
页数:10
相关论文
共 25 条
[1]   Identification of a genetic signature of activated signal transducer and activator of transcription 3 in human tumors [J].
Alvarez, JV ;
Febbo, PG ;
Ramaswamy, S ;
Loda, M ;
Richardson, A ;
Frank, DA .
CANCER RESEARCH, 2005, 65 (12) :5054-5062
[2]   The RSK family of kinases: emerging roles in cellular signalling [J].
Anjum, Rana ;
Blenis, John .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2008, 9 (10) :747-758
[3]   Emerging Role for Members of the Bcl-2 Family in Mitochondrial Morphogenesis [J].
Autret, Arnaud ;
Martin, Seamus J. .
MOLECULAR CELL, 2009, 36 (03) :355-363
[4]   Frequent activation of AKT in non-small cell lung carcinomas and preneoplastic bronchial lesions [J].
Balsara, BR ;
Pei, JM ;
Mitsuuchi, Y ;
Page, R ;
Klein-Szanto, A ;
Wang, H ;
Unger, M ;
Testa, JR .
CARCINOGENESIS, 2004, 25 (11) :2053-2059
[5]   Pro-apoptotic and cytostatic activity of naturally occurring cardenolides [J].
Bloise, Elena ;
Braca, Alessandra ;
De Tommasi, Nunziatina ;
Belisario, Maria Antonietta .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2009, 64 (04) :793-802
[6]   Mitochondrial cell death effectors [J].
Brenner, Dirk ;
Mak, Tak W. .
CURRENT OPINION IN CELL BIOLOGY, 2009, 21 (06) :871-877
[7]  
Du Yan-Yan, 2009, Ai Zheng, V28, P456
[8]   From traditional Chinese medicine to rational cancer therapy [J].
Efferth, Thomas ;
Li, Paul C. H. ;
Konkimalla, Venkata S. Badireenath ;
Kaina, Bernd .
TRENDS IN MOLECULAR MEDICINE, 2007, 13 (08) :353-361
[9]   Apoptosis Pathways and Neuroblastoma Therapy [J].
Fulda, S. .
CURRENT PHARMACEUTICAL DESIGN, 2009, 15 (04) :430-435
[10]   Enhanced cytotoxicity induced by gefitinib and specific inhibitors of the Ras or phosphatidyl inositol-3 kinase pathways in non-small cell lung cancer cells [J].
Janmaat, ML ;
Rodriguez, JA ;
Gallegos-Ruiz, M ;
Kruyt, FAE ;
Giaccone, G .
INTERNATIONAL JOURNAL OF CANCER, 2006, 118 (01) :209-214