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human luminal a breast cancer cells  (ATCC)


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    ATCC human luminal a breast cancer cells
    Human Luminal A Breast Cancer Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 34837 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mcf7+luminal+breast+cancer+cells/MCF7/10__3390_slash_metabo16060349-52-0-7
    Average 99 stars, based on 34837 article reviews
    human luminal a breast cancer cells - by Bioz Stars, 2026-09
    99/100 stars

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    Multiple Displacement Amplification:

    Article Title: 18-20 member bi-polycyclic compounds
    Article Snippet: .. The cytotoxicity of compounds was examined and directly compared to compound 17, by measuring cell survival of clonal tumor cell lines IMR-32, BE2C (neuroblastoma), as well as MDA-MB-231, BT20, HCC-38 (Basal) and MCF7 (luminal) breast cancer cells (ATCC). ..

    Article Title: Sorafenib analogue SC ‐60 induces apoptosis through the SHP ‐1/ STAT 3 pathway and enhances docetaxel cytotoxicity in triple‐negative breast cancer cells
    Article Snippet: Other antibodies such as poly (ADP‐ribose) polymerase (PARP) and cleaved caspase 3 were obtained from Cell Signaling Technology. .. The MCF10A human breast epithelial cell line, MCF7 luminal breast cancer cells, and TNBC (MDA‐MB‐231, MDA‐MB‐468, and HCC‐1937) cell lines were obtained from American Type Culture Collection (Manassas, VA, USA). ..

    Article Title: 18-20 member bi-polycyclic compounds
    Article Snippet: .. The cytotoxicity of compounds was examined and directly compared to compound 17, by measuring cell survival of clonal tumor cell lines IMR-32, BE2C (neuroblastoma), as well as MDA-MB-231, BT20, HCC-38 (Basal) and MCF7 (luminal) breast cancer cells (ATCC). ..

    Article Title: 18-20 member bi-polycyclic compounds
    Article Snippet: .. The cytotoxicity of compounds was examined and directly compared to compound 17, by measuring cell survival of clonal tumor cell lines IMR-32, BE2C (neuroblastoma), as well as MDA-MB-231, BT20, HCC-38 (Basal) and MCF7 (luminal) breast cancer cells (ATCC). ..

    Article Title: A genomics approach to identify susceptibilities of breast cancer cells to “fever-range” hyperthermia
    Article Snippet: .. MCF10A (ATCC #CRL10318) mammary epithelial cells and MCF7 luminal breast cancer cells (ATCC #HTB-22), MDA-MB-231 Basal B breast cancer cells (ATCC # HTB-26), and MDA-MB-468 Basal A breast cancer cells (ATCC #HTB-132) were purchased from ATCC and grown in standard culture conditions as previously reported [ - ]. ..



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    Evaluation of HG-Combination in breast cancer cell lines. MCF7 and T47D cell lines were treated with (A) ARV-471, Palbociclib, and their combination and (B) HG-ARV471, HG-Palbociclib, and HG-combination for 72 h, followed by MTT assays ( n = 3). All three replicates for each sample are represented as mean ± standard error of the mean (SEM). * p < 0.05;** p < 0.01; *** p < 0.001. (C) Synergistic studies to evaluate the effect of free combination and HG-Combination. Combination index (CI) for the different drug combinations obtained using CalcuSyn from viability values obtained in an MTT assay. CI values lower than 0.8 indicate synergistic action. * p ≤ 0.05 and ** p ≤ 0.01.

    Journal: Scientific Reports

    Article Title: Dual-drug codelivery gelatin-based hydrogel of ARV-471 and Palbociclib enhances synergistic effect in breast cancer treatment

    doi: 10.1038/s41598-025-30803-x

    Figure Lengend Snippet: Evaluation of HG-Combination in breast cancer cell lines. MCF7 and T47D cell lines were treated with (A) ARV-471, Palbociclib, and their combination and (B) HG-ARV471, HG-Palbociclib, and HG-combination for 72 h, followed by MTT assays ( n = 3). All three replicates for each sample are represented as mean ± standard error of the mean (SEM). * p < 0.05;** p < 0.01; *** p < 0.001. (C) Synergistic studies to evaluate the effect of free combination and HG-Combination. Combination index (CI) for the different drug combinations obtained using CalcuSyn from viability values obtained in an MTT assay. CI values lower than 0.8 indicate synergistic action. * p ≤ 0.05 and ** p ≤ 0.01.

