2023
DOI: 10.1016/j.ijbiomac.2022.11.242
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Enhancing the antitumor immunosurveillance of PD-L1-targeted gene therapy for metastatic melanoma using cationized Panax Notoginseng polysaccharide

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Cited by 11 publications
(7 citation statements)
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“…18 Polysaccharides can resist tumor development by activating macrophages and lymphocytes, promoting cytokine secretion, and improving host antitumor immune function. [19][20][21] Macrophages are the primary immunoregulatory cells in tumors and play a vital role in the tumor immune response. 22 The polarization of TAMs is ubiquitous in tumorigenesis and development.…”
Section: Conclusion and Discussionmentioning
confidence: 99%
“…18 Polysaccharides can resist tumor development by activating macrophages and lymphocytes, promoting cytokine secretion, and improving host antitumor immune function. [19][20][21] Macrophages are the primary immunoregulatory cells in tumors and play a vital role in the tumor immune response. 22 The polarization of TAMs is ubiquitous in tumorigenesis and development.…”
Section: Conclusion and Discussionmentioning
confidence: 99%
“…The designed PNP-PEI loaded with short hairpin RNA targeting the PD-L1 exhibited immunopotentiating therapeutic results in tumor immunotherapy. 466 Furthermore, advances in the utilization of poly(ethylene glycol)-grafted-polyethylenimine (PEI-g-PEG) as a delivery vehicle for mRNA therapeutics have been noteworthy. Specifically, different terminal functional groups and grafting ratios of PEG were explored for their influence on transgene expression levels.…”
Section: Diverse Polymer Selection Based On Therapeuticmentioning
confidence: 99%
“…Positively charged PEI has also been grafted onto the backbone of Panax notoginseng polysaccharide (PNP) to enable charge reversal and produce a functional RNA vector (PNP-PEI). The designed PNP-PEI loaded with short hairpin RNA targeting the PD-L1 exhibited immunopotentiating therapeutic results in tumor immunotherapy . Furthermore, advances in the utilization of poly­(ethylene glycol)-grafted-polyethylenimine (PEI-g-PEG) as a delivery vehicle for mRNA therapeutics have been noteworthy.…”
Section: Chemical Modifications On Rna Nanodelivery Platformsmentioning
confidence: 99%
“…Astragalus membranaceus root extract Polysaccharide nanoparticles [8,9] Cellobiose Cryoprotectant for liposomes [10] Chia seed oil from Salvia hispanica L. Liposomes and nanoemulsions [11] Chitosan extracted from fungi (Aspergillus niger; Agaricus bisporus) Chitosan nanoparticles [8,12,13] Chondroitin sulphate (synthetic) Polysaccharide nanoparticles [14][15][16] Coagulated potato proteins Protein-based nanoparticles [17,18] Dextran from Leuconostoc mesenteroides Polysaccharide nanoparticles Reviewed by [19] Digitaria exilis Polysaccharide nanoparticles [20] Eggshell membrane protein hydrolysate Protein-based nanoparticles [21][22][23] Fucoidan extracted from the seaweed Fucus vesiculosus and Undaria pinnatifida Polysaccharide nanoparticles [24][25][26] Guar gum Polysaccharide nanoparticles [27] Lucerne leaf extract from Medicago sativa Protein-based nanoparticles [28] Mung bean seed proteins from Vigna radiata Protein-based nanoparticles [29,30] Panax notoginseng root extract Polysaccharide nanoparticles [31] Phytoglycogen Polysaccharide nanoparticles Polyelectrolyte complex [32][33][34][35][36][37] Phytosterols Solid lipid nanoparticles Liposomes [38,39] Phospholipids from egg yolk Liposomes [40][41][42] Phosphatidylserine from soya and fish phospholipids Liposomes [43,44] Rapeseed protein from Brassica nap...…”
Section: Material(s) From Novel Foods Type Of Carrier Referencesmentioning
confidence: 99%