2016
DOI: 10.1016/j.biomaterials.2015.09.037
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Nanomedicine-mediated cancer stem cell therapy

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Cited by 118 publications
(84 citation statements)
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“…37 Due to the EPR effect, nanocarriers have recently been used to deliver anti-CSC therapeutics to the tumor site to reduce the population of CSCs. 38,39 However, the drugs delivered by NPs often fail to transport to the CSCs due to the heterogeneity of the tumor and the high drug resistance of CSCs, which would Notes: The 2D-and 3D-cultured 4T1 breast cancer cells were treated with equivalent concentrations of (A) r6g-Peg-Plga, (B) r6g-ha-Peg-Plga, and (C) r6g-DclK1-ha-Peg-Plga NPs for 2 hours at 37°C. The immunofluorescence was visualized using a confocal microscope.…”
Section: Discussionmentioning
confidence: 99%
“…37 Due to the EPR effect, nanocarriers have recently been used to deliver anti-CSC therapeutics to the tumor site to reduce the population of CSCs. 38,39 However, the drugs delivered by NPs often fail to transport to the CSCs due to the heterogeneity of the tumor and the high drug resistance of CSCs, which would Notes: The 2D-and 3D-cultured 4T1 breast cancer cells were treated with equivalent concentrations of (A) r6g-Peg-Plga, (B) r6g-ha-Peg-Plga, and (C) r6g-DclK1-ha-Peg-Plga NPs for 2 hours at 37°C. The immunofluorescence was visualized using a confocal microscope.…”
Section: Discussionmentioning
confidence: 99%
“…These formulations use natural or synthetic polymeric materials to encapsulate or absorb drugs, and the carrier materials include polymers, liposomes, micelles, proteins, and metallic materials. Compared with traditional drug delivery systems, nanomedicine has the following advantages: it increases the bioavailability of poorly soluble drugs, prolongs drug circulation time, increases penetrability, permits loading of a variety of drugs, improves drug efficacy and targeting, and reduces toxicity [13,14]. These advantages have contributed to the research interest in nanomedicine-mediated combined chemotherapy and resulted in the successful development of some novel nanomedicine-anticancer drugs.…”
Section: Nanomedicinementioning
confidence: 99%
“…With this phenomenon in mind, an increasing number of CSCtargeted therapeutic agents have been developed over the past several years such as salinomycin, curcumin, thioridazine hydrochloride, sulforaphane, miR-34a, and miR-130b. [94][95][96][97] Despite their therapeutic potential in targeting CSCs, their clinical application has been hindered by their hydrophobicity, poor specificity and poor pharmacokinetics (PK) profiles. [98][99][100] Recent developments in nanoparticle delivery systems have provided new strategies to efficiently deliver therapeutics that can overcome the challenges posed by CSCs and improve therapeutic efficacy of CSC-targeting agents by controlling release kinetics, prolonging circulation time and improving bio-distribution.…”
Section: Nanomedicine In Combination Therapymentioning
confidence: 99%
“…Furthermore, in the study done by Wei and colleagues, salinomycin was conjugated to a hyaluronic acid-based nanogel to target CD44 + drug resistant cells which enhanced the therapeutic efficacy of salinomycin. [97,98] Another advantage of using nanoparticles is the additional capability to modify their surfaces with targeting agents such as mAbs and peptides. High target selectivity and internalization can be achieved by surface modification of nanoparticles with targeting moieties.…”
Section: Nanomedicine In Combination Therapymentioning
confidence: 99%
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