Juncker-Jensen A, Lykkesfeldt A E, Worm J, Ralfkiaer U, Espelund U, Jepsen J S
Department of Tumor Endocrinology, Institute of Cancer Biology, Danish Cancer Society, Strandboulevarden 49, DK-2100 Copenhagen, Denmark.
Growth Horm IGF Res. 2006 Aug;16(4):224-39. doi: 10.1016/j.ghir.2006.06.005. Epub 2006 Aug 8.
Antiestrogens target the estrogen receptor and counteract the growth stimulatory action of estrogen on human breast cancer. However, acquired resistance to antiestrogens is a major clinical problem in endocrine treatment of breast cancer patients. To mimic acquired resistance, we have used a model system with the antiestrogen sensitive human breast cancer cell line MCF-7 and several antiestrogen resistant cell lines derived from the parental MCF-7 cell line. This model system was used to study the expression and possible involvement in resistant cell growth of insulin-like growth factor binding protein 2 (IGFBP-2). By an oligonucleotide based microarray, we compared the expression of mRNAs encoding insulin-like growth factor binding protein 1,2,3,4,5 and 6 (IGFBP-1 to -6) in the parental MCF-7 cell line to three human breast cancer cell lines, resistant to the antiestrogen ICI 182,780 (Faslodex/Fulvestrant). Only IGFBP-2 mRNA was overexpressed in all three resistant cell lines. Thus, we compared the IGFBP-2 protein expression in MCF-7 cells to nine antiestrogen resistant breast cancer cell lines, resistant to either ICI 182,780 or tamoxifen or RU 58,668 and found that IGFBP-2 was overexpressed in all nine resistant cell lines. Three of the resistant cell lines, resistant to different antiestrogens, were selected for further studies and IGFBP-2 overexpression was demonstrated at the mRNA level as well as the intra- and extracellular protein level. The objective of this study was to examine if IGFBP-2 is involved in growth of antiestrogen resistant human breast cancer cells. Therefore, IGFBP-2 expression was inhibited by antisense oligonucletides and siRNA. Specific inhibition of IGFBP-2 protein expression was achieved in MCF-7 and the three selected antiestrogen resistant cell lines, but no effect on resistant cell growth was observed. Thus, we were able to establish IGFBP-2 as a marker for antiestrogen resistant breast cancer cell lines, although IGFBP-2 was not a major contributor to the resistant cell growth.
抗雌激素药物作用于雌激素受体,可对抗雌激素对人类乳腺癌的生长刺激作用。然而,抗雌激素药物的获得性耐药是乳腺癌患者内分泌治疗中的一个主要临床问题。为模拟获得性耐药,我们使用了一个模型系统,该系统包含抗雌激素敏感的人乳腺癌细胞系MCF-7以及从亲代MCF-7细胞系衍生而来的几种抗雌激素耐药细胞系。此模型系统用于研究胰岛素样生长因子结合蛋白2(IGFBP-2)的表达及其在耐药细胞生长中的可能作用。通过基于寡核苷酸的微阵列,我们比较了亲代MCF-7细胞系中编码胰岛素样生长因子结合蛋白1、2、3、4、5和6(IGFBP-1至-6)的mRNA表达与三种对抗雌激素ICI 182,780(氟维司群/芙仕得)耐药的人乳腺癌细胞系的表达情况。仅IGFBP-2 mRNA在所有三种耐药细胞系中均过度表达。因此,我们比较了MCF-7细胞与九种对ICI 182,780或他莫昔芬或RU 58,668耐药的抗雌激素耐药乳腺癌细胞系中IGFBP-2蛋白的表达,发现IGFBP-2在所有九种耐药细胞系中均过度表达。选择了三种对不同抗雌激素耐药的细胞系进行进一步研究,结果表明IGFBP-2在mRNA水平以及细胞内和细胞外蛋白水平均过度表达。本研究的目的是检验IGFBP-2是否参与抗雌激素耐药的人乳腺癌细胞的生长。因此,采用反义寡核苷酸和小干扰RNA抑制IGFBP-2的表达。在MCF-7细胞和三种选定的抗雌激素耐药细胞系中实现了对IGFBP-2蛋白表达的特异性抑制,但未观察到对耐药细胞生长的影响。因此,我们能够将IGFBP-2确立为抗雌激素耐药乳腺癌细胞系的一个标志物,尽管IGFBP-2并非耐药细胞生长的主要促成因素。