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Suppression of A549 lung cancer cell migration by precursor let-7g microRNA

Cited 13 time in Web of Science Cited 16 time in Scopus
Authors

Park, Sungjin; Minai-Tehrani, Arash; Xu, Cheng-Xiong; Chang, Seung-Hee; Woo, Min-Ah; Noh, Mi-Suk; Lee, Eun-Sun; Lim, Hwang-Tae; An, Gil-Hwan; Lee, Kee-Ho; Sung, Ha-Jung; Beck, George R., Jr.; Cho, Myung-Haing

Issue Date
2010-11
Publisher
Spandidos Publications
Citation
Molecular Medicine Reports, Vol.3 No.6, pp.1007-1013
Abstract
Let-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.
ISSN
1791-2997
URI
https://hdl.handle.net/10371/172473
DOI
https://doi.org/10.3892/mmr.2010.373
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  • College of Veterinary Medicine
  • Department of Veterinary Medicine
Research Area Nanotoxicology, Veterinary Toxicology

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