Curcumin suppresses proliferation and invasion in non-small cell lung cancer by modulation of MTA1-mediated Wnt/β-catenin pathway

被引:70
作者
Lu, Yimin [1 ,2 ]
Wei, Changjiang [3 ]
Xi, Zhaoqing [1 ]
机构
[1] Nanjing Univ Chinese Med, Affiliated Hosp 1, Dept Emergency, Nanjing 210029, Jiangsu, Peoples R China
[2] Jiangsu Univ, Peoples Hosp Kunshan 1, Dept Resp Med, Suzhou 215300, Peoples R China
[3] Shanghai Jiao Tong Univ, Sch Med, Suzhou Kowloon Hosp, Dept Thorac Surg, Suzhou 215021, Peoples R China
关键词
Curcumin; Metastasis-associated protein 1; Non-small cell lung cancer; DEPENDENT PATHWAYS; INHIBITS INVASION; TUMOR-METASTASIS; DOWN-REGULATION; MTA1; GENE; EXPRESSION; APOPTOSIS; ALPHA; STRESS; GROWTH;
D O I
10.1007/s11626-014-9779-5
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Curcumin, a naturally occurring phenolic compound, has a diversity of antitumor activities. It has been previously demonstrated that curcumin can inhibit the invasion and metastasis of tumors through activation of the tumor suppressor DnaJ-like heat shock protein 40 (HLJ1). However, the specific roles and mechanisms of curcumin in regulating the malignant behaviors of non-small cell lung cancer (NSCLC) cells still remain unclear. In this study, we found that curcumin could inhibit the proliferation and invasion of NSCLC cells and induce G0/G1 phase arrest. Metastasis-associated protein 1 (MTA1) overexpression has been detected in a wide variety of aggressive tumors and plays an important role on cell invasion and metastasis. Our results showed that curcumin could effectively inhibit the MTA1 expression of NSCLC cells. Further research on the subsequent mechanism showed that curcumin inhibited the proliferation and invasion of NSCLC cells through MTA1-mediated inactivation of Wnt/beta-catenin pathway. Wnt/beta-catenin signaling was reported to play a critical cooperative role on promoting lung tumorigenesis. Thus, these investigations provided novel insights into the mechanisms of curcumin on inhibition of NSCLC cell growth and invasion and showed potential therapeutic strategies for NSCLC.
引用
收藏
页码:840 / 850
页数:11
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