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bt549 breast cancer cell lines  (ATCC)


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    Structured Review

    ATCC bt549 breast cancer cell lines
    Bt549 Breast Cancer Cell Lines, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 3004 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/breast+cancer+cell+lines+bt549/BT-549/pm42092157-225-10-32
    Average 99 stars, based on 3004 article reviews
    bt549 breast cancer cell lines - by Bioz Stars, 2026-11
    99/100 stars

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    Related Articles

    Multiple Displacement Amplification:

    Article Title: Isoliquiritigenin Impedes Breast Cancer Progression through PITX1–PFKP-Mediated Glycolysis Reprogramming
    Article Snippet: .. All cell lines used in this research, including the normal mammary cell line MCF-10A and the breast cancer cell lines BT549, MDA-MB-231, SKBR3, BT474, MCF-7, and T47D, were commercially purchased from the ATCC (American Type Culture Collection; Manassas, VA, USA). .. All cell lines were maintained and cultured following the guidance and instructions of the ATCC library.

    Article Title: C1ql4 regulates breast cancer cell stemness and epithelial-mesenchymal transition through PI3K/AKT/NF-κB signaling pathway.
    Article Snippet: The antibodies were used as follows: C1ql4, b-actin (1:100 dilution, CST, USA). .. Breast cancer cell lines BT549, MDA-MB-231, MCF-7, and HCC1428 were bought from American Type Culture Collection (ATCC) and cultured in DMEM (Gibco, USA) with 10% fetal bovine serum (FBS; Gibco, USA) and 1% streptomycin/penicillin (Gibco, USA) in a humidified 37°C incubator that contains 5% CO2. ..

    Article Title: C1ql4 regulates breast cancer cell stemness and epithelial-mesenchymal transition through PI3K/AKT/NF-κB signaling pathway
    Article Snippet: The antibodies were used as follows: C1ql4, β-actin (1:100 dilution, CST, USA). .. Breast cancer cell lines BT549, MDA-MB-231, MCF-7, and HCC1428 were bought from American Type Culture Collection (ATCC) and cultured in DMEM (Gibco, USA) with 10% fetal bovine serum (FBS; Gibco, USA) and 1% streptomycin/penicillin (Gibco, USA) in a humidified 37°C incubator that contains 5% CO 2 . ..

    Article Title: MEK1 Inhibitor Combined with Irradiation Reduces Migration of Breast Cancer Cells Including miR-221 and ZEB1 EMT Marker Expression.
    Article Snippet: .. Growth and Maintenance of Cell Lines and 3D-Microtissue Generation The breast cancer cell lines BT549, HCC1806, MDA-MB-231, MDA-MB-468, MCF7, MDA-MB-361, SKBR3, and T47D (acquired from ATCC, Gaithersburg, MA, USA or DSMZ GmbH, Braunschweig, Germany collections) were maintained in DMEM (Dulbecco’s Modified Eagle Medium) supplemented with 10% FCS and non-essential amino acids (Sigma Aldrich, St. Lois, MO, USA) when necessary or in RPMI 1640 (Roswell Park Memorial Institute) medium supplemented with 10% FCS and human insulin (10 μg/mL). .. The human embryonic kidney HEK293T cells (from DSMZ GmbH collection) were used for lentivirus productions and grown in DMEM medium with 10% FCS.

    Article Title: Targeting CLK4 inhibits the metastasis and progression of breast cancer by inactivating TGF-β pathway.
    Article Snippet: Triple-negative breast cancer (TNBC) represents the most aggressive subtype of breast cancer that is highly resistant to current therapeutic options.. According to the public databases Oncomine and KM plotter, the CLK4 expression is correlated with poor patient survival in TNBC, especially in mesenchymal-like TNBC (MES-TNBC) that has strong metastatic potential.. Therefore, we investigated the potential involvement of CLK4 in the metastasis and progression of MES-TNBC.

    Article Title: Functional screening reveals HORMAD1-driven gene dependencies associated with translesion synthesis and replication stress tolerance
    Article Snippet: .. The following breast cancer cell lines BT549, HCC38, HCC1143, MDA-MB-436; the immortalised mammary epithelial cell line MCF10A and the immortalised retinal pigment epithelial cell line RPE-1 were obtained from the American Type Culture Collection (ATCC, Manassas, VA, USA). .. The breast cancer cell line SUM159 was obtained from Asterand (Royston, UK).

