A new antisense oligonucleotide delivery system based on self-assembled ODN–PEG hybrid conjugate micelles

2003 ◽  
Vol 93 (2) ◽  
pp. 183-191 ◽  
Author(s):  
J Jeong
2014 ◽  
Vol 15 (9) ◽  
pp. 847-855 ◽  
Author(s):  
Raquel Petrilli ◽  
Josimar Eloy ◽  
Juliana Marchetti ◽  
Renata Lopez ◽  
Robert Lee

2020 ◽  
Vol 229 ◽  
pp. 115451 ◽  
Author(s):  
S. Leitner ◽  
S. Grijalvo ◽  
C. Solans ◽  
R. Eritja ◽  
M.J. García-Celma ◽  
...  

2020 ◽  
Vol 3 (11) ◽  
pp. 7831-7839
Author(s):  
Xiao-He Ren ◽  
Xiao-Yan He ◽  
Bo-Ya Liu ◽  
Chang Xu ◽  
Si-Xue Cheng

2021 ◽  
Author(s):  
husun qian ◽  
Yixin Fu ◽  
Minkang Guo ◽  
Wu Yang ◽  
Dian Zhang ◽  
...  

Abstract There is increasing interest in depleting or repolarizing tumor-associated macrophages (TAMs) to generate a pro-inflammatory effect. However, TAMs usually display an immunosuppressive M2-like phenotype in tumor microenvironment. Apparently, developing a macrophage targeting delivery system with immunomodulatory agents is urgent. In the study, an efficient siRNAs and CpG ODNs delivery system (CpG-siRNA-tFNA) was prepared with nucleic acid stepwise self-assembled. The tFNA composed of CpG ODNs and siRNAs showed a higher stability and an enhanced cellular uptake efficiency. Moreover, the CpG-siRNA-tFNA effectively reprogrammed TAMs toward M1 phenotype polarization with increased pro-inflammatory cytokines secretion and NF-κB signal pathways activation, which triggers dramatical antitumor immune responses. Hence, we have developed an efficient and reliable TAM-targeted therapeutic with immunomodulatory agents for for clinical applications.


2019 ◽  
Vol 2 (11) ◽  
pp. 4737-4746
Author(s):  
Tengfei Wang ◽  
Shanni Hong ◽  
Yu Luo ◽  
Haiyin Lv ◽  
Ye Zhang ◽  
...  

2020 ◽  
Vol 8 (16) ◽  
pp. 3527-3533 ◽  
Author(s):  
Lairong Ding ◽  
Junwei Li ◽  
Changrong Wu ◽  
Feng Yan ◽  
Xuemei Li ◽  
...  

A novel RNA-triple-helix hydrogel for treatment of triple negative breast cancers (TNBCs) by incorporating RNA-triple-helix and siRNA duplexes of CXCR4 into the same RNA nanoparticles was developed, without the synthetic polycationic reagents.


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