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靶向人表皮生长因子受体2(HER2)表位

Targeting HER2 Epitopes.

作者信息

Pal Sumanta Kumar, Pegram Mark

机构信息

Division of Hematology-Oncology, Department of Medicine, David Geffen UCLA School of Medicine, Los Angeles, CA 90095, USA.

出版信息

Semin Oncol. 2006 Aug;33(4):386-91. doi: 10.1053/j.seminoncol.2006.04.004.

Abstract

Variable expression of the HER2 receptor has been implicated in the pathogenesis of a number of malignancies. Many therapeutic modalities have been devised that target the receptor and downstream molecular pathways. The humanized monoclonal antibodies trastuzumab and pertuzumab bind epitopes on the extracellular domain, resulting in cell growth inhibition though a number of proposed mechanisms. Peptidomimetic agents represent short amino acid sequences containing structural features of the antibody complementarity determining regions (CDRs), and appear to have similar inhibitory properties in experimental models. RNA aptamers are ribonucleotide sequences that also exhibit complementarity with extracellular epitopes and lead to growth inhibition. Recent data suggest a synergistic interaction of HER2 epitope-targeting agents when used in combination.

摘要

HER2受体的可变表达与多种恶性肿瘤的发病机制有关。已经设计出许多针对该受体和下游分子途径的治疗方法。人源化单克隆抗体曲妥珠单抗和帕妥珠单抗结合细胞外结构域上的表位,通过多种提出的机制导致细胞生长抑制。拟肽剂代表含有抗体互补决定区(CDR)结构特征的短氨基酸序列,并且在实验模型中似乎具有相似的抑制特性。RNA适体是也与细胞外表位表现出互补性并导致生长抑制的核糖核苷酸序列。最近的数据表明,HER2表位靶向剂联合使用时存在协同相互作用。

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