    Article Title: MEK1 Inhibitor Combined with Irradiation Reduces Migration of Breast Cancer Cells Including miR-221 and ZEB1 EMT Marker Expression
    Article Snippet: .. The breast cancer cell lines BT549, HCC1806, MDA-MB-231, MDA-MB-468, MCF7, MDA-MB-361, SKBR3, and T47D (acquired from ATCC, Gaithersburg, MA, USA or DSMZ GmbH, Braunschweig, Germany collections) were maintained in DMEM (Dulbecco’s Modified Eagle Medium) supplemented with 10% FCS and non-essential amino acids (Sigma Aldrich, St. Lois, MO, USA) when necessary or in RPMI 1640 (Roswell Park Memorial Institute) medium supplemented with 10% FCS and human insulin (10 μg/mL). .. The human embryonic kidney HEK293T cells (from DSMZ GmbH collection) were used for lentivirus productions and grown in DMEM medium with 10% FCS.

    Article Title: Knockdown of XB130 restrains cancer stem cell-like phenotype through inhibition of Wnt/β-Catenin signaling in breast cancer.
    Article Snippet: .. A nontumorigenic epithelial cell line MCF‐10a, and breast cancer cell lines BT549, MCF‐7, MDA‐MB‐468, MDA‐MB‐231, T47D, ZR‐75‐30, and HCC1954 were purchased from ATCC. .. The MCF‐10a cells were maintained in mammary epithelial cell growth medium (MEGM) bullet Kit (Lonza, Basel, CHE), and seven breast cancer cell lines were cultured in Dulbecco’s modified Eagle’s medium (DMEM) medium (Gibco, Grand Island, NY) according to the ATCC protocol.

    Cell Culture:

    Article Title: C1ql4 regulates breast cancer cell stemness and epithelial-mesenchymal transition through PI3K/AKT/NF-κB signaling pathway.
    Article Snippet: The antibodies were used as follows: C1ql4, b-actin (1:100 dilution, CST, USA). .. Breast cancer cell lines BT549, MDA-MB-231, MCF-7, and HCC1428 were bought from American Type Culture Collection (ATCC) and cultured in DMEM (Gibco, USA) with 10% fetal bovine serum (FBS; Gibco, USA) and 1% streptomycin/penicillin (Gibco, USA) in a humidified 37°C incubator that contains 5% CO2. ..

    Article Title: C1ql4 regulates breast cancer cell stemness and epithelial-mesenchymal transition through PI3K/AKT/NF-κB signaling pathway
    Article Snippet: The antibodies were used as follows: C1ql4, β-actin (1:100 dilution, CST, USA). .. Breast cancer cell lines BT549, MDA-MB-231, MCF-7, and HCC1428 were bought from American Type Culture Collection (ATCC) and cultured in DMEM (Gibco, USA) with 10% fetal bovine serum (FBS; Gibco, USA) and 1% streptomycin/penicillin (Gibco, USA) in a humidified 37°C incubator that contains 5% CO 2 . ..

    Article Title: Targeting CLK4 inhibits the metastasis and progression of breast cancer by inactivating TGF-β pathway.
    Article Snippet: Triple-negative breast cancer (TNBC) represents the most aggressive subtype of breast cancer that is highly resistant to current therapeutic options.. According to the public databases Oncomine and KM plotter, the CLK4 expression is correlated with poor patient survival in TNBC, especially in mesenchymal-like TNBC (MES-TNBC) that has strong metastatic potential.. Therefore, we investigated the potential involvement of CLK4 in the metastasis and progression of MES-TNBC.

    Modification:

    Article Title: MEK1 Inhibitor Combined with Irradiation Reduces Migration of Breast Cancer Cells Including miR-221 and ZEB1 EMT Marker Expression.
    Article Snippet: .. Growth and Maintenance of Cell Lines and 3D-Microtissue Generation The breast cancer cell lines BT549, HCC1806, MDA-MB-231, MDA-MB-468, MCF7, MDA-MB-361, SKBR3, and T47D (acquired from ATCC, Gaithersburg, MA, USA or DSMZ GmbH, Braunschweig, Germany collections) were maintained in DMEM (Dulbecco’s Modified Eagle Medium) supplemented with 10% FCS and non-essential amino acids (Sigma Aldrich, St. Lois, MO, USA) when necessary or in RPMI 1640 (Roswell Park Memorial Institute) medium supplemented with 10% FCS and human insulin (10 μg/mL). .. The human embryonic kidney HEK293T cells (from DSMZ GmbH collection) were used for lentivirus productions and grown in DMEM medium with 10% FCS.

