Gadd Samantha L, Hobbs Gerry, Miller Michael R
Department of Biochemistry and Molecular Pharmacology, West Virginia University, Morgantown, West Virginia 26506-9142, USA.
Toxicol Sci. 2002 Apr;66(2):233-43. doi: 10.1093/toxsci/66.2.233.
Studies reported here tested the hypothesis that acetaminophen stimulates proliferation of E2-responsive cells by inducing expression of E2-regulated genes. Ribonuclease protection assays compared the effects of acetaminophen and E2 on expression of selected genes (c-myc, c-fos, cyclin D1, bcl-2, bax, gadd45, mcl-1, p53, p21(CIP1/WAF1), and bcl-xL) in E2-responsive breast cancer (MCF-7) and endometrial adenocarcinoma (Ishikawa) cells as well as in E2-nonresponsive (MDA-MB-231) breast cancer cells. Acetaminophen and E2 increased c-myc RNA levels in MCF-7 cells, consistent with a mitogenic activity of these compounds in MCF-7 cells. However, the magnitude and time course of acetaminophen and E2 induction of c-myc differed. Neither acetaminophen nor E2 induced c-myc in MDA-MB-231 cells, whereas E2, but not acetaminophen, weakly induced c-myc expression in Ishikawa cells. Furthermore, in these 3 cell types, the expression patterns of the other genes differed dramatically in response to acetaminophen and to E2, indicating that acetaminophen does not activate ER as a transcription factor in the same manner as does E2. Additionally, gel shift assays demonstrated that in MCF-7 cells, acetaminophen increased NF-kappaB activity approximately 40% and did not alter AP-1 activity, whereas E2 increased AP-1 activity approximately 50% and did not increase NF-B activity. These studies indicate that acetaminophen effects on gene expression and cell proliferation depend more on cell type/context than on the presence of ER.
对乙酰氨基酚通过诱导雌激素(E2)调控基因的表达来刺激E2反应性细胞的增殖。核糖核酸酶保护分析比较了对乙酰氨基酚和E2对E2反应性乳腺癌(MCF-7)和子宫内膜腺癌(Ishikawa)细胞以及E2无反应性(MDA-MB-231)乳腺癌细胞中所选基因(c-myc、c-fos、细胞周期蛋白D1、bcl-2、bax、gadd45、mcl-1、p53、p21(CIP1/WAF1)和bcl-xL)表达的影响。对乙酰氨基酚和E2增加了MCF-7细胞中c-myc RNA水平,这与这些化合物在MCF-7细胞中的促有丝分裂活性一致。然而,对乙酰氨基酚和E2诱导c-myc的程度和时间进程有所不同。对乙酰氨基酚和E2均未在MDA-MB-231细胞中诱导c-myc,而E2(而非对乙酰氨基酚)在Ishikawa细胞中微弱诱导c-myc表达。此外,在这三种细胞类型中,其他基因对乙酰氨基酚和E2的反应表达模式差异显著,表明对乙酰氨基酚不像E2那样以相同方式激活雌激素受体(ER)作为转录因子。另外,凝胶迁移试验表明,在MCF-7细胞中,对乙酰氨基酚使核因子κB(NF-κB)活性增加约40%,且未改变激活蛋白-1(AP-1)活性,而E2使AP-1活性增加约50%,且未增加NF-κB活性。这些研究表明,对乙酰氨基酚对基因表达和细胞增殖的影响更多地取决于细胞类型/环境,而非ER的存在。