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human t24 bladder cancer cell line  (ATCC)


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    Structured Review

    ATCC human t24 bladder cancer cell line
    Human T24 Bladder Cancer Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 98/100, based on 2752 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+bladder+cancer+cell+lines/T24/pm42009646-537-0-9
    Average 98 stars, based on 2752 article reviews
    human t24 bladder cancer cell line - by Bioz Stars, 2026-09
    98/100 stars

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    Related Articles

    Derivative Assay:

    Article Title: CRISPR/Cas9-mediated miR-21 editing in high-grade urothelial carcinoma cells and its biological effects.
    Article Snippet: .. The human T24 cell line, derived from high-grade invasive urothelial carcinoma of the bladder, was obtained from the American Type Culture Collection (ATCC) and authenticated prior to use (Annex 1). ..

    other:

    Article Title: VEGF-C maturation mediated by CircFOCAD-orchestrated CCBE1 and ADAM10 expression in nuclear-cytoplasmic synergy drives lymphatic metastasis.
    Article Snippet: Cell line and cell culture In this study, the T24, UM-UC-3, and 5637 cell lines, which are human BCa cell lines, and SV-HUC-1, which is a normal human bladder epithelial cell line, were obtained from the American Type Culture Collection in Manassas, Virginia, USA and tested negative for mycoplasma contamination.

    Cell Culture:

    Article Title: Filamin C activates MAPK/ERK signaling to facilitate epithelial-mesenchymal transition in bladder cancer.
    Article Snippet: Background Bladder cancer (BC) is a prevalent malignancy with high metastatic and recurrent potential.. Filamin C (FLNC) has been reported implicated in various cancers, but its role in BC remains unclear.. Methods Bioinformatics analysis using The gene expression profiling interactive analysis (GEPIA) and The cancer genome atlas (TCGA) databases assessed FLNC expression, prognosis, and multivariate Cox regression in bladder urothelial carcinoma (BLCA).

    Article Title: Multiscale structural-rheological mapping of cancer spheroids during maturation.
    Article Snippet: .. We cultured spheroids from three cell lines: HCV29 – non-malignant transitional cell carcinoma of the ureter (established at the Institute of Experimental Therapy, PAN, Wroclaw, Poland),23 T24 – transitional cell carcinoma from ATCC (LGC Standards, Poland)24 and HT1376 – grade III urinary bladder cell carcinoma from ATCC (LGC Standards, Poland).25 Among the malignant cell lines, T24 is considered more aggressive than HT1376, reflecting its higher invasive potential.26 HCV29 and T24 were cultured in Roswell Park Memorial Institute Medium (RPMI) 1640 medium (Sigma-Aldrich, Poznań, Poland) supplemented with 10% of fetal bovine serum (FBS, Sigma-Aldrich, Poznań, Poland). .. HT1376 were grown in Eagle’s minimum essential medium (EMEM, LGC Standards, Poland) with 10% FBS.

    Article Title: Integrative multi-omics identifies a glycosylation-based prognostic framework and nominates ALG3 for targeted therapy in bladder cancer.
    Article Snippet: .. 2.8 Cell culture and functional assays Human bladder cancer cell lines UM-UC-3 and T24 (ATCC) were cultured in DMEM with 10% fetal bovine serum (Gibco) at 37 °C in 5% CO2. .. For ALG3 silencing, cells were transfected with 50 nM of two independent siRNAs AR TIC LE IN PR ES S targeting ALG3 or negative control (si-NC) using Lipofectamine® 3000 (Invitrogen).

    Functional Assay:

    Article Title: Integrative multi-omics identifies a glycosylation-based prognostic framework and nominates ALG3 for targeted therapy in bladder cancer.
    Article Snippet: .. 2.8 Cell culture and functional assays Human bladder cancer cell lines UM-UC-3 and T24 (ATCC) were cultured in DMEM with 10% fetal bovine serum (Gibco) at 37 °C in 5% CO2. .. For ALG3 silencing, cells were transfected with 50 nM of two independent siRNAs AR TIC LE IN PR ES S targeting ALG3 or negative control (si-NC) using Lipofectamine® 3000 (Invitrogen).



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    ATCC human bladder cancer cell lines t24
    Time-dependent cytotoxic effect of cisplatin and determination of IC 50 values in <t>T24</t> bladder cancer cells. Cell viability was evaluated at 24 and 48 h time points following exposure to increasing concentrations of cisplatin (0–40 µM). The resulting dose–response curves demonstrate that cisplatin decreases cell viability in a dose- and time-dependent manner. The horizontal dashed line represents 50% cell viability, while the vertical dashed lines indicate the corresponding IC 50 values at the respective time points. The lower IC 50 values observed at 48 h of exposure indicate the increasing cytotoxic effect of cisplatin over time.
    Human Bladder Cancer Cell Lines T24, supplied by ATCC, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC human t24 bladder cancer cell line
    Time-dependent cytotoxic effect of cisplatin and determination of IC 50 values in <t>T24</t> bladder cancer cells. Cell viability was evaluated at 24 and 48 h time points following exposure to increasing concentrations of cisplatin (0–40 µM). The resulting dose–response curves demonstrate that cisplatin decreases cell viability in a dose- and time-dependent manner. The horizontal dashed line represents 50% cell viability, while the vertical dashed lines indicate the corresponding IC 50 values at the respective time points. The lower IC 50 values observed at 48 h of exposure indicate the increasing cytotoxic effect of cisplatin over time.
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    ATCC human bladder cancer transitional epithelial tumor cell line
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    Image Search Results


    Time-dependent cytotoxic effect of cisplatin and determination of IC 50 values in T24 bladder cancer cells. Cell viability was evaluated at 24 and 48 h time points following exposure to increasing concentrations of cisplatin (0–40 µM). The resulting dose–response curves demonstrate that cisplatin decreases cell viability in a dose- and time-dependent manner. The horizontal dashed line represents 50% cell viability, while the vertical dashed lines indicate the corresponding IC 50 values at the respective time points. The lower IC 50 values observed at 48 h of exposure indicate the increasing cytotoxic effect of cisplatin over time.

