Okamoto Y, Nakano H
Department of Clinico-Laboratory Diagnostics, Nara Medical University, Japan.
Anticancer Res. 1999 Nov-Dec;19(6B):5175-80.
The effects of dibutyryl cyclic AMP (DBcAMP) on tissue inhibitor metalloproteinase (TIMP) expression were studied in the human hepatoma cell line PLC/PRF/5 with relation to the invasive activity of the cells. Messenger RNA expression levels of metalloproteinases (MMP)-2 and 9, and TIMP-1, 2 and 3 in the cells were determined by semi-quantitative reverse transcription polymerase chain reaction (RT-PCR). MMP-9 and TIMP-2 mRNA expression were not detectable in the cells with or without DBcAMP treatment. Relative MMP-2 and TIMP-1 mRNA expression levels in the cells were not affected by DBcAMP, whereas TIMP-3 mRNA expression was enhanced by DBcAMP. This stimulatory effect of DBcAMP on TIMP-3 expression was confirmed at the mRNA and intracellular protein levels by Northern and Western blotting, respectively. Invasive activity of PLC/PRF/5 cells was determined using the in vitro Matrigel (extracellular matrix extract) invasion model. DBcAMP inhibited the invasive activity of the cells, and this effect was eliminated by addition of an antisense oligonucleotides corresponding to TIMP-3 mRNA. These results suggested that TIMP-3 expression is enhanced by DBcAMP and may play a role in inhibition of the invasive activity of hepatoma cells.
研究了二丁酰环磷腺苷(DBcAMP)对人肝癌细胞系PLC/PRF/5中组织金属蛋白酶抑制剂(TIMP)表达的影响及其与细胞侵袭活性的关系。通过半定量逆转录聚合酶链反应(RT-PCR)测定细胞中金属蛋白酶(MMP)-2、9以及TIMP-1、2和3的信使核糖核酸(mRNA)表达水平。无论有无DBcAMP处理,细胞中均未检测到MMP-9和TIMP-2 mRNA表达。细胞中相对MMP-2和TIMP-1 mRNA表达水平不受DBcAMP影响,而TIMP-3 mRNA表达则被DBcAMP增强。分别通过Northern印迹和Western印迹在mRNA和细胞内蛋白质水平证实了DBcAMP对TIMP-3表达的这种刺激作用。使用体外基质胶(细胞外基质提取物)侵袭模型测定PLC/PRF/5细胞的侵袭活性。DBcAMP抑制细胞的侵袭活性,并且通过添加与TIMP-3 mRNA对应的反义寡核苷酸可消除这种作用。这些结果表明,DBcAMP可增强TIMP-3表达,并且可能在抑制肝癌细胞侵袭活性中发挥作用。