miR-93, miR-98, and miR-197 Regulate Expression of Tumor Suppressor Gene FUS1

FUS1 is a tumor suppressor gene located on human chromosome 3p21, and expression of Fus1 protein is highly regulated at various levels, leading to lost or greatly diminished tumor suppressor function in many lung cancers. Here we show that selected microRNAs (miRNA) interact with the 3′-untranslated...

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Veröffentlicht in:Molecular cancer research 2009-08, Vol.7 (8), p.1234-1243
Hauptverfasser: Du, Liqin, Schageman, Jeoffrey J, Subauste, Maria C, Saber, Barbara, Hammond, Scott M, Prudkin, Ludmila, Wistuba, Ignacio I, Ji, Lin, Roth, Jack A, Minna, John D, Pertsemlidis, Alexander
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Sprache:eng
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Zusammenfassung:FUS1 is a tumor suppressor gene located on human chromosome 3p21, and expression of Fus1 protein is highly regulated at various levels, leading to lost or greatly diminished tumor suppressor function in many lung cancers. Here we show that selected microRNAs (miRNA) interact with the 3′-untranslated region (3′UTR) of FUS1 , leading to down-regulation of protein expression. Using computational methods, we first predicted that FUS1 is a target of three miRNAs, miR-93, miR-98, and miR-197, and then showed that exogenous overexpression of these miRNAs inhibited Fus1 protein expression. We then confirmed that the three miRNAs target the 3′UTR region of the FUS1 transcript and that individual deletion of the three miRNA target sites in the FUS1 3′UTR restores the expression level of Fus1 protein. We further found that miR-93 and miR-98 are expressed at higher levels in small-cell lung cancer cell lines (SCLC) than in non–small-cell lung cancer cell lines (NSCLC) and immortalized human bronchial epithelial cells (HBEC), and that miR-197 is expressed at higher levels in both SCLCs and NSCLCs than in HBECs. Finally, we found that elevated miR-93 and miR-197 expression is correlated with reduced Fus1 expression in NSCLC tumor specimens. These results suggest that the three miRNAs are negative regulators of Fus1 expression in lung cancers. (Mol Cancer Res 2009;7(8):1234–43)
ISSN:1541-7786
1557-3125
DOI:10.1158/1541-7786.MCR-08-0507