UC Davis Medical Center, Sacramento, CA 95817, USA.
Int J Mol Sci. 2024 Oct 12;25(20):10990. doi: 10.3390/ijms252010990.
Many central nervous system (CNS) disorders lack approved treatment options. Previous research demonstrated that peptide CAQK can bind to chondroitin sulfate proteoglycans (CSPGs) in the extracellular matrix of the CNS. In vivo studies have investigated CAQK conjugated to nanoparticles containing therapeutic agents with varying methodologies/outcomes. This paper presents the first systematic review assessing its properties, applications, and outcomes secondary to its use. Following PRISMA guidelines, a comprehensive search was performed across multiple databases. Studies utilizing CAQK as a therapeutic agent/homing molecule in animal/human models were selected. Sixteen studies met the inclusion criteria. Mice and rats were the predominant animal models. All studies except one used CAQK to deliver a therapeutic agent. The reviewed studies mostly included models of brain and spinal cord injuries. Most studies had intravenous administration of CAQK. All studies demonstrated various benefits and that CAQK conjugation facilitated localization to target tissues. No studies directly evaluated the effects of CAQK alone. The data are limited by the heterogeneity in study methodologies and the lack of direct comparison between CAQK and conjugated agents. Overall, these findings present CAQK utilization to deliver a therapeutic agent as a promising targeting strategy in the management of disorders where CSPGs are upregulated.
许多中枢神经系统 (CNS) 疾病缺乏批准的治疗方法。先前的研究表明,肽 CAQK 可以与中枢神经系统细胞外基质中的软骨素硫酸盐蛋白聚糖 (CSPG) 结合。体内研究已经研究了与含有不同方法/结果的治疗剂的纳米颗粒偶联的 CAQK。本文介绍了首次评估其特性、应用和使用后结果的系统评价。根据 PRISMA 指南,在多个数据库中进行了全面搜索。选择了在动物/人类模型中使用 CAQK 作为治疗剂/归巢分子的研究。符合纳入标准的研究有 16 项。小鼠和大鼠是主要的动物模型。除一项研究外,所有研究均使用 CAQK 输送治疗剂。综述的研究大多包括脑和脊髓损伤模型。大多数研究采用 CAQK 的静脉内给药。所有研究均证明了各种益处,并且 CAQK 缀合有助于将药物定位到靶组织。没有研究直接评估 CAQK 单独的效果。这些数据受到研究方法学的异质性以及缺乏 CAQK 与缀合剂之间直接比较的限制。总的来说,这些发现表明,CAQK 作为一种有前途的靶向策略,用于治疗 CSPG 上调的疾病,以输送治疗剂。