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a498 human renal adenocarcinomas  (ATCC)


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    Structured Review

    ATCC a498 human renal adenocarcinomas
    ( A ) Schematic illustration of the experimental setup with four groups: (i) unmodified 293T cells, (ii) 293T cells modified with GFP only, (iii) 293T cells modified with TRAIL + GFP , and (iv) cell-based microrobots—293T cells modified with TRAIL + GFP and then conjugated to magnetic Janus particles. 293T cells were seeded in the upper chamber of a transwell system; healthy hAMSCs or <t>A498</t> cancer cells were seeded in the lower chamber. Cell viability was assessed after 3 days of coculture. Created in BioRender. N. O. Dogan (2026), https://biorender.com/3lke7fg . ( B ) TRAIL secretion was measured in all groups at 48 hours posttransfection. Data are presented as the means ± SD from n = 3 technical replicates. One-way ANOVA with Tukey’s post hoc test; n.s. indicates P ≥ 0.05, and **** P < 0.0001. ( C ) CellTiter-Glo viability assays showing a minimal effect on healthy hAMSC viability across groups, while A498 cancer cells exhibited significant death in both TRAIL + GFP and TRAIL + GFP + particles groups. Data are presented as the means ± SD from n = 10 technical replicates. One-way ANOVA with Tukey’s post hoc test; n.s. indicates P ≥ 0.05; * P < 0.05, ** P < 0.01, and **** P < 0.0001. ( D ) Representative live/dead fluorescence images confirming the selective cytotoxicity of cell-based microrobots on A498 cancer cells, with no detectable harm on healthy hAMSCs. Scale bars, 100 μm.
    A498 Human Renal Adenocarcinomas, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 1673 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/a498+human+renal+adenocarcinomas/A-498/pmc13127565-275-2-6
    Average 97 stars, based on 1673 article reviews
    a498 human renal adenocarcinomas - by Bioz Stars, 2026-10
    97/100 stars

    Images

    1) Product Images from "Genetically engineered human cell–based microrobots for selective cancer cell death"

    Article Title: Genetically engineered human cell–based microrobots for selective cancer cell death

    Journal: Science Advances

    doi: 10.1126/sciadv.aea9831

    ( A ) Schematic illustration of the experimental setup with four groups: (i) unmodified 293T cells, (ii) 293T cells modified with GFP only, (iii) 293T cells modified with TRAIL + GFP , and (iv) cell-based microrobots—293T cells modified with TRAIL + GFP and then conjugated to magnetic Janus particles. 293T cells were seeded in the upper chamber of a transwell system; healthy hAMSCs or A498 cancer cells were seeded in the lower chamber. Cell viability was assessed after 3 days of coculture. Created in BioRender. N. O. Dogan (2026), https://biorender.com/3lke7fg . ( B ) TRAIL secretion was measured in all groups at 48 hours posttransfection. Data are presented as the means ± SD from n = 3 technical replicates. One-way ANOVA with Tukey’s post hoc test; n.s. indicates P ≥ 0.05, and **** P < 0.0001. ( C ) CellTiter-Glo viability assays showing a minimal effect on healthy hAMSC viability across groups, while A498 cancer cells exhibited significant death in both TRAIL + GFP and TRAIL + GFP + particles groups. Data are presented as the means ± SD from n = 10 technical replicates. One-way ANOVA with Tukey’s post hoc test; n.s. indicates P ≥ 0.05; * P < 0.05, ** P < 0.01, and **** P < 0.0001. ( D ) Representative live/dead fluorescence images confirming the selective cytotoxicity of cell-based microrobots on A498 cancer cells, with no detectable harm on healthy hAMSCs. Scale bars, 100 μm.
    Figure Legend Snippet: ( A ) Schematic illustration of the experimental setup with four groups: (i) unmodified 293T cells, (ii) 293T cells modified with GFP only, (iii) 293T cells modified with TRAIL + GFP , and (iv) cell-based microrobots—293T cells modified with TRAIL + GFP and then conjugated to magnetic Janus particles. 293T cells were seeded in the upper chamber of a transwell system; healthy hAMSCs or A498 cancer cells were seeded in the lower chamber. Cell viability was assessed after 3 days of coculture. Created in BioRender. N. O. Dogan (2026), https://biorender.com/3lke7fg . ( B ) TRAIL secretion was measured in all groups at 48 hours posttransfection. Data are presented as the means ± SD from n = 3 technical replicates. One-way ANOVA with Tukey’s post hoc test; n.s. indicates P ≥ 0.05, and **** P < 0.0001. ( C ) CellTiter-Glo viability assays showing a minimal effect on healthy hAMSC viability across groups, while A498 cancer cells exhibited significant death in both TRAIL + GFP and TRAIL + GFP + particles groups. Data are presented as the means ± SD from n = 10 technical replicates. One-way ANOVA with Tukey’s post hoc test; n.s. indicates P ≥ 0.05; * P < 0.05, ** P < 0.01, and **** P < 0.0001. ( D ) Representative live/dead fluorescence images confirming the selective cytotoxicity of cell-based microrobots on A498 cancer cells, with no detectable harm on healthy hAMSCs. Scale bars, 100 μm.

