Interleukin 6 trigged ataxia-telangiectasia mutated activation facilitates lung cancer metastasis via MMP-3/MMP-13 up-regulation

被引:35
作者
Jiang, Yi Na [1 ]
Yan, Hong Qiong [1 ]
Huang, Xiao Bo [1 ]
Wang, Yi Nan [1 ]
Li, Qing [1 ]
Gao, Feng Guang [1 ,2 ]
机构
[1] Xiamen Univ, Coll Med, Basic Med Sci, Dept Immunol, Xiamen 361005, Peoples R China
[2] Shanghai Jiao Tong Univ, State Key Lab Oncogenes & Related Genes, Shanghai 200032, Peoples R China
基金
中国国家自然科学基金;
关键词
ataxia-telangiectasia mutated; interleukin; 6; lung cancer; metastasis; matrix metalloproteinases; EPITHELIAL-MESENCHYMAL TRANSITION; HEPATOCELLULAR-CARCINOMA; MATRIX METALLOPROTEINASE-13; DOWN-REGULATION; CELL-MIGRATION; COLORECTAL-CANCER; PANCREATIC-CANCER; SIGNALING PATHWAY; B PATHWAY; TGF-BETA;
D O I
10.18632/oncotarget.5825
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Our previous studies show that the phosphorylation of ataxia-telangiectasia mutated (ATM) induced by interleukin 6 (IL-6) treatment contributes to multidrug resistance formation in lung cancer cells, but the exact role of ATM activation in IL-6 increased metastasis is still elusive. In the present study, matrix metalloproteinase-3 (MMP-3) and MMP-13 were firstly demonstrated to be involved in IL-6 correlated cell migration. Secondly, IL-6 treatment not only increased MMP3/MMP-13 expression but also augmented its activities. Thirdly, the inhibition of ATM phosphorylation efficiently abolished IL-6 up-regulating MMP-3/MMP-13 expression and increasing abilities of cell migration. Most importantly, the in vivo test showed that the inhibition of ATM abrogate the effect of IL-6 on lung cancer metastasis via MMP-3/MMP-13 down-regulation. Taken together, these findings demonstrate that IL-6 inducing ATM phosphorylation increases the expression of MMP-3/MMP-13, augments the abilities of cell migration, and promotes lung cancer metastasis, indicating that ATM is a potential target molecule to overcome IL-6 correlated lung cancer metastasis.
引用
收藏
页码:40719 / 40733
页数:15
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