Down-regulation of microRNA-144 in air pollution-related lung cancer

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作者
Hong-Li Pan
Zhe-Sheng Wen
Yun-Chao Huang
Xin Cheng
Gui-Zhen Wang
Yong-Chun Zhou
Zai-Yong Wang
Yong-Qing Guo
Yi Cao
Guang-Biao Zhou
机构
[1] Chinese Academy of Sciences & Graduate School of the University of Chinese Academy of Sciences,State Key Laboratory of Membrane Biology, Institute of Zoology
[2] the Cancer Hospital,Department of Thoracic Surgery
[3] Sun Yat-Sen University,Department of Thoracic Surgery
[4] the Third Affiliated Hospital of Kunming Medical University (Yunnan Tumor Hospital),Department of Thoracic Surgery
[5] China-Japan Friendship Hospital,Laboratory of Molecular and Experimental Pathology, Kunming Institute of Zoology
[6] Chinese Academy of Sciences,undefined
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Air pollution has been classified as a group 1 carcinogen in humans, but the underlying tumourigenic mechanisms remain unclear. In Xuanwei city of Yunnan Province, the lung cancer incidence is among the highest in China, owing to severe air pollution generated by the combustion of smoky coal, providing a unique opportunity to dissect lung carcinogenesis. To identify abnormal miRNAs critical for air pollution-related tumourigenesis, we performed microRNA microarray analysis in 6 Xuanwei non-small cell lung cancers (NSCLCs) and 4 NSCLCs from control regions where smoky coal was not used. We found 13 down-regulated and 2 up-regulated miRNAs in Xuanwei NSCLCs. Among them, miR-144 was one of the most significantly down-regulated miRNAs. The expanded experiments showed that miR-144 was down-regulated in 45/51 (88.2%) Xuanwei NSCLCs and 34/54 (63%) control region NSCLCs (p = 0.016). MiR-144 interacted with the oncogene Zeb1 at 2 sites in its 3′ untranslated region and a decrease in miR-144 resulted in increased Zeb1 expression and an epithelial mesenchymal transition phenotype. Ectopic expression of miR-144 suppressed NSCLCs in vitro and in vivo by targeting Zeb1. These results indicate that down-regulation of miR-144 is critical for air pollution-related lung cancer and the miR-144-Zeb1 signalling pathway could represent a potential therapeutic target.
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