Levenson A S, Tonetti D A, Jordan V C
Robert H Lurie Cancer Centre, Northwestern University Medical School, Chicago, IL 60611, USA.
Br J Cancer. 1998 Jun;77(11):1812-9. doi: 10.1038/bjc.1998.301.
Oestrogens and antioestrogens modulate the synthesis of transforming growth factor alpha (TGF-alpha) in breast cancer cells. The purpose of the present report was to examine regulation of TGF-alpha gene expression by oestradiol (E2) and antioestrogens in MDA-MB-231 breast cancer cells transfected with either the wild-type or mutant oestrogen receptor (ER). We recently reported the concentration-dependent E2 stimulation of TGF-alpha mRNA in MDA-MB-231 ER transfectants (Levenson et al, 1997). We now report that 4-hydroxytamoxifen (4-OHT) shows oestrogen-like effects on the induction of TGF-alpha gene expression in our transfectants. Accumulation of TGF-alpha mRNA in response to both E2 and 4-OHT but not in response to the pure antioestrogen ICI 182,780 suggests that E2-ER and 4-OHT-ER complexes can bind to an oestrogen response element (ERE), located in the promoter region of the TGF-alpha gene and can activate transcription of the gene. Surprisingly, no activation of luciferase expression was observed after transient transfection of the TGF-alpha ERE/luciferase reporter constructs. Possible activation of an alternative ER-mediated pathway responsible for the regulation of TGF-alpha gene expression in the ER transfectants is discussed.
雌激素和抗雌激素可调节乳腺癌细胞中转化生长因子α(TGF-α)的合成。本报告的目的是研究雌二醇(E2)和抗雌激素对转染野生型或突变型雌激素受体(ER)的MDA-MB-231乳腺癌细胞中TGF-α基因表达的调控。我们最近报道了在MDA-MB-231 ER转染细胞中E2对TGF-α mRNA的浓度依赖性刺激(Levenson等人,1997年)。我们现在报告,4-羟基他莫昔芬(4-OHT)在我们的转染细胞中对TGF-α基因表达的诱导显示出雌激素样作用。TGF-α mRNA对E2和4-OHT均有累积反应,但对纯抗雌激素ICI 182,780无反应,这表明E2-ER和4-OHT-ER复合物可以结合到位于TGF-α基因启动子区域的雌激素反应元件(ERE)上,并可以激活该基因的转录。令人惊讶的是,在瞬时转染TGF-α ERE/荧光素酶报告构建体后未观察到荧光素酶表达的激活。讨论了可能激活负责ER转染细胞中TGF-α基因表达调控的另一种ER介导途径。