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5 protocols using mda mb 231

1

MDA-MB-231 Cell Culture Protocol

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The human TNBC cell line MDA-MB-231 (estrogen receptor negative, progesterone receptor negative, and human epidermal growth factor receptor-2 negative) was obtained from iCell Bioscience Inc. (Shanghai, China) and grown in Dulbecco’s Modified Eagle’s Medium (Invitrogen, Carlsbad, CA, USA) supplemented with 10% fetal bovine serum (FBS, Gibco, Gaithersburg, MD, USA) and 1% penicillin/streptomycin (Gibco). All cells were grown as monolayers and maintained in a cell culture incubator at 37°C and 5% CO2.
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2

Culturing Breast Cell Lines for Research

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Human normal breast MCF-10A cells (Zhongqiaoxinzhou Biotech, Shanghai China) were cultured in Mammary Epithelial Cell Medium (MEpiCm, ScienCell, Research Laboratoried, Carlsbad, CA, USA). BC cell lines, MDA-MB-231, MDA-MB-468, HCC-1937, MCF-7 (Chinese Academy of Science, Shanghai, China) and SKBR-3 (iCell Bioscience Inc, Shanghai, China) were cultured in Dulbecco's modi ed Eagle's medium (DMEM) (Gibco, Grand Island, NY, USA) with 10% Fetal Bovine Serum (FBS) (Gibco), penicillin (100 U/ml) and streptomycin (100 µg/ml) (PS, Enpromise, Hangzhou, China). Cells were incubated at 37 C supplemented with 5% CO 2 , and subcultured when the cell density was around 80%.
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3

Culturing Breast Cancer Cell Lines

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The MDA-MB-231, MDA-MB-453 and MDA-MB-468 human BC cell lines were incubated in L15 medium (LA9510; Beijing Solarbio Science & Technology Co., Ltd.) containing 10% FBS (SH30084.03; HyClone; Cytiva), 1% penicillin (C8251; Beijing Solarbio Science & Technology Co., Ltd.) and 1% streptomycin (S8290; Beijing Solarbio Science & Technology Co., Ltd.) in a 37°C, 5% CO2 incubator. The MCF-7 and ZR-75-1 cells were cultured with Minimum Essential Medium (MEM; 41500; Beijing Solarbio Science & Technology Co., Ltd.) containing 10% FBS, 1% penicillin (C8251; Beijing Solarbio Science & Technology Co., Ltd.) and 1% streptomycin (S8290; Beijing Solarbio Science & Technology Co., Ltd.) and RPMI-1640 (31800; Beijing Solarbio Science & Technology Co., Ltd.) medium containing 10% FBS, 1% penicillin (C8251; Beijing Solarbio Science & Technology Co., Ltd.) and 1% streptomycin (S8290; Beijing Solarbio Science & Technology Co., Ltd.) in a 37°C, 5% CO2 incubator, respectively. The MCF-10A cells were cultured in Mammary Epithelium Basal Medium (CC-3150; iCell Bioscience, Inc.) in a 37°C, 5% CO2 incubator. The MDA-MB-231, MDA-MB-453, MDA-MB-468, MCF-7 and MCF-10A cells were purchased from iCell Bioscience, Inc. The ZR-75-1 cells were purchased from Procell Life Science & Technology Co., Ltd.
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Cancer Cell Line Culturing Protocol

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Human breast cancer (MCF-7, MDA-MB-231),
urinary bladder cancer (T24), lung cancer (NCl-H1975), and monocytic
(Jurkat) cells were obtained from iCell (China). All cells were cultured
as recommended using phenol-red free Dulbecco’s Modified Eagle’s
Medium (DMEM) (Gibco, NY, USA) supplemented with 1% l-glutamine
(Life Technologies, CA, USA), 10% fetal bovine serum (FBS, Gibco),
and 1% penicillin/streptomycin (Corning, VA, USA), with the exception
of MCF-7, which were grown in 50:50 phenol-red free DMEM:F12 (Gibco)
supplemented with 1X B27 (Gibco), 5 mg/L insulin (MBL International
Corp., MA, USA), 20 μg/L basic fibroblast growth factor (bFGF,
Shenandoah Inc., PA, USA), 20 μg/L epidermal growth factor (EGF,
Shenandoah Inc., PA, USA), 1% penicillin/streptomycin (Corning, VA,
USA), 0.5 mg/L hydrocortisone (Sigma Aldrich, MO, USA), and 2.5 mM l-glutamine (Life Technologies, USA).
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5

Culturing Breast Cancer Cell Lines

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Human breast cancer cell lines MCF-7, MDA-MB-231, and MDA-MB-468 and normal mammary epithelial cell line MCF-10A were purchased from iCell Bioscience (Shanghai). Among them, MCF-7, MDA-MB-231, and MDA-MB-468 cells were cultured with the medium containing 90% RPMI 1640 and 10% fetal bovine serum (FBS). MCF-10A was cultured in DMEM/HAM F12 medium. All cell lines were cultured in a 5% CO2 cell incubator at 37°C and screened by qRT-PCR.
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