Recent Advances in siRNA Delivery Systems for Prostate Cancer Therapy

被引:9
作者
Aghamiri, Shahin [1 ,2 ]
Raee, Pourya [3 ]
Shahmohamadnejad, Shiva [4 ]
Shabani, Sasan [5 ]
Ghorbani, Jaber [6 ]
Sameni, Marzieh [7 ]
Ebrahimi, Mohammad Taha [7 ]
机构
[1] Shahid Beheshti Univ Med Sci, Sch Adv Technol Med, Dept Med Biotechnol, Tehran 193954818, Iran
[2] Shahid Beheshti Univ Med Sci, Cellular & Mol Biol Res Ctr, Tehran, Iran
[3] Shahid Beheshti Univ Med Sci, Sch Med, Dept Biol & Anat Sci, Tehran, Iran
[4] Univ Tehran Med Sci, Dept Biochem, Fac Med, Tehran, Iran
[5] Univ Tehran Med Sci, Sch Med, Dept Med Genet, Tehran, Iran
[6] Univ Tehran Med Sci, Sch Med, Dept Microbiol, Tehran, Iran
[7] Shahid Beheshti Univ Med Sci, Dept Med Biotechnol, Sch Adv Technol Med, Tehran, Iran
关键词
Prostate cancer; nanoparticles; siRNA; drug delivery systems; multidrug resistance; combination therapy; CELL-ADHESION MOLECULE; SMALL INTERFERING RNA; MULTIDRUG-RESISTANCE; CO-DELIVERY; DRUG-DELIVERY; ANTISENSE OLIGONUCLEOTIDE; TARGETED DELIVERY; CATIONIC NANOBUBBLES; ANTICANCER DRUGS; PHASE-I;
D O I
10.2174/1389201022666210615123211
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The critical problems of conventional prostate cancer therapeutic strategies like nonspecific toxicity and multi-drug resistance prompted the development and application of countless nanoparticle-based siRNA therapeutics. Unfortunately, siRNA-based therapeutics suffer from the lack of safe and effective delivery systems, immune system stimulation, poor knowledge of nano-bio interactions, and limitations concerning designing, manufacturing, clinical translation, and commercialization. In this review, we provide cutting-edge advances in nanoparticle-mediated siRNA delivery carriers like polymeric systems, lipid systems, specific systems, and rigid nanoparticles for the treatment of prostate cancer. Moreover, co-delivery of conventional chemotherapy drugs with siRNA as a revolutionary robust strategy for prostate cancer combinational therapy is completely covered.
引用
收藏
页码:579 / 593
页数:15
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