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免疫肿瘤学中的小分子靶点。

Small-Molecule Targets in Immuno-Oncology.

机构信息

Discovery Sciences, Janssen Research & Development, 1400 McKean Road, P O Box 776, Spring House, PA 19477, USA.

Discovery Sciences, Janssen Research & Development, 1400 McKean Road, P O Box 776, Spring House, PA 19477, USA.

出版信息

Cell Chem Biol. 2017 Sep 21;24(9):1148-1160. doi: 10.1016/j.chembiol.2017.08.019.

Abstract

Advances in understanding the role and molecular mechanisms underlying immune surveillance and control of (pre)malignancies is revolutionizing clinical practice in the treatment of cancer. Presently, multiple biologic drugs targeting the immune checkpoint proteins PD(L)1 or CTLA4 have been approved and/or are in advanced stages of clinical development for many cancers. In addition, combination therapy with these agents and other immunomodulators is being intensively explored with the aim of improving primary response rates or prolonging overall survival. The effectiveness of cancer immunotherapy with biologics is spurring research in alternate approaches including small-molecule-mediated targeting of intracellular pathways modulating the innate and adaptive immune response. This focus of this review is on some of the key intracellular pathways where the development of a small-molecule therapeutic is attractive, tractable, and potentially synergistic with extracellular biologic-mediated immune checkpoint blockade.

摘要

在理解免疫监视和控制(前)恶性肿瘤的作用和分子机制方面的进展正在彻底改变癌症治疗的临床实践。目前,已有多种针对免疫检查点蛋白 PD(L)1 或 CTLA4 的生物药物被批准和/或处于许多癌症的临床开发的高级阶段。此外,正在深入探索这些药物与其他免疫调节剂的联合治疗,目的是提高初始反应率或延长总生存期。生物疗法治疗癌症的有效性正在推动替代性方法的研究,包括小分子介导的靶向调节先天和适应性免疫反应的细胞内途径。本综述的重点是一些关键的细胞内途径,在这些途径中,小分子治疗的开发具有吸引力、可操作性,并且可能与细胞外生物介导的免疫检查点阻断协同作用。

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