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ct26 murine colorectal carcinoma cell line  (ATCC)


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    Structured Review

    ATCC ct26 murine colorectal carcinoma cell line
    Combination RT and anti-CCR8 reduces tumor burden and improve survival in distant non-irradiated tumors BALB/c mice were injected with <t>CT26</t> on both flanks. Tumor-bearing mice were treated with a “pre” treatment strategy. Mice were injected i.p. with anti-CCR8 on days 7, 10, and 14 and treated with 12 Gy RT to the right flank tumor (treated) on day14 post-tumor inoculation. The left tumor (untreated) did not receive RT. Tumor growth and survival were assessed. A total of 8 mice were analyzed per group. Data are represented as mean ± SD. Statistics for survival plots were performed using a Mantel-Cox test between groups. ns = not significant, ∗∗∗∗ p < 0.0001, ∗∗∗ p < 0.001, ∗∗ p < 0.01, ∗ p < 0.05.
    Ct26 Murine Colorectal Carcinoma Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 3500 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/ct26 murine colorectal carcinoma cell line/product/ATCC
    Average 99 stars, based on 3500 article reviews
    ct26 murine colorectal carcinoma cell line - by Bioz Stars, 2026-02
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    Images

    1) Product Images from "Fluorescence tracking Treg movement identifies anti-CCR8 and radiation as a therapeutic combination"

    Article Title: Fluorescence tracking Treg movement identifies anti-CCR8 and radiation as a therapeutic combination

    Journal: iScience

    doi: 10.1016/j.isci.2025.114572

    Combination RT and anti-CCR8 reduces tumor burden and improve survival in distant non-irradiated tumors BALB/c mice were injected with CT26 on both flanks. Tumor-bearing mice were treated with a “pre” treatment strategy. Mice were injected i.p. with anti-CCR8 on days 7, 10, and 14 and treated with 12 Gy RT to the right flank tumor (treated) on day14 post-tumor inoculation. The left tumor (untreated) did not receive RT. Tumor growth and survival were assessed. A total of 8 mice were analyzed per group. Data are represented as mean ± SD. Statistics for survival plots were performed using a Mantel-Cox test between groups. ns = not significant, ∗∗∗∗ p < 0.0001, ∗∗∗ p < 0.001, ∗∗ p < 0.01, ∗ p < 0.05.
    Figure Legend Snippet: Combination RT and anti-CCR8 reduces tumor burden and improve survival in distant non-irradiated tumors BALB/c mice were injected with CT26 on both flanks. Tumor-bearing mice were treated with a “pre” treatment strategy. Mice were injected i.p. with anti-CCR8 on days 7, 10, and 14 and treated with 12 Gy RT to the right flank tumor (treated) on day14 post-tumor inoculation. The left tumor (untreated) did not receive RT. Tumor growth and survival were assessed. A total of 8 mice were analyzed per group. Data are represented as mean ± SD. Statistics for survival plots were performed using a Mantel-Cox test between groups. ns = not significant, ∗∗∗∗ p < 0.0001, ∗∗∗ p < 0.001, ∗∗ p < 0.01, ∗ p < 0.05.

    Techniques Used: Irradiation, Injection



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    Image Search Results


    Combination RT and anti-CCR8 reduces tumor burden and improve survival in distant non-irradiated tumors BALB/c mice were injected with CT26 on both flanks. Tumor-bearing mice were treated with a “pre” treatment strategy. Mice were injected i.p. with anti-CCR8 on days 7, 10, and 14 and treated with 12 Gy RT to the right flank tumor (treated) on day14 post-tumor inoculation. The left tumor (untreated) did not receive RT. Tumor growth and survival were assessed. A total of 8 mice were analyzed per group. Data are represented as mean ± SD. Statistics for survival plots were performed using a Mantel-Cox test between groups. ns = not significant, ∗∗∗∗ p < 0.0001, ∗∗∗ p < 0.001, ∗∗ p < 0.01, ∗ p < 0.05.

    Journal: iScience

    Article Title: Fluorescence tracking Treg movement identifies anti-CCR8 and radiation as a therapeutic combination

    doi: 10.1016/j.isci.2025.114572

    Figure Lengend Snippet: Combination RT and anti-CCR8 reduces tumor burden and improve survival in distant non-irradiated tumors BALB/c mice were injected with CT26 on both flanks. Tumor-bearing mice were treated with a “pre” treatment strategy. Mice were injected i.p. with anti-CCR8 on days 7, 10, and 14 and treated with 12 Gy RT to the right flank tumor (treated) on day14 post-tumor inoculation. The left tumor (untreated) did not receive RT. Tumor growth and survival were assessed. A total of 8 mice were analyzed per group. Data are represented as mean ± SD. Statistics for survival plots were performed using a Mantel-Cox test between groups. ns = not significant, ∗∗∗∗ p < 0.0001, ∗∗∗ p < 0.001, ∗∗ p < 0.01, ∗ p < 0.05.

    Article Snippet: The CT26 murine colorectal carcinoma cell line was purchased from ATCC (CRL-2638).

    Techniques: Irradiation, Injection

    Intrinsic sensitivity of tumor cells to ECT in vitro. Intrinsic sensitivity of WEHI fibrosarcoma ( a ), CT26 colorectal carcinoma ( b ), 4T1 mammary carcinoma ( c ) and MC38 colorectal carcinoma ( d ) with corresponding IC50 values ( e ). * p < 0.05 indicates a significant difference compared to untreated control or EP group ( a – d ). ** p < 0.05 indicates a significant difference between indicated cell lines ( e ).

