Zou Han, Poore Brad, Broniscer Alberto, Pollack Ian F, Hu Baoli
Department of Neurological Surgery, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.
Pediatric Neurosurgery, UPMC Children's Hospital of Pittsburgh, Pittsburgh, PA 15224, USA.
Cancers (Basel). 2020 Mar 10;12(3):643. doi: 10.3390/cancers12030643.
Medulloblastoma, the most common pediatric malignant brain tumor, continues to have a high rate of morbidity and mortality in childhood. Recent advances in cancer genomics, single-cell sequencing, and sophisticated tumor models have revolutionized the characterization and stratification of medulloblastoma. In this review, we discuss heterogeneity associated with four major subgroups of medulloblastoma (WNT, SHH, Group 3, and Group 4) on the molecular and cellular levels, including histological features, genetic and epigenetic alterations, proteomic landscape, cell-of-origin, tumor microenvironment, and therapeutic approaches. The intratumoral molecular heterogeneity and intertumoral cellular diversity clearly underlie the divergent biology and clinical behavior of these lesions and highlight the future role of precision treatment in this devastating brain tumor in children.
髓母细胞瘤是儿童最常见的恶性脑肿瘤,在儿童期的发病率和死亡率仍然很高。癌症基因组学、单细胞测序和先进肿瘤模型的最新进展彻底改变了髓母细胞瘤的特征描述和分层。在这篇综述中,我们从分子和细胞水平讨论了与髓母细胞瘤四个主要亚组(WNT、SHH、3组和4组)相关的异质性,包括组织学特征、遗传和表观遗传改变、蛋白质组学特征、细胞起源、肿瘤微环境和治疗方法。肿瘤内分子异质性和肿瘤间细胞多样性显然是这些病变生物学行为和临床行为差异的基础,并突出了精准治疗在这种儿童毁灭性脑肿瘤中的未来作用。