    Techniques Used: Modification, Fluorescence

    ( A ) Differential interference contrast imaging demonstrating the magnetic guidance of cell-based microrobots toward a 3D tumor spheroid. Scale bars, 100 μm. ( B ) As shown by live/dead fluorescence imaging, conditioned medium from cell-based microrobots induced increased tumor cell death in 3D A498 renal adenocarcinoma tumor spheroids, unlike medium from unmodified 293T cells. Scale bars, 100 μm. ( C ) CellTiter-Glo 3D assay revealed significantly reduced tumor spheroid viability after 24 hours of incubation with conditioned medium from cell-based microrobots compared to medium from unmodified 293T cells. Data are presented as the means ± SD, n = 6 technical replicates. One-way ANOVA with Tukey’s post hoc test; **** P < 0.0001.
    Figure Legend Snippet: ( A ) Differential interference contrast imaging demonstrating the magnetic guidance of cell-based microrobots toward a 3D tumor spheroid. Scale bars, 100 μm. ( B ) As shown by live/dead fluorescence imaging, conditioned medium from cell-based microrobots induced increased tumor cell death in 3D A498 renal adenocarcinoma tumor spheroids, unlike medium from unmodified 293T cells. Scale bars, 100 μm. ( C ) CellTiter-Glo 3D assay revealed significantly reduced tumor spheroid viability after 24 hours of incubation with conditioned medium from cell-based microrobots compared to medium from unmodified 293T cells. Data are presented as the means ± SD, n = 6 technical replicates. One-way ANOVA with Tukey’s post hoc test; **** P < 0.0001.

    Techniques Used: Imaging, Fluorescence, Incubation

    Related Articles

    Modification:

    Article Title: Genetically engineered human cell–based microrobots for selective cancer cell death
    Article Snippet: 293T human embryonic kidney cells (DSMZ), BJ human fibroblasts [American Type Culture Collection (ATCC)], hAMSCs (Cellular Engineering Technologies), HCT116 human colorectal carcinoma cells (ATCC), and T98G human glioblastoma cells (ATCC) were maintained in high-glucose Dulbecco’s modified Eagle’s medium (Gibco).293T human embryonic kidney cells (DSMZ), BJ human fibroblasts [American Type Culture Collection (ATCC)], hAMSCs (Cellular Engineering Technologies), HCT116 human colorectal carcinoma cells (ATCC), and T98G human glioblastoma cells (ATCC) were maintained in high-glucose Dulbecco’s modified Eagle’s medium (Gibco).. ACHN and A498 human renal adenocarcinomas (ATCC) and ONCO-DG-1 human ovarian adenocarcinomas (DSMZ) were cultivated in Roswell Park Memorial Institute (RPMI) 1640 medium (Gibco).. All culture media were supplemented with 10% fetal bovine serum (Gibco) and 1% penicillin-streptomycin (Gibco).All culture media were supplemented with 10% fetal bovine serum (Gibco) and 1% penicillin-streptomycin (Gibco).

    Fluorescence:

    Article Title: Genetically engineered human cell–based microrobots for selective cancer cell death
    Article Snippet: 293T human embryonic kidney cells (DSMZ), BJ human fibroblasts [American Type Culture Collection (ATCC)], hAMSCs (Cellular Engineering Technologies), HCT116 human colorectal carcinoma cells (ATCC), and T98G human glioblastoma cells (ATCC) were maintained in high-glucose Dulbecco’s modified Eagle’s medium (Gibco).293T human embryonic kidney cells (DSMZ), BJ human fibroblasts [American Type Culture Collection (ATCC)], hAMSCs (Cellular Engineering Technologies), HCT116 human colorectal carcinoma cells (ATCC), and T98G human glioblastoma cells (ATCC) were maintained in high-glucose Dulbecco’s modified Eagle’s medium (Gibco).. ACHN and A498 human renal adenocarcinomas (ATCC) and ONCO-DG-1 human ovarian adenocarcinomas (DSMZ) were cultivated in Roswell Park Memorial Institute (RPMI) 1640 medium (Gibco).. All culture media were supplemented with 10% fetal bovine serum (Gibco) and 1% penicillin-streptomycin (Gibco).All culture media were supplemented with 10% fetal bovine serum (Gibco) and 1% penicillin-streptomycin (Gibco).

