Klotho inhibits growth and promotes apoptosis in human lung cancer cell line A549

被引:94
作者
Chen, Bo [1 ]
Wang, Xueli [1 ]
Zhao, Weihong [1 ]
Wu, Jianqing [1 ]
机构
[1] Nanjing Med Univ, Dept Geriatr, Affiliated Hosp 1, Nanjing 210029, Jiangsu, Peoples R China
来源
JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH | 2010年 / 29卷
基金
中国国家自然科学基金;
关键词
TRANSCRIPTS ENCODING MEMBRANE; FACTOR-I RECEPTOR; BREAST-CANCER; GENE; PATHWAY; PROTEIN; MOUSE; SENSITIVITY; MODEL; RISK;
D O I
10.1186/1756-9966-29-99
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Klotho, as a new anti-aging gene, can shed into circulation and act as a multi-functional humoral factor that influences multiple biological processes. Recently, published studies suggest that klotho can also serve as a potential tumor suppressor. The aim of this study is to investigate the effects and possible mechanisms of action of klotho in human lung cancer cell line A549. Methods: In this study, plasmids encoding klotho or klotho specific shRNAs were constructed to overexpress or knockdown klotho in vitro. A549 cells were respectively treated with pCMV6-MYC-KL or klotho specific shRNAs. The MTT assay was used to evaluate the cytotoxic effects of klotho and flow cytometry was utilized to observe and detect the apoptosis of A549 cells induced by klotho. The activation of IGF-1/insulin signal pathways in A549 cells treated by pCMV6-MYC-KL or shRNAs were evaluated by western blotting. The expression levels of bcl-2 and bax transcripts were evaluated by quantitative reverse transcription-polymerase chain reaction (qRT-PCR). Results: Overexpression of klotho reduced the proliferation of lung cancer A549 cells, whereas klotho silencing in A549 cells enhanced proliferation. Klotho did not show any effects on HEK-293 cells. Klotho overexpression in A549 cells was associated with reduced IGF-1/insulin-induced phosphorylation of IGF-1R (IGF-1 receptor)/IR (insulin receptor) (P < 0.01). Overexpression of klotho can promote the apoptosis of A549 cells (P < 0.01). Overexpression of klotho, a bcl family gene bax, was found up-regulated and bcl-2, an anti-apoptosis gene, was found down-regulated (P < 0.01). In contrast, bax and bcl-2 were found down-regulated (P < 0.05) and up-regulated (P < 0.01), respectively when silencing klotho using shRNAs. Conclusions: Klotho can inhibit proliferation and increase apoptosis of A549 cells, this may be partly due to the inhibition of IGF-1/insulin pathways and involving regulating the expression of the apoptosis-related genes bax/bcl-2. Thus, klotho can serve as a potential tumor suppressor in A549 cells.
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页数:7
相关论文
共 26 条
[1]   Klotho RNAi induces premature senescence of human cells via a p53/p21 dependent pathway [J].
de Oliveira, Rita Machado .
FEBS LETTERS, 2006, 580 (24) :5753-5758
[2]   Down-regulation of IGF-IR using small, interfering, hairpin RNA (siRNA) inhibits growth of human lung cancer cell line A549 in vitro and in nude mice [J].
Dong, Ai-Qiang ;
Kong, Min-Han ;
Ma, Zhi-Yuan ;
Qian, Jian-Fang ;
Xu, Xiao-Hong .
CELL BIOLOGY INTERNATIONAL, 2007, 31 (05) :500-507
[3]   Apoptosis meets signal transduction: Elimination of a BAD influence [J].
Gajewski, TF ;
Thompson, CB .
CELL, 1996, 87 (04) :589-592
[4]   The biochemistry of apoptosis [J].
Hengartner, MO .
NATURE, 2000, 407 (6805) :770-776
[5]   Blocking insulin-like growth factor-I receptor as a strategy for targeting cancer [J].
Hofmann, F ;
García-Echeverría, C .
DRUG DISCOVERY TODAY, 2005, 10 (15) :1041-1047
[6]   Secreted Klotho protein in sera and CSF: implication for post-translational cleavage in release of Klotho protein from cell membrane [J].
Imura, A ;
Iwano, A ;
Tohyama, O ;
Tsuji, Y ;
Nozaki, K ;
Hashimoto, N ;
Fujimori, T ;
Nabeshima, Y .
FEBS LETTERS, 2004, 565 (1-3) :143-147
[7]  
Jemal A, 2009, CA-CANCER J CLIN, V59, P225, DOI [10.3322/caac.20006, 10.3322/caac.21387]
[8]   Mutation of the mouse klotho gene leads to a syndrome resembling ageing [J].
Kuroo, M ;
Matsumura, Y ;
Aizawa, H ;
Kawaguchi, H ;
Suga, T ;
Utsugi, T ;
Ohyama, Y ;
Kurabayashi, M ;
Kaname, T ;
Kume, E ;
Iwasaki, H ;
Iida, A ;
ShirakiIida, T ;
Nishikawa, S ;
Nagai, R ;
Nabeshima, Y .
NATURE, 1997, 390 (6655) :45-51
[9]   Suppression of aging in mice by the hormone Klotho [J].
Kurosu, H ;
Yamamoto, M ;
Clark, JD ;
Pastor, JV ;
Nandi, A ;
Gurnani, P ;
McGuinness, OP ;
Chikuda, H ;
Yamaguchi, M ;
Kawaguchi, H ;
Shimomura, I ;
Takayama, Y ;
Herz, J ;
Kahn, CR ;
Rosenblatt, KP ;
Kuro-o, M .
SCIENCE, 2005, 309 (5742) :1829-1833
[10]   Augmented Wnt signaling in a mammalian model of accelerated aging [J].
Liu, Hongjun ;
Fergusson, Maria M. ;
Castilho, Rogerio M. ;
Liu, Jie ;
Cao, Liu ;
Chen, Jichun ;
Malide, Daniela ;
Rovira, Ilsa I. ;
Schimel, Daniel ;
Kuo, Calvin J. ;
Gutkind, J. Silvio ;
Hwang, Paul M. ;
Finkel, Toren .
SCIENCE, 2007, 317 (5839) :803-806