Kurebayashi J, Otsuki T, Yamamoto S, Kurosumi M, Nakata T, Akinaga S, Sonoo H
Department of Breast and Thyroid Surgery, Okayama, Japan.
Oncology. 1998 Dec;55 Suppl 1:23-34. doi: 10.1159/000055256.
The critical mechanisms responsible for antiestrogen resistance have not yet been elucidated. We previously established a breast cancer cell line, KPL-1, derived from a patient with recurrent disease which appeared under tamoxifenadministration. In a previous study, we suggested that this cell line is estrogen receptor (ER)-positive but tamoxifen-resistant. In the present study, the effects of a pure antiestrogen, ICI 182,780, on this cell line were investigated. Although tamoxifen inhibited neither cell growth nor estradiol-stimulated transcriptional activity in vitro, ICI 182,780, significantly inhibited both of them. Tamoxifen and ICI 182,780 were then administered to female nude mice bearing KPL-1 tumors. Tamoxifen had no effect on tumor growth, but ICI 182,780 unexpectedly stimulated it (p = 0.022). Estradiol tended to inhibit tumor growth (p = 0.198). Immunohistochemical analysis revealed that ICI 182,780 significantly increased the Ki6-labeling index (p<0.001) but estradiol decreased it (p = 0.035). To explore the possible mechanisms of these phenotypes, the mRNA levels of ER-alpha,ER-beta, transforming growth factor-beta1, fibroblast growth factor (FGF)-1 and FGF-4 in KPL-1 cells were compared with those in other ER-positive human breast cancer cell lines by reverse-transcription polymerase chain reaction. FGF-1 was overexpressed only in KPL-1 cells. This cell line is the first breast cancer cell line to be growth-stimulated by ICI 182,780 in vivo. Paracrine interaction between tumor cells and stromal cells mediated by growth factors, such as FGF-1, might be a key factor to explain the unique hormone responsiveness of KPL-1 cells.
导致抗雌激素耐药的关键机制尚未阐明。我们之前建立了一种乳腺癌细胞系KPL-1,它源自一名在服用他莫昔芬期间出现复发性疾病的患者。在之前的一项研究中,我们表明该细胞系雌激素受体(ER)呈阳性但对他莫昔芬耐药。在本研究中,我们研究了一种纯抗雌激素药物ICI 182,780对该细胞系的作用。尽管他莫昔芬在体外既不抑制细胞生长也不抑制雌二醇刺激的转录活性,但ICI 182,780却能显著抑制这两者。然后将他莫昔芬和ICI 182,780给予携带KPL-1肿瘤的雌性裸鼠。他莫昔芬对肿瘤生长没有影响,但ICI 182,780却意外地刺激了肿瘤生长(p = 0.022)。雌二醇倾向于抑制肿瘤生长(p = 0.198)。免疫组织化学分析显示,ICI 182,780显著增加了Ki6标记指数(p<0.001),而雌二醇则使其降低(p = 0.035)。为了探究这些表型的可能机制,通过逆转录聚合酶链反应将KPL-1细胞中ER-α、ER-β、转化生长因子-β1、成纤维细胞生长因子(FGF)-1和FGF-4的mRNA水平与其他ER阳性人乳腺癌细胞系中的水平进行了比较。FGF-1仅在KPL-1细胞中过表达。该细胞系是首个在体内被ICI 182,780刺激生长的乳腺癌细胞系。由生长因子如FGF-1介导的肿瘤细胞与基质细胞之间的旁分泌相互作用可能是解释KPL-1细胞独特激素反应性的关键因素。