Institute of Pathology and Molecular Diagnostics, University Clinic Augsburg, Germany.
II. Medical Clinic, University Clinic Augsburg, Germany.
Pathol Res Pract. 2019 Oct;215(10):152572. doi: 10.1016/j.prp.2019.152572. Epub 2019 Aug 1.
The neurotrophic tyrosine receptor kinases (NTRK) play an important role in the development and function of the nervous system. Fusions involving NTRK and a wide range of genes that act as fusion partners are oncogenic and activate well-known signal transduction pathways like the MAPK-ERK pathway. NTRK fusions occur in many very different tumor entities in children and youth as well as in adults. There are a few tumors like secretory breast cancer and congenital fibrosarcoma for which NTRK fusions are pathognomonic. At the same time there a large number of tumors in which NTRK fusions occur in very rare frequency (e.g., lung cancer). TRK inhibitors offer now the possibility to use NTRK fusion as antitumorigenic targets in a tumor agnostic fashion regardless of the basic histology. It is the task of modern pathology to identify such targetable fusions in a highly effective and efficient manner.
神经酪氨酸受体激酶(NTRK)在神经系统的发育和功能中发挥着重要作用。涉及 NTRK 与广泛的作为融合伙伴的基因的融合是致癌的,并激活众所周知的信号转导途径,如 MAPK-ERK 途径。NTRK 融合发生在儿童和青少年以及成人的许多非常不同的肿瘤实体中。有一些肿瘤,如分泌性乳腺癌和先天性纤维肉瘤,其 NTRK 融合是特征性的。同时,有大量的肿瘤中 NTRK 融合发生的频率非常低(例如,肺癌)。TRK 抑制剂现在提供了一种可能,即无论基本组织学如何,以肿瘤不可知的方式将 NTRK 融合作为抗肿瘤靶点。现代病理学的任务是以高效和有效的方式识别这种可靶向的融合。