    Article Title: MEK1 Inhibitor Combined with Irradiation Reduces Migration of Breast Cancer Cells Including miR-221 and ZEB1 EMT Marker Expression
    Article Snippet: .. The breast cancer cell lines BT549, HCC1806, MDA-MB-231, MDA-MB-468, MCF7, MDA-MB-361, SKBR3, and T47D (acquired from ATCC, Gaithersburg, MA, USA or DSMZ GmbH, Braunschweig, Germany collections) were maintained in DMEM (Dulbecco’s Modified Eagle Medium) supplemented with 10% FCS and non-essential amino acids (Sigma Aldrich, St. Lois, MO, USA) when necessary or in RPMI 1640 (Roswell Park Memorial Institute) medium supplemented with 10% FCS and human insulin (10 μg/mL). .. The human embryonic kidney HEK293T cells (from DSMZ GmbH collection) were used for lentivirus productions and grown in DMEM medium with 10% FCS.



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    PAK2 expression and cluster formation in breast cancer cell lines. a mRNA expression levels of PAK2 in breast cancer cell lines and the normal mammary epithelial cell line MCF10A. b – f Quantification of cell cluster formation in four breast cancer cell lines under suspension culture conditions at 12, 24, and 48 h. g Immunoblot analysis of total PAK2 and phospho-PAK2 (Ser141) levels in <t>BT549,</t> MDA-MB-231, SKBR3, and AU565 breast cancer cells. SKBR3 cells were used as the reference (set to 1) for relative expression
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    YH395A inhibited breast cancer cell proliferation. (A) Breast cancer cell lines (MDA-MB-231, MDA-MB-468, <t>BT549,</t> SUM159, and BT-20), normal mammary epithelial cells (MCF-10 A), human gastric mucosal epithelial cells (GES-1), and human embryonic lung fibroblast cells (MRC-5) were treated with the indicated concentrations of YH395A or YR-290. After 96 h, SRB assay was performed. The bars indicate the mean ± SD. (B) Colony formation assays of breast cancer cells
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    ATCC bt549 human breast cancer cell line
    YH395A inhibited breast cancer cell proliferation. (A) Breast cancer cell lines (MDA-MB-231, MDA-MB-468, <t>BT549,</t> SUM159, and BT-20), normal mammary epithelial cells (MCF-10 A), human gastric mucosal epithelial cells (GES-1), and human embryonic lung fibroblast cells (MRC-5) were treated with the indicated concentrations of YH395A or YR-290. After 96 h, SRB assay was performed. The bars indicate the mean ± SD. (B) Colony formation assays of breast cancer cells
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    Image Search Results


    PAK2 expression and cluster formation in breast cancer cell lines. a mRNA expression levels of PAK2 in breast cancer cell lines and the normal mammary epithelial cell line MCF10A. b – f Quantification of cell cluster formation in four breast cancer cell lines under suspension culture conditions at 12, 24, and 48 h. g Immunoblot analysis of total PAK2 and phospho-PAK2 (Ser141) levels in BT549, MDA-MB-231, SKBR3, and AU565 breast cancer cells. SKBR3 cells were used as the reference (set to 1) for relative expression

    Journal: Breast Cancer Research : BCR

    Article Title: PAK2 promotes CTC cluster formation by phosphorylating E-cadherin to enhance cell-cell adhesion in breast cancer

    doi: 10.1186/s13058-025-02199-z

    Figure Lengend Snippet: PAK2 expression and cluster formation in breast cancer cell lines. a mRNA expression levels of PAK2 in breast cancer cell lines and the normal mammary epithelial cell line MCF10A. b – f Quantification of cell cluster formation in four breast cancer cell lines under suspension culture conditions at 12, 24, and 48 h. g Immunoblot analysis of total PAK2 and phospho-PAK2 (Ser141) levels in BT549, MDA-MB-231, SKBR3, and AU565 breast cancer cells. SKBR3 cells were used as the reference (set to 1) for relative expression

    Article Snippet: The human breast cancer cell lines BT549, MDA-MB-231, SKBR3, AU565, along with the normal mammary epithelial cell line MCF10A, were purchased from the American Type Culture Library (ATCC, Manassas, Virginia, USA).

    Techniques: Expressing, Suspension, Western Blot

    PAK2 promotes cell cluster formation. a , b Immunoblot analysis showing PAK2 expression in BT549 cells after overexpression or knockdown. c Representative images and quantification of cluster formation in BT549 cells transfected with control vector (Con) or lenti-PAK2 (OE-PAK2). d Representative images and quantification of cluster formation in BT549 cells transfected with control siRNA (siCon) or siPAK2-1

    Journal: Breast Cancer Research : BCR

    Article Title: PAK2 promotes CTC cluster formation by phosphorylating E-cadherin to enhance cell-cell adhesion in breast cancer

    doi: 10.1186/s13058-025-02199-z

    Figure Lengend Snippet: PAK2 promotes cell cluster formation. a , b Immunoblot analysis showing PAK2 expression in BT549 cells after overexpression or knockdown. c Representative images and quantification of cluster formation in BT549 cells transfected with control vector (Con) or lenti-PAK2 (OE-PAK2). d Representative images and quantification of cluster formation in BT549 cells transfected with control siRNA (siCon) or siPAK2-1

    Article Snippet: The human breast cancer cell lines BT549, MDA-MB-231, SKBR3, AU565, along with the normal mammary epithelial cell line MCF10A, were purchased from the American Type Culture Library (ATCC, Manassas, Virginia, USA).

    Techniques: Western Blot, Expressing, Over Expression, Knockdown, Transfection, Control, Plasmid Preparation

    Effects of PAK2 on breast cancer cell progression. a , b Colony formation assays performed in BT549 cells with PAK2 overexpression or knockdown. c , d Wound healing assays evaluating the migration of BT549 cells with PAK2 overexpression or knockdown. e Transwell assays evaluating the invasive capacity of BT549 cells with PAK2 overexpression or knockdown

    Journal: Breast Cancer Research : BCR

    Article Title: PAK2 promotes CTC cluster formation by phosphorylating E-cadherin to enhance cell-cell adhesion in breast cancer

    doi: 10.1186/s13058-025-02199-z

    Figure Lengend Snippet: Effects of PAK2 on breast cancer cell progression. a , b Colony formation assays performed in BT549 cells with PAK2 overexpression or knockdown. c , d Wound healing assays evaluating the migration of BT549 cells with PAK2 overexpression or knockdown. e Transwell assays evaluating the invasive capacity of BT549 cells with PAK2 overexpression or knockdown

    Article Snippet: The human breast cancer cell lines BT549, MDA-MB-231, SKBR3, AU565, along with the normal mammary epithelial cell line MCF10A, were purchased from the American Type Culture Library (ATCC, Manassas, Virginia, USA).

    Techniques: Over Expression, Knockdown, Migration

    PAK2 mediates cell cluster formation via E-cadherin phosphorylation. a , b GSEA showing the association between PAK2 and the adherens junction pathway. c , d Immunoblot analysis of E-cadherin and phosphorylated E-cadherin (Ser840) in BT549 cells after PAK2 overexpression or knockdown

    Journal: Breast Cancer Research : BCR

    Article Title: PAK2 promotes CTC cluster formation by phosphorylating E-cadherin to enhance cell-cell adhesion in breast cancer

    doi: 10.1186/s13058-025-02199-z

    Figure Lengend Snippet: PAK2 mediates cell cluster formation via E-cadherin phosphorylation. a , b GSEA showing the association between PAK2 and the adherens junction pathway. c , d Immunoblot analysis of E-cadherin and phosphorylated E-cadherin (Ser840) in BT549 cells after PAK2 overexpression or knockdown

    Article Snippet: The human breast cancer cell lines BT549, MDA-MB-231, SKBR3, AU565, along with the normal mammary epithelial cell line MCF10A, were purchased from the American Type Culture Library (ATCC, Manassas, Virginia, USA).

    Techniques: Phospho-proteomics, Western Blot, Over Expression, Knockdown

    PAK2 interacts and colocalizes with E-cadherin. a Protein docking map and binding site of PAK2 for E-cadherin. The yellow color represents PAK2, and the blue color represents E-cadherin. b IF staining illustrating the colocalization of PAK2 and E-cadherin in MCF10A and BT549. c Co-IP analysis showing the association between PAK2 and E-cadherin in breast cancer cells

    Journal: Breast Cancer Research : BCR

    Article Title: PAK2 promotes CTC cluster formation by phosphorylating E-cadherin to enhance cell-cell adhesion in breast cancer

    doi: 10.1186/s13058-025-02199-z

    Figure Lengend Snippet: PAK2 interacts and colocalizes with E-cadherin. a Protein docking map and binding site of PAK2 for E-cadherin. The yellow color represents PAK2, and the blue color represents E-cadherin. b IF staining illustrating the colocalization of PAK2 and E-cadherin in MCF10A and BT549. c Co-IP analysis showing the association between PAK2 and E-cadherin in breast cancer cells

    Article Snippet: The human breast cancer cell lines BT549, MDA-MB-231, SKBR3, AU565, along with the normal mammary epithelial cell line MCF10A, were purchased from the American Type Culture Library (ATCC, Manassas, Virginia, USA).