    Imaging:

    Article Title: Genetically engineered human cell–based microrobots for selective cancer cell death
    Article Snippet: 293T human embryonic kidney cells (DSMZ), BJ human fibroblasts [American Type Culture Collection (ATCC)], hAMSCs (Cellular Engineering Technologies), HCT116 human colorectal carcinoma cells (ATCC), and T98G human glioblastoma cells (ATCC) were maintained in high-glucose Dulbecco’s modified Eagle’s medium (Gibco).293T human embryonic kidney cells (DSMZ), BJ human fibroblasts [American Type Culture Collection (ATCC)], hAMSCs (Cellular Engineering Technologies), HCT116 human colorectal carcinoma cells (ATCC), and T98G human glioblastoma cells (ATCC) were maintained in high-glucose Dulbecco’s modified Eagle’s medium (Gibco).. ACHN and A498 human renal adenocarcinomas (ATCC) and ONCO-DG-1 human ovarian adenocarcinomas (DSMZ) were cultivated in Roswell Park Memorial Institute (RPMI) 1640 medium (Gibco).. All culture media were supplemented with 10% fetal bovine serum (Gibco) and 1% penicillin-streptomycin (Gibco).All culture media were supplemented with 10% fetal bovine serum (Gibco) and 1% penicillin-streptomycin (Gibco).

    Incubation:

    Article Title: Genetically engineered human cell–based microrobots for selective cancer cell death
    Article Snippet: 293T human embryonic kidney cells (DSMZ), BJ human fibroblasts [American Type Culture Collection (ATCC)], hAMSCs (Cellular Engineering Technologies), HCT116 human colorectal carcinoma cells (ATCC), and T98G human glioblastoma cells (ATCC) were maintained in high-glucose Dulbecco’s modified Eagle’s medium (Gibco).293T human embryonic kidney cells (DSMZ), BJ human fibroblasts [American Type Culture Collection (ATCC)], hAMSCs (Cellular Engineering Technologies), HCT116 human colorectal carcinoma cells (ATCC), and T98G human glioblastoma cells (ATCC) were maintained in high-glucose Dulbecco’s modified Eagle’s medium (Gibco).. ACHN and A498 human renal adenocarcinomas (ATCC) and ONCO-DG-1 human ovarian adenocarcinomas (DSMZ) were cultivated in Roswell Park Memorial Institute (RPMI) 1640 medium (Gibco).. All culture media were supplemented with 10% fetal bovine serum (Gibco) and 1% penicillin-streptomycin (Gibco).All culture media were supplemented with 10% fetal bovine serum (Gibco) and 1% penicillin-streptomycin (Gibco).



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    97
    ATCC a498 human renal adenocarcinomas
    ( A ) Schematic illustration of the experimental setup with four groups: (i) unmodified 293T cells, (ii) 293T cells modified with GFP only, (iii) 293T cells modified with TRAIL + GFP , and (iv) cell-based microrobots—293T cells modified with TRAIL + GFP and then conjugated to magnetic Janus particles. 293T cells were seeded in the upper chamber of a transwell system; healthy hAMSCs or <t>A498</t> cancer cells were seeded in the lower chamber. Cell viability was assessed after 3 days of coculture. Created in BioRender. N. O. Dogan (2026), https://biorender.com/3lke7fg . ( B ) TRAIL secretion was measured in all groups at 48 hours posttransfection. Data are presented as the means ± SD from n = 3 technical replicates. One-way ANOVA with Tukey’s post hoc test; n.s. indicates P ≥ 0.05, and **** P < 0.0001. ( C ) CellTiter-Glo viability assays showing a minimal effect on healthy hAMSC viability across groups, while A498 cancer cells exhibited significant death in both TRAIL + GFP and TRAIL + GFP + particles groups. Data are presented as the means ± SD from n = 10 technical replicates. One-way ANOVA with Tukey’s post hoc test; n.s. indicates P ≥ 0.05; * P < 0.05, ** P < 0.01, and **** P < 0.0001. ( D ) Representative live/dead fluorescence images confirming the selective cytotoxicity of cell-based microrobots on A498 cancer cells, with no detectable harm on healthy hAMSCs. Scale bars, 100 μm.
    A498 Human Renal Adenocarcinomas, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/a498+human+renal+adenocarcinomas/A-498/pmc13127565-275-2-6
    Average 97 stars, based on 1 article reviews
    a498 human renal adenocarcinomas - by Bioz Stars, 2026-10
    97/100 stars
      Buy from Supplier

