神经母细胞瘤微环境、异质性和免疫治疗方法

Cancers Pub Date : 2024-05-13 DOI:10.3390/cancers16101863
Panagiotis Alkinoos Polychronopoulos, O. Bedoya-Reina, J. Johnsen
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摘要

神经母细胞瘤是一种外周神经系统肿瘤,几乎只发生在幼儿身上。尽管强化治疗方法提高了患者的生存率,但高危患者的预后仍在50%左右,这表明神经母细胞瘤是儿童癌症相关死亡的主要原因。神经母细胞瘤是一种胚胎性肿瘤,起源于神经嵴内的细胞。因此,神经母细胞瘤的突变负荷通常较低,大多数情况下是由表观遗传失调的转录网络驱动的。最近 Omic 技术的发展让我们详细了解了神经母细胞瘤的进化、异质性和可塑性,以及神经母细胞瘤微环境中细胞内和细胞间的分子通讯网络。在此,我们将讨论这些最新发现的潜力,重点是新的治疗模式,包括有望改善未来治疗方案的免疫疗法。
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The Neuroblastoma Microenvironment, Heterogeneity and Immunotherapeutic Approaches
Neuroblastoma is a peripheral nervous system tumor that almost exclusively occurs in young children. Although intensified treatment modalities have led to increased patient survival, the prognosis for patients with high-risk disease is still around 50%, signifying neuroblastoma as a leading cause of cancer-related deaths in children. Neuroblastoma is an embryonal tumor and is shaped by its origin from cells within the neural crest. Hence, neuroblastoma usually presents with a low mutational burden and is, in the majority of cases, driven by epigenetically deregulated transcription networks. The recent development of Omic techniques has given us detailed knowledge of neuroblastoma evolution, heterogeneity, and plasticity, as well as intra- and intercellular molecular communication networks within the neuroblastoma microenvironment. Here, we discuss the potential of these recent discoveries with emphasis on new treatment modalities, including immunotherapies which hold promise for better future treatment regimens.
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