Sainero-Alcolado Lourdes, Sjöberg Bexelius Tomas, Santopolo Giuseppe, Yuan Ye, Liaño-Pons Judit, Arsenian-Henriksson Marie
Department of Microbiology, Tumor and Cell Biology (MTC), Biomedicum B7, Karolinska Institutet, Stockholm SE-17165, Sweden.
Department of Women's and Children's Health, Karolinska Institutet, Stockholm SE-17177, Sweden.
Neuro Oncol. 2024 Dec 5;26(12):2174-2192. doi: 10.1093/neuonc/noae152.
Neuroblastoma (NB), a heterogenous pediatric tumor of the sympathetic nervous system, is the most common and deadly extracranial solid malignancy diagnosed in infants. Numerous efforts have been invested in understanding its origin and in development of novel curative targeted therapies. Here, we summarize the recent advances in the identification of the cell of origin and the genetic alterations occurring during development that contribute to NB. We discuss current treatment regimens, present and future directions for the identification of novel therapeutic metabolic targets, differentiation agents, as well as personalized combinatory therapies as potential approaches for improving the survival and quality of life of children with NB.
神经母细胞瘤(NB)是一种起源于交感神经系统的异质性儿科肿瘤,是婴儿期诊断出的最常见且致命的颅外实体恶性肿瘤。人们已投入大量精力来了解其起源,并致力于开发新型的靶向治愈性疗法。在此,我们总结了在确定其起源细胞以及发育过程中发生的导致NB的基因改变方面的最新进展。我们讨论了当前的治疗方案、鉴定新型治疗性代谢靶点和分化剂的现状与未来方向,以及个性化联合疗法,这些都是提高NB患儿生存率和生活质量的潜在方法。