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- Sungjin Park, Arash Minai-Tehrani, Cheng-Xiong Xu, Seung-Hee Chang, Min-Ah Woo, Mi-Suk Noh, Eun-Sun Lee, Hwang-Tae Lim, Gil-Hwan An, Kee-Ho Lee, Ha-Jung Sung, George R Beck, and Myung-Haing Cho.
- Laboratory of Toxicology, College of Veterinary Medicine, Seoul National University, Seoul 151-742, Korea.
- Mol Med Rep. 2010 Nov 1;3(6):1007-13.
AbstractLet-7g miRNAs, short non-coding RNAs approximately 21 nucleotides long, repress protein translation by binding to the 3'UTR of target mRNAs. Aberrant expression of let-7g is associated with the poor prognosis of lung cancer patients. Compared to normal lung cells, let-7g expression is absent in non-small cell lung cancer (NSCLC) cells. Furthermore, K-Ras and HMGA2 are well known as targets of let-7g. In this study, we evaluated the potential role of precursor (pre)-let-7g in lung cancer cell metastasis, focusing on the two targets of let-7g, HMGA2 and K-Ras. We found that pre-let-7g inhibited the migration of A549 lung cancer cells through HMGA2-mediated E2F1 down-regulation. Thus, our results suggest that pre-let-7g could be used as a suitable target for the suppression of lung cancer cell migration.
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