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human brain cancer stem cell bcsc line  (Celprogen Inc)


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    Structured Review

    Celprogen Inc human brain cancer stem cell bcsc line
    Human Brain Cancer Stem Cell Bcsc Line, supplied by Celprogen Inc, used in various techniques. Bioz Stars score: 94/100, based on 10 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+brain+cancer+stem+cells/Human+Brain+Cancer+Stem+Cells/pm41619048-67-1-10
    Average 94 stars, based on 10 article reviews
    human brain cancer stem cell bcsc line - by Bioz Stars, 2026-09
    94/100 stars

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    Related Articles

    Positron Emission Tomography:

    Article Title: Etoposide-loaded lipopolymer nanoparticles promote Smac minetic activity against inhibitor of apoptosis protein for glioblastoma treatment.
    Article Snippet: Encapsulated BV6 and SM164, two bivalent second mitochondria-derived activator of caspase (Smac) mimetics, in etoposide (ETO)-lipopolymer nanoparticles (NPs) have been developed to deplete inhibitor of apoptosis proteins (IAP), impair DNA, and produce antagonistic effects on glioblastoma multiforme (GBM) in nude mice.. The NPs, composed of cocoa butter (CB) and polyvinyl alcohol (PVA), were stabilized by glycerol monostearate and Pluronic F-127, and grafted with transferrin (Tf) and wheat germ agglutinin (WGA) to dock the blood-brain barrier (BBB) and degenerated dopaminergic neurons.. The dual-targeting NPs increased the BBB permeability of BV6, SM164 and ETO via recognizing Tf receptor (TfR) and N-acetylglucosamine that are abundantly expressed on brain microvascular endothelial cells.

    Membrane:

    Article Title: Etoposide-loaded lipopolymer nanoparticles promote Smac minetic activity against inhibitor of apoptosis protein for glioblastoma treatment.
    Article Snippet: Encapsulated BV6 and SM164, two bivalent second mitochondria-derived activator of caspase (Smac) mimetics, in etoposide (ETO)-lipopolymer nanoparticles (NPs) have been developed to deplete inhibitor of apoptosis proteins (IAP), impair DNA, and produce antagonistic effects on glioblastoma multiforme (GBM) in nude mice.. The NPs, composed of cocoa butter (CB) and polyvinyl alcohol (PVA), were stabilized by glycerol monostearate and Pluronic F-127, and grafted with transferrin (Tf) and wheat germ agglutinin (WGA) to dock the blood-brain barrier (BBB) and degenerated dopaminergic neurons.. The dual-targeting NPs increased the BBB permeability of BV6, SM164 and ETO via recognizing Tf receptor (TfR) and N-acetylglucosamine that are abundantly expressed on brain microvascular endothelial cells.

    CCK-8 Assay:

    Article Title: Etoposide-loaded lipopolymer nanoparticles promote Smac minetic activity against inhibitor of apoptosis protein for glioblastoma treatment.
    Article Snippet: Encapsulated BV6 and SM164, two bivalent second mitochondria-derived activator of caspase (Smac) mimetics, in etoposide (ETO)-lipopolymer nanoparticles (NPs) have been developed to deplete inhibitor of apoptosis proteins (IAP), impair DNA, and produce antagonistic effects on glioblastoma multiforme (GBM) in nude mice.. The NPs, composed of cocoa butter (CB) and polyvinyl alcohol (PVA), were stabilized by glycerol monostearate and Pluronic F-127, and grafted with transferrin (Tf) and wheat germ agglutinin (WGA) to dock the blood-brain barrier (BBB) and degenerated dopaminergic neurons.. The dual-targeting NPs increased the BBB permeability of BV6, SM164 and ETO via recognizing Tf receptor (TfR) and N-acetylglucosamine that are abundantly expressed on brain microvascular endothelial cells.

    Incubation:

    Article Title: Etoposide-loaded lipopolymer nanoparticles promote Smac minetic activity against inhibitor of apoptosis protein for glioblastoma treatment.
    Article Snippet: Encapsulated BV6 and SM164, two bivalent second mitochondria-derived activator of caspase (Smac) mimetics, in etoposide (ETO)-lipopolymer nanoparticles (NPs) have been developed to deplete inhibitor of apoptosis proteins (IAP), impair DNA, and produce antagonistic effects on glioblastoma multiforme (GBM) in nude mice.. The NPs, composed of cocoa butter (CB) and polyvinyl alcohol (PVA), were stabilized by glycerol monostearate and Pluronic F-127, and grafted with transferrin (Tf) and wheat germ agglutinin (WGA) to dock the blood-brain barrier (BBB) and degenerated dopaminergic neurons.. The dual-targeting NPs increased the BBB permeability of BV6, SM164 and ETO via recognizing Tf receptor (TfR) and N-acetylglucosamine that are abundantly expressed on brain microvascular endothelial cells.

