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human breast cancer cell line mcf 7  (ATCC)


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    ATCC human breast cancer cell line mcf 7
    Human Breast Cancer Cell Line Mcf 7, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 34296 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mcf7+human+breast+cancer+cell+line/pmc13101642-243-7-13?v=ATCC
    Average 99 stars, based on 34296 article reviews
    human breast cancer cell line mcf 7 - by Bioz Stars, 2026-07
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    ATCC human breast cancer cell line mcf 7
    Human Breast Cancer Cell Line Mcf 7, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC human er positive breast cancer cell lines mcf 7
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    ATCC human breast cancer cell lines mcf 7
    Zoledronic Acid Induces Ferroptosis in ER+ Breast Cancer Cells. (A) Dose-dependent growth inhibition by zoledronic acid <t>(ZA).</t> <t>MCF-7</t> and ZR-75-1 cells were treated with increasing ZA concentrations (0-80 μM) for 72 h, followed by CCK-8 viability assays. (B) Intracellular iron accumulation quantified by colorimetric assay. Cells exposed to 40 μM ZA for 24 h showed elevated iron levels. (C, D) ZA-induced lipid peroxidation in MCF-7 (C) and ZR-75-1 (D) was detected by flow cytometry. Cells treated with 40 μM ZA for 24 h exhibited increased BODIPY 581/591 C11 oxidation. ** p <0.01; *** p <0.001.
    Human Breast Cancer Cell Lines Mcf 7, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC mcf7 human breast cancer cell line
    Zoledronic Acid Induces Ferroptosis in ER+ Breast Cancer Cells. (A) Dose-dependent growth inhibition by zoledronic acid <t>(ZA).</t> <t>MCF-7</t> and ZR-75-1 cells were treated with increasing ZA concentrations (0-80 μM) for 72 h, followed by CCK-8 viability assays. (B) Intracellular iron accumulation quantified by colorimetric assay. Cells exposed to 40 μM ZA for 24 h showed elevated iron levels. (C, D) ZA-induced lipid peroxidation in MCF-7 (C) and ZR-75-1 (D) was detected by flow cytometry. Cells treated with 40 μM ZA for 24 h exhibited increased BODIPY 581/591 C11 oxidation. ** p <0.01; *** p <0.001.
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    Zoledronic Acid Induces Ferroptosis in ER+ Breast Cancer Cells. (A) Dose-dependent growth inhibition by zoledronic acid <t>(ZA).</t> <t>MCF-7</t> and ZR-75-1 cells were treated with increasing ZA concentrations (0-80 μM) for 72 h, followed by CCK-8 viability assays. (B) Intracellular iron accumulation quantified by colorimetric assay. Cells exposed to 40 μM ZA for 24 h showed elevated iron levels. (C, D) ZA-induced lipid peroxidation in MCF-7 (C) and ZR-75-1 (D) was detected by flow cytometry. Cells treated with 40 μM ZA for 24 h exhibited increased BODIPY 581/591 C11 oxidation. ** p <0.01; *** p <0.001.
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    ATCC human breast cancer cell lines mcf7
    Zoledronic Acid Induces Ferroptosis in ER+ Breast Cancer Cells. (A) Dose-dependent growth inhibition by zoledronic acid <t>(ZA).</t> <t>MCF-7</t> and ZR-75-1 cells were treated with increasing ZA concentrations (0-80 μM) for 72 h, followed by CCK-8 viability assays. (B) Intracellular iron accumulation quantified by colorimetric assay. Cells exposed to 40 μM ZA for 24 h showed elevated iron levels. (C, D) ZA-induced lipid peroxidation in MCF-7 (C) and ZR-75-1 (D) was detected by flow cytometry. Cells treated with 40 μM ZA for 24 h exhibited increased BODIPY 581/591 C11 oxidation. ** p <0.01; *** p <0.001.
    Human Breast Cancer Cell Lines Mcf7, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mcf7+human+breast+cancer+cell+line/pm42025940-59-0-19?v=ATCC
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    human breast cancer cell lines mcf7 - by Bioz Stars, 2026-07
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    ATCC human breast cancer cell line mcf7
    (A): Cell binding, cell internalization and surface bound–[ 186 Re]Re-(htbh) 2 in <t>MCF7</t> and Vero cell line; (B): MTT-based Cytotoxicity of H(htbh) and [ 186 Re]Re-(htbh) 2 in MCF7 and Vero cell line, showing comparative cell viability following pulsed treatment; Flow Cytometry-based detection of percentage sub G1 or dead cell population (DC) in (C): Control MCF 7 cells; and in treatment groups including (D): H(htbh); (E): [ 186 Re]Re-(htbh) 2 –Group 1; (F): [ 186 Re]Re-(htbh) 2 –Group 2. (G): Setting for live and dead cell selection using FSC and SSC plot; and (H): histogram showing percentage of dead cell population (DC) in different treatment groups.
    Human Breast Cancer Cell Line Mcf7, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC human breast cell line culture cancerous mcf 7
    (A): Cell binding, cell internalization and surface bound–[ 186 Re]Re-(htbh) 2 in <t>MCF7</t> and Vero cell line; (B): MTT-based Cytotoxicity of H(htbh) and [ 186 Re]Re-(htbh) 2 in MCF7 and Vero cell line, showing comparative cell viability following pulsed treatment; Flow Cytometry-based detection of percentage sub G1 or dead cell population (DC) in (C): Control MCF 7 cells; and in treatment groups including (D): H(htbh); (E): [ 186 Re]Re-(htbh) 2 –Group 1; (F): [ 186 Re]Re-(htbh) 2 –Group 2. (G): Setting for live and dead cell selection using FSC and SSC plot; and (H): histogram showing percentage of dead cell population (DC) in different treatment groups.
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    Zoledronic Acid Induces Ferroptosis in ER+ Breast Cancer Cells. (A) Dose-dependent growth inhibition by zoledronic acid (ZA). MCF-7 and ZR-75-1 cells were treated with increasing ZA concentrations (0-80 μM) for 72 h, followed by CCK-8 viability assays. (B) Intracellular iron accumulation quantified by colorimetric assay. Cells exposed to 40 μM ZA for 24 h showed elevated iron levels. (C, D) ZA-induced lipid peroxidation in MCF-7 (C) and ZR-75-1 (D) was detected by flow cytometry. Cells treated with 40 μM ZA for 24 h exhibited increased BODIPY 581/591 C11 oxidation. ** p <0.01; *** p <0.001.