    97
    ATCC human renal adenocarcinoma cell lines a498
    Fig. 2 HHLA2 expression is induced on <t>A498</t> ccRCC cell line in vivo. A Expression of HHLA2 on A498 cells in vitro. B-G Five million A498 or 786-O cells were injected subcutaneously into NSG mice and tumors were harvested at a size of at least 10 mm. HHLA2 expression was analyzed by (B) flow cytometry on day 0 and after 1, 4, and 7 days of culture in vitro (numbers in upper right indicate % HHLA2 positive) and (C) by immunohistochemistry on day 0. D-G representative H&E and HHLA2 images of A498 and 786-O tumors, respectively. The statistical significance of difference versus control cells is indicated as ****p < 0.0001
    Human Renal Adenocarcinoma Cell Lines A498, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/a498+human+renal+adenocarcinomas/A-498/pm37891555-53-0-25
    Average 97 stars, based on 1 article reviews
    human renal adenocarcinoma cell lines a498 - by Bioz Stars, 2026-10
    97/100 stars
      Buy from Supplier

    Image Search Results


    ( A ) Schematic illustration of the experimental setup with four groups: (i) unmodified 293T cells, (ii) 293T cells modified with GFP only, (iii) 293T cells modified with TRAIL + GFP , and (iv) cell-based microrobots—293T cells modified with TRAIL + GFP and then conjugated to magnetic Janus particles. 293T cells were seeded in the upper chamber of a transwell system; healthy hAMSCs or A498 cancer cells were seeded in the lower chamber. Cell viability was assessed after 3 days of coculture. Created in BioRender. N. O. Dogan (2026), https://biorender.com/3lke7fg . ( B ) TRAIL secretion was measured in all groups at 48 hours posttransfection. Data are presented as the means ± SD from n = 3 technical replicates. One-way ANOVA with Tukey’s post hoc test; n.s. indicates P ≥ 0.05, and **** P < 0.0001. ( C ) CellTiter-Glo viability assays showing a minimal effect on healthy hAMSC viability across groups, while A498 cancer cells exhibited significant death in both TRAIL + GFP and TRAIL + GFP + particles groups. Data are presented as the means ± SD from n = 10 technical replicates. One-way ANOVA with Tukey’s post hoc test; n.s. indicates P ≥ 0.05; * P < 0.05, ** P < 0.01, and **** P < 0.0001. ( D ) Representative live/dead fluorescence images confirming the selective cytotoxicity of cell-based microrobots on A498 cancer cells, with no detectable harm on healthy hAMSCs. Scale bars, 100 μm.

    Journal: Science Advances

    Article Title: Genetically engineered human cell–based microrobots for selective cancer cell death

    doi: 10.1126/sciadv.aea9831

    Figure Lengend Snippet: ( A ) Schematic illustration of the experimental setup with four groups: (i) unmodified 293T cells, (ii) 293T cells modified with GFP only, (iii) 293T cells modified with TRAIL + GFP , and (iv) cell-based microrobots—293T cells modified with TRAIL + GFP and then conjugated to magnetic Janus particles. 293T cells were seeded in the upper chamber of a transwell system; healthy hAMSCs or A498 cancer cells were seeded in the lower chamber. Cell viability was assessed after 3 days of coculture. Created in BioRender. N. O. Dogan (2026), https://biorender.com/3lke7fg . ( B ) TRAIL secretion was measured in all groups at 48 hours posttransfection. Data are presented as the means ± SD from n = 3 technical replicates. One-way ANOVA with Tukey’s post hoc test; n.s. indicates P ≥ 0.05, and **** P < 0.0001. ( C ) CellTiter-Glo viability assays showing a minimal effect on healthy hAMSC viability across groups, while A498 cancer cells exhibited significant death in both TRAIL + GFP and TRAIL + GFP + particles groups. Data are presented as the means ± SD from n = 10 technical replicates. One-way ANOVA with Tukey’s post hoc test; n.s. indicates P ≥ 0.05; * P < 0.05, ** P < 0.01, and **** P < 0.0001. ( D ) Representative live/dead fluorescence images confirming the selective cytotoxicity of cell-based microrobots on A498 cancer cells, with no detectable harm on healthy hAMSCs. Scale bars, 100 μm.