    Techniques: Binding Assay, Staining, Co-Immunoprecipitation Assay

    FRAX597 inhibits PAK2 activity and CTC cluster formation. a CCK-8 assay evaluating the viability of BT549 after 48 h treatment with FRAX597. b Immunoblot analysis of total PAK2 and phosphorylated PAK2 protein levels in BT549 treated with 2.5 or 5 µM FRAX597 for 24 and 48 h. c Representative images and quantification of BT549 cell aggregation after 24 h FRAX597 treatment. d Immunoblot analysis of total and phosphorylated PAK2, and total and phosphorylated E-cadherin in BT549 treated with 2.5 or 5 µM FRAX597 for 24 h

    Journal: Breast Cancer Research : BCR

    Article Title: PAK2 promotes CTC cluster formation by phosphorylating E-cadherin to enhance cell-cell adhesion in breast cancer

    doi: 10.1186/s13058-025-02199-z

    Figure Lengend Snippet: FRAX597 inhibits PAK2 activity and CTC cluster formation. a CCK-8 assay evaluating the viability of BT549 after 48 h treatment with FRAX597. b Immunoblot analysis of total PAK2 and phosphorylated PAK2 protein levels in BT549 treated with 2.5 or 5 µM FRAX597 for 24 and 48 h. c Representative images and quantification of BT549 cell aggregation after 24 h FRAX597 treatment. d Immunoblot analysis of total and phosphorylated PAK2, and total and phosphorylated E-cadherin in BT549 treated with 2.5 or 5 µM FRAX597 for 24 h

    Article Snippet: The human breast cancer cell lines BT549, MDA-MB-231, SKBR3, AU565, along with the normal mammary epithelial cell line MCF10A, were purchased from the American Type Culture Library (ATCC, Manassas, Virginia, USA).

    Techniques: Activity Assay, CCK-8 Assay, Western Blot

    FRAX597 suppresses breast cancer progression. a – c Effects of FRAX597 on BT549 cell proliferation, migration and invasion. d Schematic diagram of in vivo experimental design. e , f Tumor volume, tumor weight and body weight measurements of nude mice treated with FRAX597

    Journal: Breast Cancer Research : BCR

    Article Title: PAK2 promotes CTC cluster formation by phosphorylating E-cadherin to enhance cell-cell adhesion in breast cancer

    doi: 10.1186/s13058-025-02199-z

    Figure Lengend Snippet: FRAX597 suppresses breast cancer progression. a – c Effects of FRAX597 on BT549 cell proliferation, migration and invasion. d Schematic diagram of in vivo experimental design. e , f Tumor volume, tumor weight and body weight measurements of nude mice treated with FRAX597

    Article Snippet: The human breast cancer cell lines BT549, MDA-MB-231, SKBR3, AU565, along with the normal mammary epithelial cell line MCF10A, were purchased from the American Type Culture Library (ATCC, Manassas, Virginia, USA).

    Techniques: Migration, In Vivo

    YH395A inhibited breast cancer cell proliferation. (A) Breast cancer cell lines (MDA-MB-231, MDA-MB-468, BT549, SUM159, and BT-20), normal mammary epithelial cells (MCF-10 A), human gastric mucosal epithelial cells (GES-1), and human embryonic lung fibroblast cells (MRC-5) were treated with the indicated concentrations of YH395A or YR-290. After 96 h, SRB assay was performed. The bars indicate the mean ± SD. (B) Colony formation assays of breast cancer cells

    Journal: Cell Communication and Signaling : CCS

    Article Title: Artificial intelligence-driven discovery of YH395A: A novel TGFβR1 inhibitor with potent anti-tumor activity against triple-negative breast cancer

    doi: 10.1186/s12964-025-02337-2

    Figure Lengend Snippet: YH395A inhibited breast cancer cell proliferation. (A) Breast cancer cell lines (MDA-MB-231, MDA-MB-468, BT549, SUM159, and BT-20), normal mammary epithelial cells (MCF-10 A), human gastric mucosal epithelial cells (GES-1), and human embryonic lung fibroblast cells (MRC-5) were treated with the indicated concentrations of YH395A or YR-290. After 96 h, SRB assay was performed. The bars indicate the mean ± SD. (B) Colony formation assays of breast cancer cells

    Article Snippet: The MCF-10 A, GES-1, MRC-5, and triple-negative breast cancer (TNBC) cell lines BT549 (RRID: CVCL_0062), MDA-MB-468 (RRID: CVCL_0419), BT-20 (RRID: CVCL_0169), and MDA-MB-231(RRID: CVCL_0063) were sourced from the American Type Culture Collection (ATCC, USA), while SUM159 cells were generously donated by Dr. Yuzhu Zhang (Guangdong Academy of Chinese Medicine, China).

    Techniques: Sulforhodamine B Assay