Glienke Wolfgang, Maute Luise, Wicht Johannes, Bergmann Lothar
Department of Medicine II (Hämatologie/Onkologie), University Hospital, Johann Wolfgang Goethe-University, Frankfurt am Main, Germany.
Eur J Cancer. 2009 Mar;45(5):874-80. doi: 10.1016/j.ejca.2008.12.030. Epub 2009 Feb 3.
The transcription factor WT1 plays an important role in cellular proliferation and survival of various cancer cells, and is frequently expressed in pancreatic cancer. Curcumin has been shown to be a potentially effective agent in pancreatic cancer. In this context, the purpose of this study was to determine the role of WT1 in a curcumin-treated pancreatic cancer cell line. To study the effect of curcumin on the expression of WT1, we incubated the pancreatic cancer cell line PANC-1 with different amounts of curcumin. The expression of WT1 on mRNA and protein level was measured with real-time RT-PCR and Western blot analysis. The incubation of the pancreatic cancer cell line PANC-1 with curcumin resulted in an inhibition of cellular proliferation as measured with MTT assay. The expression of WT1 on mRNA and protein level was significantly down-regulated in a concentration-dependent manner after treatment with curcumin. The WT1 mRNA levels were decreased by 20%, 25%, 40%, 78% and 88% in response to 10, 20, 30, 40 and 50 microM curcumin. The use of small inhibitory RNA (siRNA) targeting WT1 down-regulated the expression of WT1 about 90%. Combined treatment with curcumin and siRNA targeting WT1 resulted in a significant inhibition of cell proliferation compared to curcumin-treated cells alone. In conclusion, WT1 is involved in cellular proliferation of PANC-1 cells. Targeting WT1 gene expression with siRNA may enhance the efficacy of curcumin to inhibit cell proliferation.
转录因子WT1在多种癌细胞的细胞增殖和存活中起着重要作用,且在胰腺癌中经常表达。姜黄素已被证明是一种对胰腺癌有潜在疗效的药物。在此背景下,本研究的目的是确定WT1在姜黄素处理的胰腺癌细胞系中的作用。为了研究姜黄素对WT1表达的影响,我们用不同剂量的姜黄素处理胰腺癌细胞系PANC-1。通过实时逆转录聚合酶链反应(RT-PCR)和蛋白质印迹分析来检测WT1在mRNA和蛋白质水平的表达。用MTT法检测,用姜黄素处理胰腺癌细胞系PANC-1会导致细胞增殖受到抑制。用姜黄素处理后,WT1在mRNA和蛋白质水平的表达均以浓度依赖的方式显著下调。在分别用10、20、30、40和50微摩尔姜黄素处理后,WT1的mRNA水平分别下降了20%、25%、40%、78%和88%。使用靶向WT1的小干扰RNA(siRNA)可使WT1的表达下调约90%。与单独用姜黄素处理的细胞相比,联合使用姜黄素和靶向WT1的siRNA可显著抑制细胞增殖。总之,WT1参与了PANC-1细胞的细胞增殖。用siRNA靶向WT1基因表达可能会增强姜黄素抑制细胞增殖的疗效。