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髓母细胞瘤:从分子亚群到分子靶向治疗。

Medulloblastoma: From Molecular Subgroups to Molecular Targeted Therapies.

机构信息

Tumor Initiation and Maintenance Program, NCI-Designated Cancer Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, California 92037, USA; email:

Division of Haematology/Oncology and Department of Paediatrics, Hospital for Sick Children, Toronto, Ontario M5G 1X8, Canada.

出版信息

Annu Rev Neurosci. 2018 Jul 8;41:207-232. doi: 10.1146/annurev-neuro-070815-013838. Epub 2018 Apr 11.

Abstract

Brain tumors are the leading cause of cancer-related death in children, and medulloblastoma (MB) is the most common malignant pediatric brain tumor. Advances in surgery, radiation, and chemotherapy have improved the survival of MB patients. But despite these advances, 25-30% of patients still die from the disease, and survivors suffer severe long-term side effects from the aggressive therapies they receive. Although MB is often considered a single disease, molecular profiling has revealed a significant degree of heterogeneity, and there is a growing consensus that MB consists of multiple subgroups with distinct driver mutations, cells of origin, and prognosis. Here, we review recent progress in MB research, with a focus on the genes and pathways that drive tumorigenesis, the animal models that have been developed to study tumor biology, and the advances in conventional and targeted therapy.

摘要

脑肿瘤是儿童癌症相关死亡的主要原因,而髓母细胞瘤(MB)是最常见的儿童恶性脑肿瘤。手术、放疗和化疗的进步提高了 MB 患者的生存率。但尽管取得了这些进展,仍有 25-30%的患者死于该疾病,幸存者因接受的强化治疗而遭受严重的长期副作用。尽管 MB 通常被认为是一种单一的疾病,但分子分析揭示了其具有显著的异质性,越来越多的共识认为 MB 由多个具有不同驱动突变、起源细胞和预后的亚组组成。在这里,我们回顾了 MB 研究的最新进展,重点介绍了驱动肿瘤发生的基因和途径、用于研究肿瘤生物学的动物模型以及常规和靶向治疗的进展。

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