2020
DOI: 10.1007/s42242-020-00074-8
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A hepatocellular carcinoma–bone metastasis-on-a-chip model for studying thymoquinone-loaded anticancer nanoparticles

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Cited by 51 publications
(20 citation statements)
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“…Chitosan-coated PLGA NPs containing TQ enhanced cytotoxic potential when compared with surface-decorated TQ-poly(lactic co-glycolic acid) NPs and TQ alone; this was investigated through the MDA-MB-231 and MCF-7 cell lines [ 180 ]. The antimetastatic potential of TQ was enhanced by chitosan nanoparticles against HepG2 cell lines through longer duration inhibitory actions when compared with free TQ [ 181 ]. TQ-NLC-NPs accumulated in cancer cells and inhibited their proliferation through time and dose-dependent modulation in the cellular morphology, as investigated in HepG2 cancer cells [ 182 ].…”
Section: Neoplasm and Its Pathogenesismentioning
confidence: 99%
“…Chitosan-coated PLGA NPs containing TQ enhanced cytotoxic potential when compared with surface-decorated TQ-poly(lactic co-glycolic acid) NPs and TQ alone; this was investigated through the MDA-MB-231 and MCF-7 cell lines [ 180 ]. The antimetastatic potential of TQ was enhanced by chitosan nanoparticles against HepG2 cell lines through longer duration inhibitory actions when compared with free TQ [ 181 ]. TQ-NLC-NPs accumulated in cancer cells and inhibited their proliferation through time and dose-dependent modulation in the cellular morphology, as investigated in HepG2 cancer cells [ 182 ].…”
Section: Neoplasm and Its Pathogenesismentioning
confidence: 99%
“…Sharif et al developed an HCC-bone metastasis-on-achip system which models key aspects in the process of liver cancer invasion. This platform was used for studying the inhibitory effect of nanoparticle-encapsulated thymoquinone on the migration of HCC cells into the bone [111].…”
Section: Hcc-on-a-chipmentioning
confidence: 99%
“…Conversely, multiple-cell-type tumor-on-a-chip platforms (e.g., cancer, endothelial, stromal, and immune cells) have been used to investigate the specific crosstalk between different cell populations in the tumor microenvironments such as signaling cascades, tumor angiogenesis, and metastasis pathways ( Kolesky et al, 2014 ; Grolman et al, 2015 ; Sharifi et al, 2020 ; Cabon et al, 2021 ). Alternatively, 3D-bioprinted compartmented multiple-cell constructs have been used to create paracrine loops for studying cancer cell extravasation into the bloodstream and analyze metastatic progression through trans-endothelial migration ( Kolesky et al, 2014 ; Wang et al, 2018c ; Li J. et al, 2020 ).…”
Section: Tackling Current Biomedical Challenges With Frontier Technologiesmentioning
confidence: 99%