Varshosaz Jaleh, Farzan Maryam
Jaleh Varshosaz, Maryam Farzan, Department of Pharmaceutics, Faculty of Pharmacy and Novel Drug Delivery Systems Research Centre, Isfahan University of Medical Sciences, Isfahan 81746-73461, Iran.
World J Gastroenterol. 2015 Nov 14;21(42):12022-41. doi: 10.3748/wjg.v21.i42.12022.
Hepatocellular carcinoma (HCC) is the 5(th) most common malignancy which is responsible for more than half million annual mortalities; also, it is the third leading cause of cancer related death. Unfavorable systemic side-effects of chemotherapeutic agents and susceptibility to the degradation of small interfering RNAs (siRNAs), which can knock down a specific gene involved in the disease, have hampered their clinical application. So, it could be beneficial to develop an efficient carrier for the stabilization and specific delivery of drugs and siRNA to cells. Targeted nanoparticles have gained considerable attention as an efficient drug and gene delivery system, which is due to their capability in achieving the highest accumulation of cytotoxic agents in tumor tissue, modifiable drug pharmacokinetic- and bio-distribution, improved effectiveness of treatment, and limited side-effects. Recent studies have shed more light on the advantages of novel drug loaded carrier systems vs free drugs. Most of the animal studies have reported improvement in treatment efficacy and survival rate using novel carrier systems. Targeted delivery may be achieved passively or actively. In passive targeting, no ligand as homing device is used, while targeting is achieved by incorporating the therapeutic agent into a macromolecule or nanoparticle that passively reaches the target organ. However, in active targeting, the therapeutic agent or carrier system is conjugated to a tissue or cell-specific receptor which is over-expressed in a special malignancy using a ligand called a homing device. This review covers a broad spectrum of targeted nanoparticles as therapeutic and non-viral siRNA delivery systems, which are developed for enhanced cellular uptake and targeted gene silencing in vitro and in vivo and their characteristics and opportunities for the clinical applications of drugs and therapeutic siRNA are discussed in this article. Asialoglycoprotein receptors, low-density lipoprotein, ganglioside GM1 cell surface ligand, epidermal growth factor receptor receptors, monoclonal antibodies, retinoic acid receptors, integrin receptors targeted by Arg-Gly-Asp peptide, folate, and transferrin receptors are the most widely studied cell surface receptors which are used for the site specific delivery of drugs and siRNA-based therapeutics in HCC and discussed in detail in this article.
肝细胞癌(HCC)是第五大常见恶性肿瘤,每年导致超过50万人死亡;此外,它还是癌症相关死亡的第三大主要原因。化疗药物不利的全身副作用以及小干扰RNA(siRNA)易降解的特性(siRNA可敲低与该疾病相关的特定基因)阻碍了它们的临床应用。因此,开发一种能有效稳定药物并将其特异性递送至细胞的载体可能会带来益处。靶向纳米颗粒作为一种高效的药物和基因递送系统已受到广泛关注,这是因为它们能够使细胞毒性药物在肿瘤组织中实现最高程度的蓄积,可改变药物的药代动力学和生物分布,提高治疗效果,并减少副作用。最近的研究进一步揭示了新型载药系统相对于游离药物的优势。大多数动物研究报告称,使用新型载体系统可提高治疗效果和生存率。靶向递送可通过被动或主动方式实现。在被动靶向中,不使用作为归巢装置的配体,而是通过将治疗剂整合到可被动到达靶器官的大分子或纳米颗粒中来实现靶向。然而,在主动靶向中,治疗剂或载体系统与在特定恶性肿瘤中过度表达的组织或细胞特异性受体结合,使用一种称为归巢装置的配体。本综述涵盖了广泛的靶向纳米颗粒,作为治疗性和非病毒性siRNA递送系统,这些系统旨在增强体外和体内的细胞摄取及靶向基因沉默,并在本文中讨论了它们的特性以及药物和治疗性siRNA临床应用的机会。去唾液酸糖蛋白受体、低密度脂蛋白、神经节苷脂GM1细胞表面配体、表皮生长因子受体、单克隆抗体、视黄酸受体、由精氨酸 - 甘氨酸 - 天冬氨酸肽靶向的整合素受体、叶酸和转铁蛋白受体是研究最为广泛的细胞表面受体,它们被用于在HCC中进行药物和基于siRNA疗法的位点特异性递送,并在本文中进行了详细讨论。