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神经生长因子与酪氨酸激酶受体A作为癌症新的治疗靶点

Nerve growth factor & TrkA as novel therapeutic targets in cancer.

作者信息

Demir Ihsan Ekin, Tieftrunk Elke, Schorn Stephan, Friess Helmut, Ceyhan Güralp O

机构信息

Department of Surgery, Klinikum rechts der Isar, Technische Universität München, 81675 Munich, Germany.

Department of Surgery, Klinikum rechts der Isar, Technische Universität München, 81675 Munich, Germany.

出版信息

Biochim Biophys Acta. 2016 Aug;1866(1):37-50. doi: 10.1016/j.bbcan.2016.05.003. Epub 2016 Jun 2.

Abstract

In the past 20years, nerve growth factor (NGF) and its receptors TrkA & p75NTR were recognized to be overexpressed in the overwhelming majority of human solid cancers. Recent studies discovered the presence of overactive TrkA signaling due to TrkA rearrangements or TrkA fusion products in frequent cancers like colorectal cancer, thyroid cancer, or acute myeloid leukemia. Thus, targeting TrkA/NGF via selective small-molecule-inhibitors or antibodies has gained enormous attention in the drug discovery sector. Clinical studies on the anti-cancer impact of NGF-blocking antibodies are likely to be accelerated after the recent removal of clinical holds on these agents by regulatory authorities. Based on these current developments, the present review provides not only a broad overview of the biological effects of NGF-TrkA-p75NTR on cancer cells and their microenvironment, but also explains why NGF and its receptors are going to evoke major interest as promising therapeutic anti-cancer targets in the coming decade.

摘要

在过去20年里,人们认识到神经生长因子(NGF)及其受体TrkA和p75NTR在绝大多数人类实体癌中过度表达。最近的研究发现,在结直肠癌、甲状腺癌或急性髓系白血病等常见癌症中,由于TrkA重排或TrkA融合产物的存在,TrkA信号传导过度活跃。因此,通过选择性小分子抑制剂或抗体靶向TrkA/NGF在药物研发领域受到了极大关注。在监管机构最近解除对这些药物的临床限制后,关于NGF阻断抗体抗癌作用的临床研究可能会加速。基于这些当前的进展,本综述不仅广泛概述了NGF-TrkA-p75NTR对癌细胞及其微环境的生物学效应,还解释了为什么NGF及其受体在未来十年将作为有前景的治疗性抗癌靶点引起人们的极大兴趣。

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