Zurita Amado J, Troncoso Patricia, Cardó-Vila Marina, Logothetis Christopher J, Pasqualini Renata, Arap Wadih
Department of Genitourinary Medical Oncology, The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030, USA.
Cancer Res. 2004 Jan 15;64(2):435-9. doi: 10.1158/0008-5472.can-03-2675.
Direct screening of combinatorial peptide libraries in patients may allow the identification of ligands that target biochemical differences in the endothelium of blood vessels. In a screening performed in a patient, we selected and isolated a mimic motif of interleukin 11 (IL-11) from prostate biopsies after an i.v. administration of a phage display peptide library. We also demonstrated that the IL-11 phage mimic (displaying the cyclic nonapeptide CGRRAGGSC) bound specifically to a corresponding IL-11 receptor (IL-11Ralpha). Here we show that IL-11Ralpha is a potential target for intervention in human prostate cancer through morphological and functional analyses. First, a comprehensive serial immunohistochemical analysis of primary and metastatic prostate cancer samples showed increased stage-specific expression of IL-11Ralpha during disease progression. Second, a proapoptotic peptide was specifically targeted and internalized through this functional IL-11Ralpha-based ligand-receptor pair: treatment of prostate cancer cells in vitro with a proapoptotic peptide guided by the CGRRAGGSC peptide to the IL-11Ralpha resulted in dose-dependent apoptosis. Together, these data indicate that the IL-11Ralpha is a candidate target for translational clinical trials against advanced and metastatic prostate cancer. Moreover, our results illustrate the ability of direct combinatorial screening systems in cancer patients for identification of relevant targets in the context of human disease.
在患者中直接筛选组合肽库可能有助于识别靶向血管内皮细胞生化差异的配体。在对一名患者进行的筛选中,我们在静脉注射噬菌体展示肽库后,从前列腺活检组织中选择并分离出白细胞介素11(IL-11)的模拟基序。我们还证明,IL-11噬菌体模拟物(展示环状九肽CGRRAGGSC)能特异性结合相应的IL-11受体(IL-11Rα)。在此,我们通过形态学和功能分析表明,IL-11Rα是干预人类前列腺癌的一个潜在靶点。首先,对原发性和转移性前列腺癌样本进行的全面连续免疫组织化学分析显示,在疾病进展过程中,IL-11Rα的阶段特异性表达增加。其次,一种促凋亡肽通过这种基于功能性IL-11Rα的配体-受体对被特异性靶向并内化:用由CGRRAGGSC肽引导至IL-11Rα的促凋亡肽体外处理前列腺癌细胞会导致剂量依赖性凋亡。总之,这些数据表明,IL-11Rα是针对晚期和转移性前列腺癌进行转化临床试验的候选靶点。此外,我们的结果说明了癌症患者中直接组合筛选系统在人类疾病背景下识别相关靶点的能力。