Concurrent silencing of TBCE and drug delivery to overcome platinum-based resistance in liver cancer

被引:8
|
作者
Li, Senlin [1 ,2 ]
Chen, Siyu [3 ]
Dong, Zhihui [1 ]
Song, Xingdong [2 ]
Li, Xiuling [1 ]
Huang, Ziqi [2 ]
Li, Huiru [2 ]
Huang, Linzhuo [1 ]
Zhuang, Ganyuan [1 ]
Lan, Ran [2 ]
Guo, Mingyan [4 ]
Li, Wende [3 ]
Saw, Phei Er [1 ]
Zhang, Lei [2 ]
机构
[1] Sun Yat Sen Univ, Sun Yat Sen Mem Hosp, Guangdong Prov Key Lab Malignant Tumor Epigenet &, Guangdong Hong Kong Joint Lab RNA Med, Guangzhou 510120, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Sun Yat Sen Mem Hosp, Dept Hepatobiliary Surg, Guangzhou 510120, Peoples R China
[3] Guangdong Lab Anim Monitoring Inst, Guangdong Key Lab Lab Anim, Guangzhou 510663, Peoples R China
[4] Sun Yat Sen Univ, Sun Yat Sen Mem Hosp, Dept Anesthesiol, Guangzhou 510120, Peoples R China
基金
中国国家自然科学基金;
关键词
Hepatocellular carcinoma; Tubulin folding cofactor E; Chemoresistance; siRNA delivery; RNA interference; Nanoparticle; Combination therapy; Nanomedicine; EPITHELIAL-MESENCHYMAL TRANSITION; GROWTH-FACTOR RECEPTOR; HEPATOCELLULAR-CARCINOMA; CISPLATIN; CELLS; SIRNA; ACTIVATION; CHEMORESISTANCE; NANOPARTICLES; THERAPEUTICS;
D O I
10.1016/j.apsb.2022.03.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Platinum-based chemotherapy resistance is a key factor of poor prognosis and recurrence in hepatocellular carcinoma (HCC). Herein, RNAseq analysis revealed that elevated tubulin folding cofactor E (TBCE) expression is associated with platinum-based chemotherapy resistance. High expression of TBCE contributes to worse prognoses and earlier recurrence among liver cancer patients. Mechanisti-cally, TBCE silencing significantly affects cytoskeleton rearrangement, which in turn increases cisplatin-induced cycle arrest and apoptosis. To develop these findings into potential therapeutic drugs, endosomal pH-responsive nanoparticles (NPs) were developed to simultaneously encapsulate TBCE siR-NA and cisplatin (DDP) to reverse this phenomena. NPs (siTBCE + DDP) concurrently silenced TBCE expression, increased cell sensitivity to platinum treatment, and subsequently resulted in superior anti-tumor effects both in vitro and in vivo in orthotopic and patient-derived xenograft (PDX) models. Taken together, NP-mediated delivery and the co-treatment of siTBCE thorn DDP proved to be effective in reversing chemotherapy resistance of DDP in multiple tumor models.(c) 2023 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:967 / 981
页数:15
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