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作 者:Song Hu Wei Zhu Ling-Fei Zhang Ming Pei Mo-Fang Liu
机构地区:[1]Center for RNA Research, State Key Laboratory of Molecular Biology, University of Chinese Academy of Sciences, Shanghai 200031, China [2]Shanghai Key Laboratory of Molecular Andrology, Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200031, China [3]Department of General Surgery, Zhongshan Hospital, Fudan University, Shanghai 200032, China [4]Shanghai Qibao High school, Shanghai 201101, China
出 处:《Cell Research》2014年第2期254-257,共4页细胞研究(英文版)
基 金:This work was supported by grants from the Ministry of Science and Technology of China (2011CB811303, 2012CB910802, 2014CB964802) and the National Natural Science Foundation of China (91219306, 31270840, 31170754, 30970621).
摘 要:Dear Editor, During the last decades, a number of key mediators of inflammation-induced tumorigenesis have been identified to support tumor progression in response to inflammation stimulation [1]. Recent studies show that a few cancerrelated microRNAs (miRNAs) are modulated by inflammation signals [2, 3], implicating miRNAs as a new class of mediators between inflammation and cancer. However, how inflammation regulates miRNAs in cancer cells and how such miRNA mediators function in inflammationassociated tumorigenesis remain largely unexplored.
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