Teng Xin-Qi, Qu Jian, Li Guo-Hua, Zhuang Hai-Hui, Qu Qiang
Department of Pharmacy, Xiangya Hospital, Central South University, Changsha, China.
National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, China.
Front Cell Dev Biol. 2022 Jul 8;10:824299. doi: 10.3389/fcell.2022.824299. eCollection 2022.
Gliomas are central nervous system tumors originating from glial cells, whose incidence and mortality rise in coming years. The current treatment of gliomas is surgery combined with chemotherapy or radiotherapy. However, developing therapeutic resistance is one of the significant challenges. Recent research suggested that small interfering RNA (siRNA) has excellent potential as a therapeutic to silence genes that are significantly involved in the manipulation of gliomas' malignant phenotypes, including proliferation, invasion, metastasis, therapy resistance, and immune escape. However, it is challenging to deliver the naked siRNA to the action site in the cells of target tissues. Therefore, it is urgent to develop delivery strategies to transport siRNA to achieve the optimal silencing effect of the target gene. However, there is no systematic discussion about siRNAs' clinical potential and delivery strategies in gliomas. This review mainly discusses siRNAs' delivery strategies, especially nanotechnology-based delivery systems, as a potential glioma therapy. Moreover, we envisage the future orientation and challenges in translating these findings into clinical applications.
胶质瘤是起源于神经胶质细胞的中枢神经系统肿瘤,其发病率和死亡率在未来几年呈上升趋势。目前胶质瘤的治疗方法是手术联合化疗或放疗。然而,产生治疗抗性是重大挑战之一。最近的研究表明,小干扰RNA(siRNA)作为一种治疗手段,在沉默那些显著参与调控胶质瘤恶性表型(包括增殖、侵袭、转移、治疗抗性和免疫逃逸)的基因方面具有巨大潜力。然而,将裸露的siRNA递送至靶组织细胞中的作用位点具有挑战性。因此,迫切需要开发递送策略来转运siRNA,以实现靶基因的最佳沉默效果。然而,目前尚无关于siRNA在胶质瘤中的临床潜力和递送策略的系统性讨论。本综述主要讨论siRNA的递送策略,尤其是基于纳米技术的递送系统,作为一种潜在的胶质瘤治疗方法。此外,我们设想了将这些研究结果转化为临床应用的未来方向和挑战。