    Journal: Biomolecules & Therapeutics

    Article Title: Zoledronic Acid Inhibits the Growth of ER-Positive Breast Cancer Cells by Inducing Ferroptosis

    doi: 10.4062/biomolther.2025.132

    Figure Lengend Snippet: Zoledronic Acid Induces Ferroptosis in ER+ Breast Cancer Cells. (A) Dose-dependent growth inhibition by zoledronic acid (ZA). MCF-7 and ZR-75-1 cells were treated with increasing ZA concentrations (0-80 μM) for 72 h, followed by CCK-8 viability assays. (B) Intracellular iron accumulation quantified by colorimetric assay. Cells exposed to 40 μM ZA for 24 h showed elevated iron levels. (C, D) ZA-induced lipid peroxidation in MCF-7 (C) and ZR-75-1 (D) was detected by flow cytometry. Cells treated with 40 μM ZA for 24 h exhibited increased BODIPY 581/591 C11 oxidation. ** p <0.01; *** p <0.001.

    Article Snippet: Human breast cancer cell lines MCF-7 (ATCC ® HTB-22TM), ZR-75-1 (ATCC ® CRL-1500TM), HCC1954, MDA-MB-231, and HEK293T-17 were obtained from the American Type Culture Collection (ATCC, MD, USA).

    Techniques: Inhibition, CCK-8 Assay, Colorimetric Assay, Flow Cytometry

    Ferrostatin-1 Attenuates ZA-Induced Ferroptosis. (A, B) Lipid ROS suppression by ferroptosis inhibition. Co-treatment with 5 μM Ferrostatin-1 (Ferro-1) partially reversed ZA-induced BODIPY 581/591 C11 oxidation in MCF-7 (A) and ZR-75-1 (B). (C) Viability rescue by Ferro-1. CCK-8 assays demonstrated partial recovery of cell growth in ZA (40 μM)+Ferro-1 (5 μM) co-treated groups after 48 h. * p <0.05; ** p <0.01; *** p <0.001.

    Journal: Biomolecules & Therapeutics

    Article Title: Zoledronic Acid Inhibits the Growth of ER-Positive Breast Cancer Cells by Inducing Ferroptosis

    doi: 10.4062/biomolther.2025.132

    Figure Lengend Snippet: Ferrostatin-1 Attenuates ZA-Induced Ferroptosis. (A, B) Lipid ROS suppression by ferroptosis inhibition. Co-treatment with 5 μM Ferrostatin-1 (Ferro-1) partially reversed ZA-induced BODIPY 581/591 C11 oxidation in MCF-7 (A) and ZR-75-1 (B). (C) Viability rescue by Ferro-1. CCK-8 assays demonstrated partial recovery of cell growth in ZA (40 μM)+Ferro-1 (5 μM) co-treated groups after 48 h. * p <0.05; ** p <0.01; *** p <0.001.

