Patel S, Parkin S M, Bibby M C
Clinical Oncology Unit, University of Bradford, West Yorkshire, UK.
Anticancer Res. 1997 Jan-Feb;17(1A):141-50.
5,6-dimethylxanthenone-4-acetic acid (5,6-MeXAA) is a potent anti-tumour agent which is undergoing early clinical evaluation. It was developed as an improved analogue of flavone acetic acid (FAA) which failed in clinical trial although it had impressive anti-tumour activity in mice. It has been postulated that one possible reason for the clinical failure of FAA was its inability to induce cytokines, especially tumour necrosis factor (TNF) in humans whereas this was seen as an important component of its mechanism of action in mice. Previous studies have demonstrated that 5,6-MeXAA induces mRNA for TNF in the human HL-60 cell line although the protein was not detected. This study has demonstrated mRNA for TNF alpha by RT-PCR in human and murine immune cells incubated with either 5,6-MeXAA, FAA or in culture medium alone. Using a bioassay technique 5,6-MeXAA and FAA were shown to induce TNF production in vitro by murine macrophages but TNF was not detected when human or murine peripheral blood mononuclear cells were stimulated with these agents. A small but significant production of TNF was seen in the HL-60 cell line after 5,6-MeXAA treatment suggesting 5,6-MeXAA can directly stimulate human cells to produce TNF albeit at low levels.
5,6 - 二甲基呫吨酮 - 4 - 乙酸(5,6 - MeXAA)是一种正在进行早期临床评估的强效抗肿瘤药物。它是作为黄酮乙酸(FAA)的改进类似物开发的,FAA在临床试验中失败了,尽管它在小鼠中具有令人印象深刻的抗肿瘤活性。据推测,FAA临床失败的一个可能原因是它无法在人体内诱导细胞因子,特别是肿瘤坏死因子(TNF),而这在小鼠中被视为其作用机制的一个重要组成部分。先前的研究表明,5,6 - MeXAA可在人HL - 60细胞系中诱导TNF的mRNA表达,尽管未检测到蛋白质。本研究通过RT - PCR在与5,6 - MeXAA、FAA或单独培养基孵育的人和小鼠免疫细胞中检测到了TNFα的mRNA。使用生物测定技术表明,5,6 - MeXAA和FAA可在体外诱导小鼠巨噬细胞产生TNF,但当用这些药物刺激人或小鼠外周血单核细胞时未检测到TNF。5,6 - MeXAA处理后,HL - 60细胞系中可见少量但显著的TNF产生,表明5,6 - MeXAA可直接刺激人细胞产生TNF,尽管水平较低。