Pancreatic Cancer: Nucleic Acid Drug Discovery and Targeted Therapy

被引:5
|
作者
Dai, Hong [1 ,2 ]
Abdullah, Razack [1 ,3 ]
Wu, Xiaoqiu [1 ,2 ]
Li, Fangfei [1 ,2 ,4 ]
Ma, Yuan [1 ,2 ,4 ]
Lu, Aiping [1 ,2 ,4 ]
Zhang, Ge [1 ,2 ,4 ]
机构
[1] Hong Kong Baptist Univ, Law Sau Fai Inst Adv Translat Med Bone & Joint Dis, Sch Chinese Med, Hong Kong, Peoples R China
[2] Hong Kong Baptist Univ, Inst Integrated Bioinfomed & Translat Sci, Sch Chinese Med, Hong Kong, Peoples R China
[3] Inst Advancement Chinese Med IACM Ltd, Shatin, Hong Kong, Peoples R China
[4] HKBU Inst Res & Continuing Educ, Inst Precis Med & Innovat Drug Discovery, Shenzhen, Peoples R China
基金
国家重点研发计划;
关键词
pancreatic cancer; nucleic acid drugs; targeted therapy; aptamer-drug conjugates; antisense oligonucleotides; small interfering RNAs; SMALL-MOLECULE INHIBITORS; ANTISENSE OLIGONUCLEOTIDES; K-RAS; CELL-PROLIFERATION; TUMOR-GROWTH; DUCTAL ADENOCARCINOMA; INDUCED APOPTOSIS; DELIVERY-SYSTEMS; RNA-INTERFERENCE; PROGRESS REPORT;
D O I
10.3389/fcell.2022.855474
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Pancreatic cancer (PC) is one of the most lethal cancers with an almost 10% 5-year survival rate. Because PC is implicated in high heterogeneity, desmoplastic tumor-microenvironment, and inefficient drug-penetration, the chemotherapeutic strategy currently recommended for the treatment of PC has limited clinical benefit. Nucleic acid-based targeting therapies have become strong competitors in the realm of drug discovery and targeted therapy. A vast evidence has demonstrated that antibody-based or alternatively aptamer-based strategy largely contributed to the elevated drug accumulation in tumors with reduced systematic cytotoxicity. This review describes the advanced progress of antisense oligonucleotides (ASOs), small interfering RNAs (siRNAs), microRNAs (miRNAs), messenger RNA (mRNAs), and aptamer-drug conjugates (ApDCs) in the treatment of PC, revealing the bright application and development direction in PC therapy.
引用
收藏
页数:17
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