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作为治疗干预的靶点,肿瘤细胞表面展示的细胞内蛋白可与抗体相关药物结合。

Intracellular proteins displayed on the surface of tumor cells as targets for therapeutic intervention with antibody-related agents.

机构信息

Roche Diagnostics, Division Pharma, Penzberg, Germany.

出版信息

Cancer Genomics Proteomics. 2011 Mar-Apr;8(2):49-63.

Abstract

The identification of targets which are located intracellularly in normal cells and are exposed on the surface of malignant cells is an issue in the target selection process for the development of anticancer agents. Targets with these characteristics should increase the specificity of intervention and the corresponding therapeutic window. We discuss targets such as heat-shock protein 70 (HSP70) and heat-shock protein 90 (HSP90), glucose-regulated protein 78 (GRP78), actin, cytokeratins, vimentin, nucleolin, nucleosomes, estrogen receptor-alpha variant 36 (ER-α36) and feto-acinar pancreatic protein (FAPP). Involvement of these targets in cellular processes, tumor specificity and tractability with antibody-related agents, are discussed.

摘要

在抗癌药物开发的靶标选择过程中,鉴定位于正常细胞内而在恶性细胞表面暴露的靶标是一个问题。具有这些特征的靶标应提高干预的特异性和相应的治疗窗口。我们讨论了热休克蛋白 70(HSP70)和热休克蛋白 90(HSP90)、葡萄糖调节蛋白 78(GRP78)、肌动蛋白、细胞角蛋白、波形蛋白、核仁素、核小体、雌激素受体-α变体 36(ER-α36)和胎胰蛋白(FAPP)等靶标。讨论了这些靶标在细胞过程中的参与、肿瘤特异性和与抗体相关药物的可处理性。

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