2021
DOI: 10.1016/j.jmst.2020.03.009
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Targeted combination therapy for glioblastoma by co-delivery of doxorubicin, YAP-siRNA and gold nanorods

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Cited by 11 publications
(5 citation statements)
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“…D/R@Ang2-Lip+Au, a doxorubicin-and YAP-siRNA-loaded cationic liposome, was able to effectively inhibit glioblastoma. 369 In addition, another YAP-siRNAlipid nanoparticle repressed hepatocellular carcinoma in a mouse model. 370 In addition to cancer treatment, YAP-siRNA was effective in treating posterior segment neovascularization-related ocular diseases.…”
Section: Dysregulation Of the Hippo Pathway And Human Diseasesmentioning
confidence: 99%
“…D/R@Ang2-Lip+Au, a doxorubicin-and YAP-siRNA-loaded cationic liposome, was able to effectively inhibit glioblastoma. 369 In addition, another YAP-siRNAlipid nanoparticle repressed hepatocellular carcinoma in a mouse model. 370 In addition to cancer treatment, YAP-siRNA was effective in treating posterior segment neovascularization-related ocular diseases.…”
Section: Dysregulation Of the Hippo Pathway And Human Diseasesmentioning
confidence: 99%
“…In addition, the system inhibited tumorigenesis, induced CD133+ glioma cell apoptosis, and prolonged survival in intracranial glioma tumor-bearing nude mice. Recently, synergistic tumor-inhibitory effects were also noted with an Angiopep-2 decorated cationic liposome that simultaneously delivered doxorubicin, yes-associated protein (YAP) siRNA, and gold nanorods [129].…”
Section: Drug and Nucleic Acid Co-deliverymentioning
confidence: 99%
“…For example, DNA and RNA strands are stabilized on the surface of GNRs in different nanosystem designs for brain drug delivery. GNRs have been applied in a nanosystem designed for glioblastoma therapy by combining thermal therapy and inhibiting a protein expression, which is expected to make the glioblastoma more sensitive to chemotherapy [ 131 ]. The system consists of a liposome with a cationic-charged surface, modified by angiopep-2 peptide and loaded internally with DOX (a chemotherapeutic agent) and externally with GNRs (photothermal therapeutic agents) and yes-associated protein siRNA (YAP-siRNA), responsible for inhibiting the expression of YAP protein ( Figure 2 A).…”
Section: Gnrs For Therapeutic Applicationsmentioning
confidence: 99%
“…The system consists of a liposome with a cationic-charged surface, modified by angiopep-2 peptide and loaded internally with DOX (a chemotherapeutic agent) and externally with GNRs (photothermal therapeutic agents) and yes-associated protein siRNA (YAP-siRNA), responsible for inhibiting the expression of YAP protein ( Figure 2 A). The system showed good tumor growth inhibition effects and could pass the blood–brain barrier [ 131 ].…”
Section: Gnrs For Therapeutic Applicationsmentioning
confidence: 99%
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