    Article Snippet: Human breast cancer cell lines MCF-7 (ATCC ® HTB-22TM), ZR-75-1 (ATCC ® CRL-1500TM), HCC1954, MDA-MB-231, and HEK293T-17 were obtained from the American Type Culture Collection (ATCC, MD, USA).

    Techniques: Inhibition, CCK-8 Assay

    Synergistic Ferroptosis Induction by ZA and RSL3. (A, B) Enhanced lipid peroxidation with combination therapy. RSL3 (5 μM) potentiated ZA-induced BODIPY 581/591 C11 oxidation in MCF-7 (A) and ZR-75-1 (B). (C) Cooperative growth inhibition. Crystal violet colony formation assay demonstrated ZA (40 μM)+RSL3 (5 μM) co-treatment for 6 days showed enhanced cytotoxicity compared to single agents. * p <0.05; ** p <0.01; *** p <0.001.

    Journal: Biomolecules & Therapeutics

    Article Title: Zoledronic Acid Inhibits the Growth of ER-Positive Breast Cancer Cells by Inducing Ferroptosis

    doi: 10.4062/biomolther.2025.132

    Figure Lengend Snippet: Synergistic Ferroptosis Induction by ZA and RSL3. (A, B) Enhanced lipid peroxidation with combination therapy. RSL3 (5 μM) potentiated ZA-induced BODIPY 581/591 C11 oxidation in MCF-7 (A) and ZR-75-1 (B). (C) Cooperative growth inhibition. Crystal violet colony formation assay demonstrated ZA (40 μM)+RSL3 (5 μM) co-treatment for 6 days showed enhanced cytotoxicity compared to single agents. * p <0.05; ** p <0.01; *** p <0.001.

    Article Snippet: Human breast cancer cell lines MCF-7 (ATCC ® HTB-22TM), ZR-75-1 (ATCC ® CRL-1500TM), HCC1954, MDA-MB-231, and HEK293T-17 were obtained from the American Type Culture Collection (ATCC, MD, USA).

    Techniques: Inhibition, Colony Assay

    ZA Downregulates Ferroptosis Suppressors SLC7A11 and GPX4. (A, B) Dose-dependent protein suppression. Western blot analysis revealed decreased SLC7A11 and GPX4 expression in MCF-7 (A) and ZR-75-1 (B) after 24 h ZA treatment (20-40 μM). Tubulin served as loading control.

    Journal: Biomolecules & Therapeutics

    Article Title: Zoledronic Acid Inhibits the Growth of ER-Positive Breast Cancer Cells by Inducing Ferroptosis

    doi: 10.4062/biomolther.2025.132

    Figure Lengend Snippet: ZA Downregulates Ferroptosis Suppressors SLC7A11 and GPX4. (A, B) Dose-dependent protein suppression. Western blot analysis revealed decreased SLC7A11 and GPX4 expression in MCF-7 (A) and ZR-75-1 (B) after 24 h ZA treatment (20-40 μM). Tubulin served as loading control.

    Article Snippet: Human breast cancer cell lines MCF-7 (ATCC ® HTB-22TM), ZR-75-1 (ATCC ® CRL-1500TM), HCC1954, MDA-MB-231, and HEK293T-17 were obtained from the American Type Culture Collection (ATCC, MD, USA).

    Techniques: Western Blot, Expressing, Control

    ZA Activates Hippo Signaling Through YAP Regulation. (A) Phospho-YAP induction and total YAP reduction. Dose-responsive YAP phosphorylation and protein degradation in cells treated with ZA (20-40 μM) for 24 h. (B, C) Transcriptional downregulation of YAP targets. qRT-PCR showed decreased CTGF (B) and CYR61 (C) mRNA levels post-ZA treatment. (D) Accelerated YAP protein turnover. Cycloheximide (10 μM) chase assay demonstrated enhanced YAP degradation kinetics in MCF-7 cells pre-treated with 40 μM ZA. (E) YAP nuclear export. Immunofluorescence revealed dose-dependent reduction of nuclear YAP (green) in ZA-treated MCF-7 cells (8 h). Hoechst (blue) marks nuclei. Scale bar: 20 μm. ** p <0.01; *** p <0.001; ns: no significance.