    Journal: Biomedicines

    Article Title: Time-Dependent Effects of Cisplatin on Autophagy Gene Expression in Bladder Cancer Cells

    doi: 10.3390/biomedicines14051006

    Figure Lengend Snippet: Time-dependent cytotoxic effect of cisplatin and determination of IC 50 values in T24 bladder cancer cells. Cell viability was evaluated at 24 and 48 h time points following exposure to increasing concentrations of cisplatin (0–40 µM). The resulting dose–response curves demonstrate that cisplatin decreases cell viability in a dose- and time-dependent manner. The horizontal dashed line represents 50% cell viability, while the vertical dashed lines indicate the corresponding IC 50 values at the respective time points. The lower IC 50 values observed at 48 h of exposure indicate the increasing cytotoxic effect of cisplatin over time.

    Article Snippet: Human bladder cancer cell lines T24 and 5637 (ATCC, Manassas, VA, USA) were utilized in this study.

    Techniques:

    Time-dependent cytotoxic effect of cisplatin and determination of IC 50 values in 5637 bladder cancer cells. Cells were exposed to varying concentrations of cisplatin for 24 and 48 h, and cell viability was assessed. The dose–response curves indicate a more pronounced sensitivity to cisplatin in 5637 cells. The horizontal dashed line represents 50% cell viability, while the vertical dashed lines indicate the calculated IC 50 values. Lower IC 50 values compared to T24 cells demonstrate that this cell line is more sensitive.

    Journal: Biomedicines

    Article Title: Time-Dependent Effects of Cisplatin on Autophagy Gene Expression in Bladder Cancer Cells

    doi: 10.3390/biomedicines14051006

    Figure Lengend Snippet: Time-dependent cytotoxic effect of cisplatin and determination of IC 50 values in 5637 bladder cancer cells. Cells were exposed to varying concentrations of cisplatin for 24 and 48 h, and cell viability was assessed. The dose–response curves indicate a more pronounced sensitivity to cisplatin in 5637 cells. The horizontal dashed line represents 50% cell viability, while the vertical dashed lines indicate the calculated IC 50 values. Lower IC 50 values compared to T24 cells demonstrate that this cell line is more sensitive.

    Article Snippet: Human bladder cancer cell lines T24 and 5637 (ATCC, Manassas, VA, USA) were utilized in this study.

    Techniques:

    Time-dependent heatmap of autophagy-related gene expression in T24 and 5637 bladder cancer cells following cisplatin treatment. Relative expression levels (2 −ΔΔCt ) are shown for genes involved in autophagy initiation, elongation, selective autophagy, and lysosomal function across 0, 6, 24, and 48 h.

    Journal: Biomedicines

    Article Title: Time-Dependent Effects of Cisplatin on Autophagy Gene Expression in Bladder Cancer Cells

    doi: 10.3390/biomedicines14051006

    Figure Lengend Snippet: Time-dependent heatmap of autophagy-related gene expression in T24 and 5637 bladder cancer cells following cisplatin treatment. Relative expression levels (2 −ΔΔCt ) are shown for genes involved in autophagy initiation, elongation, selective autophagy, and lysosomal function across 0, 6, 24, and 48 h.

    Article Snippet: Human bladder cancer cell lines T24 and 5637 (ATCC, Manassas, VA, USA) were utilized in this study.

    Techniques: Gene Expression, Expressing

    Time-dependent expression profiles of autophagy-related genes in T24 and 5637 bladder cancer cell lines following cisplatin treatment. Relative mRNA expression levels of genes involved in autophagy initiation ( ULK1 , BECN1 ), elongation ( ATG5 , ATG7 , LC3B ), selective autophagy ( p62/SQSTM1 ), and lysosomal regulation (LAMP1 , TFEB ) were evaluated at 0, 6, 24, and 48 h post-treatment. Gene expression levels were calculated using the 2 −ΔΔCt method and are presented as fold changes relative to the control group (0 h). Blue bars represent the T24 cell line, and orange bars represent the 5637 cell line. Data are expressed as mean ± SEM of at least three independent experiments. * p < 0.05, ** p < 0.01 indicating statistical significance between the T24 and 5637 cell lines at the corresponding time points.

    Journal: Biomedicines

    Article Title: Time-Dependent Effects of Cisplatin on Autophagy Gene Expression in Bladder Cancer Cells

    doi: 10.3390/biomedicines14051006

    Figure Lengend Snippet: Time-dependent expression profiles of autophagy-related genes in T24 and 5637 bladder cancer cell lines following cisplatin treatment. Relative mRNA expression levels of genes involved in autophagy initiation ( ULK1 , BECN1 ), elongation ( ATG5 , ATG7 , LC3B ), selective autophagy ( p62/SQSTM1 ), and lysosomal regulation (LAMP1 , TFEB ) were evaluated at 0, 6, 24, and 48 h post-treatment. Gene expression levels were calculated using the 2 −ΔΔCt method and are presented as fold changes relative to the control group (0 h). Blue bars represent the T24 cell line, and orange bars represent the 5637 cell line. Data are expressed as mean ± SEM of at least three independent experiments. * p < 0.05, ** p < 0.01 indicating statistical significance between the T24 and 5637 cell lines at the corresponding time points.

    Article Snippet: Human bladder cancer cell lines T24 and 5637 (ATCC, Manassas, VA, USA) were utilized in this study.

    Techniques: Expressing, Gene Expression, Control