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ec cell lines  (ATCC)


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    Structured Review

    ATCC ec cell lines
    Ec Cell Lines, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 441 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/ec cell lines/product/ATCC
    Average 96 stars, based on 441 article reviews
    ec cell lines - by Bioz Stars, 2026-05
    96/100 stars

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    Genechem human ec cell lines hec 1 a
    DEP inhibited proliferation and induced ROS accumulation in EC cells. ( A , B ) CCK-8 assay showing the effect of different concentrations of DEP on <t>proliferation</t> <t>of</t> <t>HEC-1-A</t> ( A ) and Ishikawa ( B ) cells at 0, 24, and 48 h (n = 3). ( C , D ) Representative EdU staining images of HEC-1-A ( C ) and Ishikawa ( D ) cells treated with DEP at the indicated concentrations (DMSO, DEP at 10 nM, 1 μM, and 10 μM). Nuclei were counterstained with Hoechst 33,342 (blue), and EdU-positive cells are shown in red. Scale bar = 100 μm. ( E ) Quantification of EdU-positive cells in HEC-1-A and Ishikawa cell lines (n = 3). ( F ) Representative fluorescence images of ROS staining in HEC-1-A and Ishikawa cells following DEP treatment. White arrows indicate cells with increased ROS levels, and blue arrows indicate cells with lower ROS levels (n = 3). Scale bar = 20 μm. Data are presented as mean ± SD; statistical significance was determined by one-way ANOVA followed by Tukey’s post hoc test. (* P < 0.05, *** P < 0.001, **** P < 0.0001).
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    DEP inhibited proliferation and induced ROS accumulation in EC cells. ( A , B ) CCK-8 assay showing the effect of different concentrations of DEP on proliferation of HEC-1-A ( A ) and Ishikawa ( B ) cells at 0, 24, and 48 h (n = 3). ( C , D ) Representative EdU staining images of HEC-1-A ( C ) and Ishikawa ( D ) cells treated with DEP at the indicated concentrations (DMSO, DEP at 10 nM, 1 μM, and 10 μM). Nuclei were counterstained with Hoechst 33,342 (blue), and EdU-positive cells are shown in red. Scale bar = 100 μm. ( E ) Quantification of EdU-positive cells in HEC-1-A and Ishikawa cell lines (n = 3). ( F ) Representative fluorescence images of ROS staining in HEC-1-A and Ishikawa cells following DEP treatment. White arrows indicate cells with increased ROS levels, and blue arrows indicate cells with lower ROS levels (n = 3). Scale bar = 20 μm. Data are presented as mean ± SD; statistical significance was determined by one-way ANOVA followed by Tukey’s post hoc test. (* P < 0.05, *** P < 0.001, **** P < 0.0001).

    Journal: Scientific Reports

    Article Title: Integrative network toxicology and experimental evidence reveal mechanisms underlying diethyl phthalate-induced initiation and progression of endometrial cancer

    doi: 10.1038/s41598-026-39325-6

    Figure Lengend Snippet: DEP inhibited proliferation and induced ROS accumulation in EC cells. ( A , B ) CCK-8 assay showing the effect of different concentrations of DEP on proliferation of HEC-1-A ( A ) and Ishikawa ( B ) cells at 0, 24, and 48 h (n = 3). ( C , D ) Representative EdU staining images of HEC-1-A ( C ) and Ishikawa ( D ) cells treated with DEP at the indicated concentrations (DMSO, DEP at 10 nM, 1 μM, and 10 μM). Nuclei were counterstained with Hoechst 33,342 (blue), and EdU-positive cells are shown in red. Scale bar = 100 μm. ( E ) Quantification of EdU-positive cells in HEC-1-A and Ishikawa cell lines (n = 3). ( F ) Representative fluorescence images of ROS staining in HEC-1-A and Ishikawa cells following DEP treatment. White arrows indicate cells with increased ROS levels, and blue arrows indicate cells with lower ROS levels (n = 3). Scale bar = 20 μm. Data are presented as mean ± SD; statistical significance was determined by one-way ANOVA followed by Tukey’s post hoc test. (* P < 0.05, *** P < 0.001, **** P < 0.0001).

    Article Snippet: The human EC cell lines HEC-1-A and Ishikawa were obtained from GeneChem Gene Technology Co., Ltd. (Shanghai, China).

    Techniques: CCK-8 Assay, Staining, Fluorescence

    DEP induced cell cycle arrest and modulated the PI3K/AKT signaling pathway in EC cells. ( A ) Flow cytometry analysis of cell cycle distribution in Ishikawa and HEC-1-A cells treated with DEP at the indicated concentrations (DMSO, DEP at 10 nM, 1 μM, and 10 μM). ( B ) Quantification of the proportion of cells in G0/G1, S, and G2/M phases (n = 3). ( C ) WB analysis of PI3K, P-PI3K, AKT, P-AKT, ERK, P-ERK, CDK4, Cyclin D1, GSK3β, and P-GSK3β expression in Ishikawa and HEC-1-A cells after DEP treatment. ( D ) Densitometric quantification of protein expression levels normalized to GAPDH or β-actin (n = 3). Data are presented as mean ± SD; statistical significance was determined by one-way ANOVA followed by Tukey’s post hoc test. (ns = not significant, * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001).

    Journal: Scientific Reports

    Article Title: Integrative network toxicology and experimental evidence reveal mechanisms underlying diethyl phthalate-induced initiation and progression of endometrial cancer

    doi: 10.1038/s41598-026-39325-6

    Figure Lengend Snippet: DEP induced cell cycle arrest and modulated the PI3K/AKT signaling pathway in EC cells. ( A ) Flow cytometry analysis of cell cycle distribution in Ishikawa and HEC-1-A cells treated with DEP at the indicated concentrations (DMSO, DEP at 10 nM, 1 μM, and 10 μM). ( B ) Quantification of the proportion of cells in G0/G1, S, and G2/M phases (n = 3). ( C ) WB analysis of PI3K, P-PI3K, AKT, P-AKT, ERK, P-ERK, CDK4, Cyclin D1, GSK3β, and P-GSK3β expression in Ishikawa and HEC-1-A cells after DEP treatment. ( D ) Densitometric quantification of protein expression levels normalized to GAPDH or β-actin (n = 3). Data are presented as mean ± SD; statistical significance was determined by one-way ANOVA followed by Tukey’s post hoc test. (ns = not significant, * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001).

    Article Snippet: The human EC cell lines HEC-1-A and Ishikawa were obtained from GeneChem Gene Technology Co., Ltd. (Shanghai, China).

    Techniques: Flow Cytometry, Expressing