miR-20a promotes proliferation and invasion by targeting APP in human ovarian cancer cells

MicroRNAs (miRNAs) are emerging as a class of small regulated RNAs, and the alterations of miRNAs are implicated in the initiation and progression of human cancers. Our study shows that inhibition of miR-20a in OVCAR3 ovarian cancer cell line could suppress, whereas overex- pression of miR-20a could...

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Veröffentlicht in:Acta biochimica et biophysica Sinica 2010-05, Vol.42 (5), p.318-324
Hauptverfasser: Fan, Xingxing, Liu, Yankun, Jiang, Jiechun, Ma, Zhuoya, Wu, Haidong, Liu, Tao, Liu, Min, Li, Xin, Tang, Hua
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Sprache:eng
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Zusammenfassung:MicroRNAs (miRNAs) are emerging as a class of small regulated RNAs, and the alterations of miRNAs are implicated in the initiation and progression of human cancers. Our study shows that inhibition of miR-20a in OVCAR3 ovarian cancer cell line could suppress, whereas overex- pression of miR-20a could enhance cell long-term proliferation and invasion. We also confirmed amyloid precursor protein (APP) as a direct target gene of miR-20a. Furthermore, suppression of APP expression could also promote ovarian cancer cell proliferation and invasion, which is consistent with the results of miR-20a overexpression. Therefore, we concluded that the regulation of APP is an important mechanism for miR-20a to promote proliferation and invasion in ovarian cancer cells.
ISSN:1672-9145
1745-7270
DOI:10.1093/abbs/gmq026