    Article Snippet: Luminal breast cancer cell lines MCF7 and T47D, non-tumorigenic keratinocyte cell line HaCaT, and non-tumoral breast epithelial cell line MCF10A were purchased from ATCC (Manassas, VA, USA).

    Techniques: MTT Assay

    MCF7 and T47D seeded in Matrigel matrix and treated with the free combination, and HG-Combination at 72 h ( n = 3). The diameter of 3D structures was quantified (µm). All three replicates for each sample are represented as mean ± standard error of the mean (SEM). * p < 0.05;** p < 0.01; *** p < 0.001.

    Journal: Scientific Reports

    Article Title: Dual-drug codelivery gelatin-based hydrogel of ARV-471 and Palbociclib enhances synergistic effect in breast cancer treatment

    doi: 10.1038/s41598-025-30803-x

    Figure Lengend Snippet: MCF7 and T47D seeded in Matrigel matrix and treated with the free combination, and HG-Combination at 72 h ( n = 3). The diameter of 3D structures was quantified (µm). All three replicates for each sample are represented as mean ± standard error of the mean (SEM). * p < 0.05;** p < 0.01; *** p < 0.001.

    Article Snippet: Luminal breast cancer cell lines MCF7 and T47D, non-tumorigenic keratinocyte cell line HaCaT, and non-tumoral breast epithelial cell line MCF10A were purchased from ATCC (Manassas, VA, USA).

    Techniques:

    Effect of HG-Combination on cell cycle and cell death by flow cytometry of MCF7 and T47D cancer cell lines. Empty hydrogel (HG) were used as control. ( A ) Assessment of the influence of treatment (0.5 µM ARV-471 and 5 µM Palbociclib, for 24 h) on cell cycle phases ( n = 3). All three replicates for each sample are represented as mean ± standard error of the mean (SEM). T-test analysis was performed to compare percentage of G0/G1 phase between each treatment and control (non-treated) cells. * p < 0.05; ** p < 0.01; *** p < 0.001. ( B ) Assessment of treatment (0.5 µM ARV-471 and 5 µM Palbociclib, for 72 h) on the cell death of MCF7 and T47D. Cells were classified into different populations: early apoptotic (AV-positive, PI-negative), late apoptotic (AV-positive and PI-positive) and necrotic (annexin V-negative, PI-positive). All three replicates for each sample are represented as mean ± standard error of the mean (SEM). T-test analysis was performed to compare percentage of AV-positive between each treatment and control (non-treated) cells. * p < 0.05; ** p < 0.01; *** p < 0.001.

    Journal: Scientific Reports

    Article Title: Dual-drug codelivery gelatin-based hydrogel of ARV-471 and Palbociclib enhances synergistic effect in breast cancer treatment

    doi: 10.1038/s41598-025-30803-x

    Figure Lengend Snippet: Effect of HG-Combination on cell cycle and cell death by flow cytometry of MCF7 and T47D cancer cell lines. Empty hydrogel (HG) were used as control. ( A ) Assessment of the influence of treatment (0.5 µM ARV-471 and 5 µM Palbociclib, for 24 h) on cell cycle phases ( n = 3). All three replicates for each sample are represented as mean ± standard error of the mean (SEM). T-test analysis was performed to compare percentage of G0/G1 phase between each treatment and control (non-treated) cells. * p < 0.05; ** p < 0.01; *** p < 0.001. ( B ) Assessment of treatment (0.5 µM ARV-471 and 5 µM Palbociclib, for 72 h) on the cell death of MCF7 and T47D. Cells were classified into different populations: early apoptotic (AV-positive, PI-negative), late apoptotic (AV-positive and PI-positive) and necrotic (annexin V-negative, PI-positive). All three replicates for each sample are represented as mean ± standard error of the mean (SEM). T-test analysis was performed to compare percentage of AV-positive between each treatment and control (non-treated) cells. * p < 0.05; ** p < 0.01; *** p < 0.001.

    Article Snippet: Luminal breast cancer cell lines MCF7 and T47D, non-tumorigenic keratinocyte cell line HaCaT, and non-tumoral breast epithelial cell line MCF10A were purchased from ATCC (Manassas, VA, USA).

    Techniques: Flow Cytometry, Control