Srinivasa Komal, Cross Kevin A, Dahiya Sonika
Department of Pathology & Immunology, Washington University School of Medicine, St. Louis, MO, United States.
Department of Neurosurgery, Washington University School of Medicine, St. Louis, MO, United States.
Front Oncol. 2020 Sep 15;10:574974. doi: 10.3389/fonc.2020.574974. eCollection 2020.
(alternately referred to as v-raf murine sarcoma viral oncogene homolog B1) is a proto-oncogene involved in the mitogen-activated protein kinase () pathway. alterations are most commonly missense mutations or aberrant fusions. These mutations are observed in numerous primary central nervous system tumors as well as metastases. This review discusses the prevalence of alteration within select notable CNS tumors, and their prognostic associations. Included are some novel entities such as diffuse leptomeningeal glioneuronal tumor (DLGNT), polymorphous low grade neuroepithelial tumor of the young (PLNTY), and multinodular and vacuolating neuronal tumor (MVNT). Knowledge of this gene's integrity in CNS and PNS tumors can have profound diagnostic and therapeutic implications. Also reviewed are the current state of targeted therapy against aberrant as it pertains mostly to the CNS and to a lesser extent in PNS, and certain diagnostic aspects.
(也被称为v-raf鼠肉瘤病毒癌基因同源物B1)是一种参与丝裂原活化蛋白激酶()途径的原癌基因。其改变最常见的是错义突变或异常融合。这些突变在许多原发性中枢神经系统肿瘤以及转移瘤中都有观察到。本综述讨论了特定显著中枢神经系统肿瘤中该基因改变的发生率及其预后关联。其中包括一些新的实体,如弥漫性软脑膜神经胶质神经元肿瘤(DLGNT)、青少年多形性低级别神经上皮肿瘤(PLNTY)和多结节空泡状神经元肿瘤(MVNT)。了解该基因在中枢神经系统和周围神经系统肿瘤中的完整性可能具有深远的诊断和治疗意义。还综述了针对异常该基因的靶向治疗的现状,因为它主要涉及中枢神经系统,在周围神经系统中的程度较小,以及某些诊断方面。