    Journal: Cancers

    Article Title: Potentiation of Electrochemotherapy by Anti-PD-1 Immunotherapy in Murine Tumors with Distinct Immune Profiles

    doi: 10.3390/cancers18010090

    Figure Lengend Snippet: Intrinsic sensitivity of tumor cells to ECT in vitro. Intrinsic sensitivity of WEHI fibrosarcoma ( a ), CT26 colorectal carcinoma ( b ), 4T1 mammary carcinoma ( c ) and MC38 colorectal carcinoma ( d ) with corresponding IC50 values ( e ). * p < 0.05 indicates a significant difference compared to untreated control or EP group ( a – d ). ** p < 0.05 indicates a significant difference between indicated cell lines ( e ).

    Article Snippet: Mammary carcinoma 4T1 cells, murine fibrosarcoma WEHI cells, and murine colorectal carcinoma CT26 cells (all from the American Type Culture Collection, Manassas, VA, USA) were cultured in Advanced RPMI-1640 medium (Gibco, Waltham, MA, USA).

    Techniques: In Vitro, Control

    Effectiveness of ECT in murine tumors. Growth curves of WEHI fibrosarcoma ( a ), CT26 colorectal carcinoma ( b ), 4T1 mammary carcinoma ( c ) and MC38 colorectal carcinoma ( d ) are presented as AM ± SE. cr = complete response, mice with cured tumors, number of animals = 12 in all other groups, then ECT. EP = electroporation, BLM = bleomycin, ECT = electrochemotherapy.

    Journal: Cancers

    Article Title: Potentiation of Electrochemotherapy by Anti-PD-1 Immunotherapy in Murine Tumors with Distinct Immune Profiles

    doi: 10.3390/cancers18010090

    Figure Lengend Snippet: Effectiveness of ECT in murine tumors. Growth curves of WEHI fibrosarcoma ( a ), CT26 colorectal carcinoma ( b ), 4T1 mammary carcinoma ( c ) and MC38 colorectal carcinoma ( d ) are presented as AM ± SE. cr = complete response, mice with cured tumors, number of animals = 12 in all other groups, then ECT. EP = electroporation, BLM = bleomycin, ECT = electrochemotherapy.

    Article Snippet: Mammary carcinoma 4T1 cells, murine fibrosarcoma WEHI cells, and murine colorectal carcinoma CT26 cells (all from the American Type Culture Collection, Manassas, VA, USA) were cultured in Advanced RPMI-1640 medium (Gibco, Waltham, MA, USA).

    Techniques: Electroporation

    Effectiveness of anti-PD-1 immunotherapy in murine tumors. Growth curves of WEHI fibrosarcoma ( a ), CT26 colorectal carcinoma ( b ), 4T1 mammary carcinoma ( c ) and MC38 colorectal carcinoma ( d ) are presented as AM ± SE. number of animals = 12 in all groups.

    Journal: Cancers

    Article Title: Potentiation of Electrochemotherapy by Anti-PD-1 Immunotherapy in Murine Tumors with Distinct Immune Profiles

    doi: 10.3390/cancers18010090

    Figure Lengend Snippet: Effectiveness of anti-PD-1 immunotherapy in murine tumors. Growth curves of WEHI fibrosarcoma ( a ), CT26 colorectal carcinoma ( b ), 4T1 mammary carcinoma ( c ) and MC38 colorectal carcinoma ( d ) are presented as AM ± SE. number of animals = 12 in all groups.

    Article Snippet: Mammary carcinoma 4T1 cells, murine fibrosarcoma WEHI cells, and murine colorectal carcinoma CT26 cells (all from the American Type Culture Collection, Manassas, VA, USA) were cultured in Advanced RPMI-1640 medium (Gibco, Waltham, MA, USA).

    Techniques:

    Effectiveness of combined ECT + anti-PD-1 treatment. Growth curves of CT26 colorectal carcinoma ( a ), 4T1 mammary carcinoma ( b ) and MC38 colorectal carcinoma ( c ) are presented as AM ± SE. CR = complete response, mice with cured tumors, number of animals = 15 in all other groups, then ECT + anti-PD-1. ECT = electrochemotherapy, BLM = bleomycin, ECT = electrochemotherapy.

    Journal: Cancers

    Article Title: Potentiation of Electrochemotherapy by Anti-PD-1 Immunotherapy in Murine Tumors with Distinct Immune Profiles

    doi: 10.3390/cancers18010090

    Figure Lengend Snippet: Effectiveness of combined ECT + anti-PD-1 treatment. Growth curves of CT26 colorectal carcinoma ( a ), 4T1 mammary carcinoma ( b ) and MC38 colorectal carcinoma ( c ) are presented as AM ± SE. CR = complete response, mice with cured tumors, number of animals = 15 in all other groups, then ECT + anti-PD-1. ECT = electrochemotherapy, BLM = bleomycin, ECT = electrochemotherapy.

    Article Snippet: Mammary carcinoma 4T1 cells, murine fibrosarcoma WEHI cells, and murine colorectal carcinoma CT26 cells (all from the American Type Culture Collection, Manassas, VA, USA) were cultured in Advanced RPMI-1640 medium (Gibco, Waltham, MA, USA).

    Techniques: