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Pasteur Institute mcf 7 human breast cancer cell line
Cytotoxic effect of compounds 5a-5e <t>on</t> <t>MCF-7</t> cells following exposure to different concentrations (10, 20, 60, and 100 μM). Data are presented as mean ± SD, n = 3. *P < 0.05, **P < 0.01, and *** P < 0.001 indicate significant differences in comparison with the negative control group (untreated cells); doxorubicin was used as the positive control.
Mcf 7 Human Breast Cancer Cell Line, supplied by Pasteur Institute, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/human+breast+cancer+cell+line+mcf/pmc13268006-48-1-11?v=Pasteur+Institute
Average 86 stars, based on 1 article reviews
mcf 7 human breast cancer cell line - by Bioz Stars, 2026-08
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Article Title: Molecular docking, synthesis, and cytotoxic evaluation of novel quinazoline-quinazolinone hybrid compounds

Journal: Research in Pharmaceutical Sciences

doi: 10.4103/RPS.RPS_150_24

Cytotoxic effect of compounds 5a-5e on MCF-7 cells following exposure to different concentrations (10, 20, 60, and 100 μM). Data are presented as mean ± SD, n = 3. *P < 0.05, **P < 0.01, and *** P < 0.001 indicate significant differences in comparison with the negative control group (untreated cells); doxorubicin was used as the positive control.
Figure Legend Snippet: Cytotoxic effect of compounds 5a-5e on MCF-7 cells following exposure to different concentrations (10, 20, 60, and 100 μM). Data are presented as mean ± SD, n = 3. *P < 0.05, **P < 0.01, and *** P < 0.001 indicate significant differences in comparison with the negative control group (untreated cells); doxorubicin was used as the positive control.

Techniques Used: Comparison, Negative Control, Positive Control



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Cytotoxic effect of compounds 5a-5e on MCF-7 cells following exposure to different concentrations (10, 20, 60, and 100 μM). Data are presented as mean ± SD, n = 3. *P < 0.05, **P < 0.01, and *** P < 0.001 indicate significant differences in comparison with the negative control group (untreated cells); doxorubicin was used as the positive control.

Journal: Research in Pharmaceutical Sciences

Article Title: Molecular docking, synthesis, and cytotoxic evaluation of novel quinazoline-quinazolinone hybrid compounds

doi: 10.4103/RPS.RPS_150_24

Figure Lengend Snippet: Cytotoxic effect of compounds 5a-5e on MCF-7 cells following exposure to different concentrations (10, 20, 60, and 100 μM). Data are presented as mean ± SD, n = 3. *P < 0.05, **P < 0.01, and *** P < 0.001 indicate significant differences in comparison with the negative control group (untreated cells); doxorubicin was used as the positive control.

Article Snippet: The MCF-7 (human breast cancer) cell line was acquired from the Pasteur Institute of Iran (Tehran, Iran).

Techniques: Comparison, Negative Control, Positive Control

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