Multifunctional nanoparticles co-loaded with Adriamycin and MDR-targeting siRNAs for treatment of chemotherapy-resistant esophageal cancer

Journal of Nanobiotechnology

Wei Liu¹  Lei Huang²  Wentao Liu³  Chengshen Zhu³  Shuangshuang Lu⁴  Junyi Feng⁴  Chenglin Zhang⁴  Zhimin Wang⁴  Yaohe Wang⁴  Min Wang⁴  Bin Qin⁴  Xiangyang Zhang⁴ 

[1] Children’s Hospital Affiliated to Zhengzhou University;Inflammations Immunity Research Theme, Translational and Clinical Research Institute, FMS, Newcastle University;School of Material Science and Engineering, Zhengzhou University;Sino-British Research Centre for Molecular Oncology, National Centre for International Research in Cell and Gene Therapy, School of Basic Medical Sciences, Academy of Medical Sciences, Zhengzhou University;

关键词: Tumor targeting;    Chemotherapy;    siRNA;    Multidrug resistance;    Esophageal cancer;   

DOI  :  10.1186/s12951-022-01377-x

来源: DOAJ

【 摘 要 】

Abstract The development of multidrug resistance (MDR) during cancer chemotherapy is a major challenge in current cancer treatment strategies. Numerous molecular mechanisms, including increased drug efflux, evasion of drug-induced apoptosis, and activation of DNA repair mechanisms, can drive chemotherapy resistance. Here we have identified the major vault protein (MVP) and the B-cell lymphoma-2 (BCL2) gene as two potential factors driving MDR in esophageal squamous cell carcinoma (ESCC). We have designed a novel and versatile self-assembling nanoparticle (NP) platform on a multifunctional carboxymethyl chitosan base to simultaneously deliver Adriamycin, and siRNAs targeting MVP and BCL2 (CEAMB NPs), thus reducing drug efflux and promoting apoptosis of esophageal cancer cells. To achieve effective delivery to tumor tissues and inhibit tumor growth in vivo, carboxymethyl chitosan was engineered to contain multiple histidines for enhanced cytosol delivery, cholesterol for improved self-assembly, and epidermal growth factor receptor (EGFR) antibodies to target cancer cells. Our results indicate that these nanoparticles are efficiently synthesized with the desired chemical composition to self-assemble into cargo-containing NPs. Furthermore, we have shown that the synthesized NPs will successfully inhibit cancer cells growth and tumor development when delivered to cultured ESCC cells or to in vivo mouse xenograft models. Our engineered NPs offer a potential novel platform in treating various types of chemotherapy-resistant tumors. Graphical Abstract

【 授权许可】

Unknown