Luiz Marcela Tavares, Dutra Jessyca Aparecida Paes, Tofani Larissa Bueno, de Araújo Jennifer Thayanne Cavalcante, Di Filippo Leonardo Delello, Marchetti Juliana Maldonado, Chorilli Marlus
School of Pharmaceutical Science of Ribeirao Preto, University of Sao Paulo (USP), Ribeirao Preto 14040-900, Brazil.
School of Pharmaceutical Science, Sao Paulo State University (UNESP), Araraquara 14800-903, Brazil.
Pharmaceutics. 2022 Apr 8;14(4):821. doi: 10.3390/pharmaceutics14040821.
Cancer is the second most frequent cause of death worldwide, with 28.4 million new cases expected for 2040. Despite de advances in the treatment, it remains a challenge because of the tumor heterogenicity and the increase in multidrug resistance mechanisms. Thus, gene therapy has been a potential therapeutic approach owing to its ability to introduce, silence, or change the content of the human genetic code for inhibiting tumor progression, angiogenesis, and metastasis. For the proper delivery of genes to tumor cells, it requires the use of gene vectors for protecting the therapeutic gene and transporting it into cells. Among these vectors, liposomes have been the nonviral vector most used because of their low immunogenicity and low toxicity. Furthermore, this nanosystem can have its surface modified with ligands (e.g., antibodies, peptides, aptamers, folic acid, carbohydrates, and others) that can be recognized with high specificity and affinity by receptor overexpressed in tumor cells, increasing the selective delivery of genes to tumors. In this context, the present review address and discuss the main targeting ligands used to functionalize liposomes for improving gene delivery with potential application in cancer treatment.
癌症是全球第二大常见死因,预计到2040年将有2840万新发病例。尽管治疗方面取得了进展,但由于肿瘤异质性和多药耐药机制的增加,它仍然是一个挑战。因此,基因治疗因其能够引入、沉默或改变人类遗传密码的内容以抑制肿瘤进展、血管生成和转移,而成为一种潜在的治疗方法。为了将基因正确递送至肿瘤细胞,需要使用基因载体来保护治疗性基因并将其转运到细胞中。在这些载体中,脂质体因其低免疫原性和低毒性而成为最常用的非病毒载体。此外,这种纳米系统的表面可以用配体(如抗体、肽、适体、叶酸、碳水化合物等)进行修饰,这些配体可以被肿瘤细胞中过度表达的受体以高特异性和亲和力识别,从而增加基因向肿瘤的选择性递送。在此背景下,本综述阐述并讨论了用于脂质体功能化以改善基因递送的主要靶向配体及其在癌症治疗中的潜在应用。