    Journal: Biomolecules & Therapeutics

    Article Title: Zoledronic Acid Inhibits the Growth of ER-Positive Breast Cancer Cells by Inducing Ferroptosis

    doi: 10.4062/biomolther.2025.132

    Figure Lengend Snippet: ZA Activates Hippo Signaling Through YAP Regulation. (A) Phospho-YAP induction and total YAP reduction. Dose-responsive YAP phosphorylation and protein degradation in cells treated with ZA (20-40 μM) for 24 h. (B, C) Transcriptional downregulation of YAP targets. qRT-PCR showed decreased CTGF (B) and CYR61 (C) mRNA levels post-ZA treatment. (D) Accelerated YAP protein turnover. Cycloheximide (10 μM) chase assay demonstrated enhanced YAP degradation kinetics in MCF-7 cells pre-treated with 40 μM ZA. (E) YAP nuclear export. Immunofluorescence revealed dose-dependent reduction of nuclear YAP (green) in ZA-treated MCF-7 cells (8 h). Hoechst (blue) marks nuclei. Scale bar: 20 μm. ** p <0.01; *** p <0.001; ns: no significance.

    Article Snippet: Human breast cancer cell lines MCF-7 (ATCC ® HTB-22TM), ZR-75-1 (ATCC ® CRL-1500TM), HCC1954, MDA-MB-231, and HEK293T-17 were obtained from the American Type Culture Collection (ATCC, MD, USA).

    Techniques: Phospho-proteomics, Quantitative RT-PCR, Immunofluorescence

    (A): Cell binding, cell internalization and surface bound–[ 186 Re]Re-(htbh) 2 in MCF7 and Vero cell line; (B): MTT-based Cytotoxicity of H(htbh) and [ 186 Re]Re-(htbh) 2 in MCF7 and Vero cell line, showing comparative cell viability following pulsed treatment; Flow Cytometry-based detection of percentage sub G1 or dead cell population (DC) in (C): Control MCF 7 cells; and in treatment groups including (D): H(htbh); (E): [ 186 Re]Re-(htbh) 2 –Group 1; (F): [ 186 Re]Re-(htbh) 2 –Group 2. (G): Setting for live and dead cell selection using FSC and SSC plot; and (H): histogram showing percentage of dead cell population (DC) in different treatment groups.

    Journal: RSC Advances

    Article Title: Rhenium-186-labeled ortho -hydroxythiobenzhydrazide: a potential theranostic agent for use in metastatic breast cancer

    doi: 10.1039/d5ra07970e

    Figure Lengend Snippet: (A): Cell binding, cell internalization and surface bound–[ 186 Re]Re-(htbh) 2 in MCF7 and Vero cell line; (B): MTT-based Cytotoxicity of H(htbh) and [ 186 Re]Re-(htbh) 2 in MCF7 and Vero cell line, showing comparative cell viability following pulsed treatment; Flow Cytometry-based detection of percentage sub G1 or dead cell population (DC) in (C): Control MCF 7 cells; and in treatment groups including (D): H(htbh); (E): [ 186 Re]Re-(htbh) 2 –Group 1; (F): [ 186 Re]Re-(htbh) 2 –Group 2. (G): Setting for live and dead cell selection using FSC and SSC plot; and (H): histogram showing percentage of dead cell population (DC) in different treatment groups.

    Article Snippet: Human breast cancer cell line MCF7 (ATCC®, HTB-22TM) was used for in-vitro cell binding study for the evaluation of [ 186 Re]Re-(htbh) 2 complex.

    Techniques: Binding Assay, Flow Cytometry, Control, Selection

    (A): Biodistribution of [ 186 Re]Re-(htbh) 2 in MCF-7 tumour xenografted female SCID mice; (B): tumour to organ ratio, 2 h post injection; (C and D): SPECT/CT images of female SCID mice with MCF7 tumour xenograft.

    Journal: RSC Advances

    Article Title: Rhenium-186-labeled ortho -hydroxythiobenzhydrazide: a potential theranostic agent for use in metastatic breast cancer

    doi: 10.1039/d5ra07970e

    Figure Lengend Snippet: (A): Biodistribution of [ 186 Re]Re-(htbh) 2 in MCF-7 tumour xenografted female SCID mice; (B): tumour to organ ratio, 2 h post injection; (C and D): SPECT/CT images of female SCID mice with MCF7 tumour xenograft.

    Article Snippet: Human breast cancer cell line MCF7 (ATCC®, HTB-22TM) was used for in-vitro cell binding study for the evaluation of [ 186 Re]Re-(htbh) 2 complex.

    Techniques: Injection, Single Photon Emission Computed Tomography