Royal College of Surgeons in Ireland, Dublin, Ireland.
Expert Opin Ther Targets. 2010 Sep;14(9):951-62. doi: 10.1517/14728222.2010.510136.
Neuroblastomas arise from precursor cells of the sympathetic nervous system and are noted for highly heterogeneous clinical behavior. These tumors currently account for approximately 15% of all childhood cancer related deaths in spite of intensive multimodal chemotherapy and are a major problem in pediatric oncology. The identification of novel therapeutic targets is urgently required to reduce patient morbidity.
The purpose of this article is to review and synthesize all of the rapidly expanding evidence for the contribution of microRNAs (miRNAs) in neuroblastoma aggressive disease pathogenesis, along with the prospect of using small RNAs as therapeutics.
The reader will obtain insight on the miRNAs that are dysregulated in neuroblastoma along with potential therapeutic strategies and the most promising targets.
A number of miRNAs which are associated with aggressive disease pathogenesis in neuroblastoma patients have been demonstrated to contribute in major ways to cell proliferation rates, apoptosis, differentiation, invasiveness and tumor growth in vitro and in vivo. Directly or indirectly interfering with the function of these miRNAs may prove to be an important and novel form of therapy.
神经母细胞瘤起源于交感神经系统的前体细胞,并以高度异质性的临床行为为特征。尽管进行了强化的多模式化疗,这些肿瘤目前仍约占所有儿童癌症相关死亡的 15%,并且是儿科肿瘤学的主要问题。迫切需要确定新的治疗靶点,以降低患者的发病率。
本文的目的是回顾和综合所有关于 microRNAs(miRNAs)在神经母细胞瘤侵袭性疾病发病机制中的作用的快速扩展的证据,以及将小 RNA 用作治疗剂的前景。
读者将了解在神经母细胞瘤中失调的 miRNAs 以及潜在的治疗策略和最有前途的靶点。
一些与神经母细胞瘤患者侵袭性疾病发病机制相关的 miRNAs 已被证明在体外和体内对细胞增殖率、细胞凋亡、分化、侵袭性和肿瘤生长有重大影响。直接或间接地干扰这些 miRNAs 的功能可能被证明是一种重要的、新颖的治疗形式。