Pattwell Siobhan S, Konnick Eric Q, Liu Yajuan J, Yoda Rebecca A, Sekhar Laligam N, Cimino Patrick J
Division of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
Department of Laboratory Medicine, University of Washington, Seattle, WA, USA.
Case Rep Pathol. 2020 Jan 30;2020:5903863. doi: 10.1155/2020/5903863. eCollection 2020.
Pilocytic astrocytoma is a low-grade glial neoplasm of the central nervous system (CNS) that tends to occur in the pediatric population and less commonly presents in adults. Hereditary pilocytic astrocytoma is often associated with germline genetic alterations in the tumor suppressor , the gene responsible for the syndrome neurofibromatosis type 1. Sporadic pilocytic astrocytoma frequently harbors somatic alterations in , with rare pilocytic astrocytomas containing alterations in and . encodes for the protein tropomyosin receptor kinase B (TrkB), which is a neurotrophin receptor with high affinity for Brain-Derived Neurotrophic Factor (BDNF), and plays a role in several physiological functions of neurons, including cell survival and differentiation. In this report, we describe a novel gene fusion occurring in an adult sporadic pilocytic astrocytoma and review the biology and implications of specific mutations occurring in CNS neoplasms.
毛细胞型星形细胞瘤是中枢神经系统(CNS)的一种低级别胶质瘤,多见于儿童,成人中较少见。遗传性毛细胞型星形细胞瘤常与肿瘤抑制基因的种系遗传改变有关,该基因是1型神经纤维瘤病综合征的致病基因。散发性毛细胞型星形细胞瘤常存在该基因的体细胞改变,罕见的毛细胞型星形细胞瘤含有该基因及其他基因的改变。该基因编码原肌球蛋白受体激酶B(TrkB)蛋白,TrkB是一种对脑源性神经营养因子(BDNF)具有高亲和力的神经营养因子受体,在神经元的多种生理功能中发挥作用,包括细胞存活和分化。在本报告中,我们描述了一例发生于成人散发性毛细胞型星形细胞瘤中的新型该基因融合,并综述了中枢神经系统肿瘤中特定该基因突变的生物学特性及意义。