    Article Snippet: ACHN and A498 human renal adenocarcinomas (ATCC) and ONCO-DG-1 human ovarian adenocarcinomas (DSMZ) were cultivated in Roswell Park Memorial Institute (RPMI) 1640 medium (Gibco).

    Techniques: Modification, Fluorescence

    ( A ) Differential interference contrast imaging demonstrating the magnetic guidance of cell-based microrobots toward a 3D tumor spheroid. Scale bars, 100 μm. ( B ) As shown by live/dead fluorescence imaging, conditioned medium from cell-based microrobots induced increased tumor cell death in 3D A498 renal adenocarcinoma tumor spheroids, unlike medium from unmodified 293T cells. Scale bars, 100 μm. ( C ) CellTiter-Glo 3D assay revealed significantly reduced tumor spheroid viability after 24 hours of incubation with conditioned medium from cell-based microrobots compared to medium from unmodified 293T cells. Data are presented as the means ± SD, n = 6 technical replicates. One-way ANOVA with Tukey’s post hoc test; **** P < 0.0001.

    Journal: Science Advances

    Article Title: Genetically engineered human cell–based microrobots for selective cancer cell death

    doi: 10.1126/sciadv.aea9831

    Figure Lengend Snippet: ( A ) Differential interference contrast imaging demonstrating the magnetic guidance of cell-based microrobots toward a 3D tumor spheroid. Scale bars, 100 μm. ( B ) As shown by live/dead fluorescence imaging, conditioned medium from cell-based microrobots induced increased tumor cell death in 3D A498 renal adenocarcinoma tumor spheroids, unlike medium from unmodified 293T cells. Scale bars, 100 μm. ( C ) CellTiter-Glo 3D assay revealed significantly reduced tumor spheroid viability after 24 hours of incubation with conditioned medium from cell-based microrobots compared to medium from unmodified 293T cells. Data are presented as the means ± SD, n = 6 technical replicates. One-way ANOVA with Tukey’s post hoc test; **** P < 0.0001.

    Article Snippet: ACHN and A498 human renal adenocarcinomas (ATCC) and ONCO-DG-1 human ovarian adenocarcinomas (DSMZ) were cultivated in Roswell Park Memorial Institute (RPMI) 1640 medium (Gibco).

    Techniques: Imaging, Fluorescence, Incubation

    Fig. 2 HHLA2 expression is induced on A498 ccRCC cell line in vivo. A Expression of HHLA2 on A498 cells in vitro. B-G Five million A498 or 786-O cells were injected subcutaneously into NSG mice and tumors were harvested at a size of at least 10 mm. HHLA2 expression was analyzed by (B) flow cytometry on day 0 and after 1, 4, and 7 days of culture in vitro (numbers in upper right indicate % HHLA2 positive) and (C) by immunohistochemistry on day 0. D-G representative H&E and HHLA2 images of A498 and 786-O tumors, respectively. The statistical significance of difference versus control cells is indicated as ****p < 0.0001

    Journal: BMC cancer

    Article Title: Regulation of HHLA2 expression in kidney cancer and myeloid cells.

    doi: 10.1186/s12885-023-11496-9

    Figure Lengend Snippet: Fig. 2 HHLA2 expression is induced on A498 ccRCC cell line in vivo. A Expression of HHLA2 on A498 cells in vitro. B-G Five million A498 or 786-O cells were injected subcutaneously into NSG mice and tumors were harvested at a size of at least 10 mm. HHLA2 expression was analyzed by (B) flow cytometry on day 0 and after 1, 4, and 7 days of culture in vitro (numbers in upper right indicate % HHLA2 positive) and (C) by immunohistochemistry on day 0. D-G representative H&E and HHLA2 images of A498 and 786-O tumors, respectively. The statistical significance of difference versus control cells is indicated as ****p < 0.0001

    Article Snippet: Human renal adenocarcinoma cell lines A498 and 786-O, human lung adenocarcinoma cell line A549 and human breast cancer cell line MCF7 were purchased from the ATCC.

    Techniques: Expressing, In Vivo, In Vitro, Injection, Flow Cytometry, Immunohistochemistry, Control