Department of Physiology, Tufts University School of Medicine, 136 Harrison Avenue, Boston, MA 02111, USA
Mol Cancer Res. 2011 May;9(5):637-47. doi: 10.1158/1541-7786.MCR-09-0237. Epub 2011 Feb 25.
We developed surface proteome signatures (SPS) for identification of new biomarkers playing a role in cancer drug resistance. SPS compares surface antigen expression of different cell lines by immunocytochemistry of a phage display antibody library directed to surface antigens of HT1080 fibrosarcoma cells. We applied SPS to compare the surface proteomes of two epithelial derived cancer cell lines, MCF7 and NCI/ADR-RES, which is drug resistant because of overexpression of the P-glycoprotein (P-gp) drug efflux pump. Surface proteomic profiling identified CD44 as an additional biomarker that distinguishes between these two cell lines. CD44 immunohistochemistry can distinguish between tumors derived from these lines and predict tumor response to doxorubicin in vivo. We further show that CD44 plays a role in drug resistance, independently of P-gp, in NCI/ADR-RES cells and increases expression of the antiapoptotic protein Bcl-xL. Our findings illustrate the utility of SPS to distinguish between cancer cell lines and their derived tumors and identify novel biomarkers involved in drug resistance.
我们开发了表面蛋白质组特征(SPS),用于鉴定在癌症药物耐药性中起作用的新生物标志物。SPS 通过针对 HT1080 纤维肉瘤细胞表面抗原的噬菌体展示抗体文库对不同细胞系的表面抗原表达进行免疫细胞化学比较。我们应用 SPS 比较了两种上皮来源的癌细胞系 MCF7 和 NCI/ADR-RES 的表面蛋白质组,后者由于 P 糖蛋白(P-gp)药物外排泵的过度表达而具有耐药性。表面蛋白质组学分析鉴定出 CD44 是区分这两种细胞系的另一个生物标志物。CD44 免疫组化可以区分来自这些系的肿瘤,并预测体内多柔比星的肿瘤反应。我们进一步表明,CD44 独立于 P-gp 在 NCI/ADR-RES 细胞中发挥作用,增加了抗凋亡蛋白 Bcl-xL 的表达。我们的研究结果说明了 SPS 在区分癌细胞系及其衍生肿瘤以及鉴定参与耐药性的新生物标志物方面的实用性。