The Effect of Lentiviral Vector-Mediated RNA Interference Targeting Hypoxia-Inducible Factor 1[alpha] on the Uptake of Fluorodeoxyglucose (18F) in the Human Pancreatic Cancer Cell Line, Patu8988

Hypoxia can stimulate [sup]18F-fluorodeoxyglucose ([sup]18F-FDG) uptake in cultured tumor cells. This study has investigated the effect of lentiviral vector-mediated RNA interference (RNAi) targeting hypoxia-inducible factor 1α (HIF-1α) on the changes in HIF-1 and glucose transporter 1 (Glut-1) expr...

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Veröffentlicht in:Cancer biotherapy & radiopharmaceuticals 2015-05, Vol.30 (4), p.160
Hauptverfasser: Fan, Guanglei, Bo, Jingli, Wan, Renming, Peng, Mingya, Luan, Yufen, Deng, Minbin, Xu, Longbao
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Sprache:eng
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Zusammenfassung:Hypoxia can stimulate [sup]18F-fluorodeoxyglucose ([sup]18F-FDG) uptake in cultured tumor cells. This study has investigated the effect of lentiviral vector-mediated RNA interference (RNAi) targeting hypoxia-inducible factor 1α (HIF-1α) on the changes in HIF-1 and glucose transporter 1 (Glut-1) expression, the cell growth, and the uptake of [sup]18F-FDG in the human pancreatic cancer cell line, Patu8988. Lentiviral RNAi vector targeting the HIF-1α gene (LV-HIF-1αRNAi) was constructed and used to treat cells at various concentrations (25-200 nM). The expression changes of HIF-1α and Glut-1 in hypoxic Patu8988 cells after RNAi treatment were determined using real time reverse transcription-polymerase chain reaction (real-time PCR). The inhibition rate of cell proliferation 48 hours after the addition of 10 μL of different concentrations of LV-HIF-1αRNAi (25-200 nM) was assayed using the MTT method. Meanwhile, the cell uptake of [sup]18F-FDG was also assessed. After RNAi transfection, the relative expression levels of HIF-1α mRNA and Glut-1 under hypoxia were reduced and the relative expression levels of HIF-1α protein also decreased. Compared with the control group, the inhibition rates of cell proliferation under different viral dosages were 5.98%, 15.65%, 26.42%, and 40.81%, respectively, positively correlated with the viral doses (r=0.558, p
ISSN:1084-9785
1557-8852
DOI:10.1089/cbr.2014.1700