    Enzyme-linked Immunosorbent Assay:

    Article Title: Etoposide-loaded lipopolymer nanoparticles promote Smac minetic activity against inhibitor of apoptosis protein for glioblastoma treatment.
    Article Snippet: Encapsulated BV6 and SM164, two bivalent second mitochondria-derived activator of caspase (Smac) mimetics, in etoposide (ETO)-lipopolymer nanoparticles (NPs) have been developed to deplete inhibitor of apoptosis proteins (IAP), impair DNA, and produce antagonistic effects on glioblastoma multiforme (GBM) in nude mice.. The NPs, composed of cocoa butter (CB) and polyvinyl alcohol (PVA), were stabilized by glycerol monostearate and Pluronic F-127, and grafted with transferrin (Tf) and wheat germ agglutinin (WGA) to dock the blood-brain barrier (BBB) and degenerated dopaminergic neurons.. The dual-targeting NPs increased the BBB permeability of BV6, SM164 and ETO via recognizing Tf receptor (TfR) and N-acetylglucosamine that are abundantly expressed on brain microvascular endothelial cells.



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    Expression levels of miR- 155 - 5p. a ) Expression levels in glioblastoma and healthy brain tissues (To compare gene expression levels across different samples regardless of sequencing depth, Reads Per Million (RPM) is calculated by dividing the raw read count of a given transcript by the total number of mapped reads in the sample and multiplying by 10 6 .); b ) Expression levels in <t>BCSCs</t> compared <t>to</t> <t>BSCs</t> (RPM: Reads per million); c) Expression levels in anti-miR- 155 - 5p treated BCSCs and BSCs compared to untreated control cells Statistical significance was evaluated by Student’s t-test ( p < 0.05: *, p < 0.01: **, p < 0.001: ***, p < 0.0001: ****)
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    Expression levels of miR- 155 - 5p. a ) Expression levels in glioblastoma and healthy brain tissues (To compare gene expression levels across different samples regardless of sequencing depth, Reads Per Million (RPM) is calculated by dividing the raw read count of a given transcript by the total number of mapped reads in the sample and multiplying by 10 6 .); b ) Expression levels in <t>BCSCs</t> compared <t>to</t> <t>BSCs</t> (RPM: Reads per million); c) Expression levels in anti-miR- 155 - 5p treated BCSCs and BSCs compared to untreated control cells Statistical significance was evaluated by Student’s t-test ( p < 0.05: *, p < 0.01: **, p < 0.001: ***, p < 0.0001: ****)
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    Expression levels of miR- 155 - 5p. a ) Expression levels in glioblastoma and healthy brain tissues (To compare gene expression levels across different samples regardless of sequencing depth, Reads Per Million (RPM) is calculated by dividing the raw read count of a given transcript by the total number of mapped reads in the sample and multiplying by 10 6 .); b ) Expression levels in BCSCs compared to BSCs (RPM: Reads per million); c) Expression levels in anti-miR- 155 - 5p treated BCSCs and BSCs compared to untreated control cells Statistical significance was evaluated by Student’s t-test ( p < 0.05: *, p < 0.01: **, p < 0.001: ***, p < 0.0001: ****)

    Journal: Naunyn-Schmiedeberg's Archives of Pharmacology

    Article Title: Anti-miRNA- 155 - 5p enhances the cytotoxic efficacy of temozolomide in brain cancer stem cells

    doi: 10.1007/s00210-025-04135-6

    Figure Lengend Snippet: Expression levels of miR- 155 - 5p. a ) Expression levels in glioblastoma and healthy brain tissues (To compare gene expression levels across different samples regardless of sequencing depth, Reads Per Million (RPM) is calculated by dividing the raw read count of a given transcript by the total number of mapped reads in the sample and multiplying by 10 6 .); b ) Expression levels in BCSCs compared to BSCs (RPM: Reads per million); c) Expression levels in anti-miR- 155 - 5p treated BCSCs and BSCs compared to untreated control cells Statistical significance was evaluated by Student’s t-test ( p < 0.05: *, p < 0.01: **, p < 0.001: ***, p < 0.0001: ****)

    Article Snippet: BCSCs were obtained from Celprogen (Catalog No: 36110–37), and BSCs were sourced from the same provider (Catalog No: 36109–36, USA).

    Techniques: Expressing, Gene Expression, Sequencing, Control