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miR-216b suppresses tumor growth and invasion by targeting KRAS in nasopharyngeal carcinoma
Author(s) -
Min Deng,
Hailin Tang,
Yanhong Zhou,
Ming Zhou,
Wei Xiong,
Ying Zheng,
Qiurong Ye,
Xi Zeng,
Qianjin Liao,
Xiaofang Guo,
Xiaoling Li,
Jian Ma,
Guiyuan Li
Publication year - 2011
Publication title -
journal of cell science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.384
H-Index - 278
eISSN - 1477-9137
pISSN - 0021-9533
DOI - 10.1242/jcs.085050
Subject(s) - biology , kras , cancer research , microrna , nasopharyngeal carcinoma , carcinogenesis , cancer , cell growth , colorectal cancer , medicine , gene , radiation therapy , genetics
MicroRNAs (miRNAs) are small noncoding RNAs that are involved in various diseases, including cancer. In the present study, we found that miR-216b was downregulated in nasopharyngeal carcinoma (NPC) cell lines and specimens. Decreased expression of miR-216b was directly related to advanced clinical stage and lymph node metastasis. miR-216b levels correlated inversely with levels of KRAS protein during nasopharyngeal tumorigenesis. Furthermore, we demonstrated that miR-216b can bind to the 3' untranslated region (UTR) of KRAS and inhibit expression of the KRAS protein. Both in vitro and in vivo assays revealed that miR-216b attenuated NPC cell proliferation, invasion and tumor growth in nude mice. miR-216b exerts its tumor suppressor function through inhibition of the KRAS-related AKT and ERK pathways. Our findings provide, for the first time, significant clues regarding the role of miR-216b as a tumor suppressor by targeting KRAS in NPC.

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