Catuogno S, Esposito C L, Quintavalle C, Condorelli G, de Franciscis V, Cerchia L
Istituto per l'Endocrinologia e l'Oncologia Sperimentale del CNR "G. Salvatore", Via Pansini 5, 80131 Naples, Italy.
J Signal Transduct. 2012;2012:735135. doi: 10.1155/2012/735135. Epub 2012 May 21.
Gliomas are the most common primary central nervous system tumors with a dismal prognosis. Despite recent advances in surgery, radiotherapy, and chemotherapy, current treatment regimens have a modest survival benefit. A crucial challenge is to deliver drugs effectively to invasive glioma cells residing in a sanctuary within the central nervous system. New therapies are essential, and oligonucleotide-based approaches, including antisense, microRNAs, small interfering RNAs, and nucleic acid aptamers, may provide a viable strategy. Thanks to their unique characteristics (low size, good affinity for the target, no immunogenicity, chemical structures that can be easily modified to improve their in vivo applications), these molecules may represent a valid alternative to antibodies particularly to overcome challenges presented by the blood-brain barrier. Here we will discuss recent results on the use of oligonucleotides that will hopefully provide new effective treatment for gliomas.
胶质瘤是最常见的原发性中枢神经系统肿瘤,预后不佳。尽管最近在手术、放疗和化疗方面取得了进展,但目前的治疗方案对生存期的改善有限。一个关键挑战是将药物有效地递送至位于中枢神经系统“庇护所”内的浸润性胶质瘤细胞。新的治疗方法至关重要,基于寡核苷酸的方法,包括反义核酸、微小RNA、小干扰RNA和核酸适体,可能提供一种可行的策略。由于它们的独特特性(尺寸小、对靶点亲和力高、无免疫原性、化学结构易于修饰以改善其体内应用),这些分子可能是抗体的有效替代物,特别是用于克服血脑屏障带来的挑战。在此,我们将讨论使用寡核苷酸的最新结果,有望为胶质瘤提供新的有效治疗方法。