Recent advances in optimizing siRNA delivery to hepatocellular carcinoma cells

被引:0
作者
Weiskirchen, Ralf [1 ]
Weiskirchen, Sabine [1 ]
Grassi, Chiara [2 ]
Scaggiante, Bruna [3 ]
Grassi, Mario [4 ]
Tierno, Domenico [5 ]
Biasin, Alice [4 ,5 ]
Truong, Nhung Hai [6 ,7 ]
Minh, Thanh Dang [6 ,7 ]
Cemazar, Maja [8 ,9 ]
Pastorin, Giorgia [10 ]
Tonon, Federica [5 ]
Grassi, Gabriele [5 ]
机构
[1] RWTH Univ Hosp Aachen, Inst Mol Pathobiochem Expt Gene Therapy & Clin Che, Aachen, Germany
[2] Univ Trieste, Med, Trieste, Italy
[3] Trieste Univ, Dept Life Sci, Trieste, Italy
[4] Trieste Univ, Dept Engn & Architecture, Trieste, Italy
[5] Trieste Univ, Cattinara Univ Hosp, Clin Dept Med Surg & Hlth Sci, Str Fiume 447, I-34149 Trieste, Italy
[6] Univ Sci VNUHCM, Lab Regenerat Biomed, Ho Chi Minh City, Vietnam
[7] Viet Nam Natl Univ, Fac Biol & Biotechnol, Ho Chi Minh City, Vietnam
[8] Inst Oncol Ljubljana, Dept Expt Oncol, Ljubljana, Slovenia
[9] Univ Primorska, Fac Hlth Sci, Izola, Slovenia
[10] Natl Univ Singapore, Pharm Dept, Singapore, Singapore
关键词
Hepatocellular carcinoma; siRNAs; drug delivery materials; targeting; nano particle size; MONOCLONAL-ANTIBODIES; LIPID NANOPARTICLES; LIVER-CANCER; IN-VITRO; GENE; MECHANISM; RECEPTOR; RNAS; IDENTIFICATION; EXPRESSION;
D O I
10.1080/17425247.2025.2484287
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
IntroductionHepatocellularcarcinoma (HCC), the primary form of liver cancer, is the second leading cause of cancer-related deaths worldwide. Current therapies have limited effectiveness, particularly in advanced stages of the disease, highlighting the need for innovative treatment options. Small-interfering RNA(siRNA) molecules show great promise as a therapeutic solution since they can inhibit the expression of genes promoting HCC growth. Their cost-effective synthesis has further encouraged their potential use as novel drugs. However, siRNAs are vulnerable to degradation in biological environments, necessitating protective delivery systems. Additionally, targeted delivery to HCC is critical for optimal efficacy and minimal undesired side effects.AreacoveredThis review addresses the challenges associated with the delivery of siRNA toHCC, discussing and focusing on delivery systems based on lipid and polymeric nanoparticles in publications from the past five years.Expert opinionFuture nano particles will need to effectively cross the vessel wall, migrate through the extracellular matrix and finally cross the HCC cell membrane. This may be achieved by optimizing nanoparticle size, the equipment of nanoparticles withHCC targeting moieties and loading nanoparticles with siRNAs againstHCC-specific oncogenes.
引用
收藏
页码:729 / 745
页数:17
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