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Hydrocortisone

Manufactured by Santa Cruz Biotechnology
Sourced in United States

Hydrocortisone is a laboratory reagent used in scientific research. It is a synthetic glucocorticoid hormone that mimics the effects of the natural hormone cortisol. Hydrocortisone is commonly used in cellular and biochemical studies to investigate the role of glucocorticoid signaling pathways.

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3 protocols using hydrocortisone

1

Cell Culture Maintenance Protocols

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All the cells used in this study were all purchased from the American Type Culture Collection. MDA-MB-436 (Mb436) cells were maintained in L15 (HyClone, USA) supplemented with 10% fetal bovine serum (FBS) (Gibco, USA). SUM159 cells were maintained in Ham's F12 medium (Invitrogen, USA) supplemented with 5% FBS, 5 μg/mL insulin, and 1 μg/mL hydrocortisone (Santa Cruz, USA). MDA-MB-231 (Mb231),MDA-MB-453(Mb453) and Hs578T cells were maintained in DMEM containing 10% fetal bovine serum (FBS). All cells were cultured at 37°C in 5% CO2 and 100% humidity.
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2

Breast Cancer Cell Line Responses to Guadecitabine and IFNy

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Human breast cancer cell lines MCF7, BT474, BT549, and HCC1395 were obtained from ATCC. MCF7 and BT474 were grown in DMEM (Gibco) supplemented with 10% fetal bovine serum (FBS) (Denville). BT549 and HCC1395 were grown in RPMI (Gibco) supplemented with 10% FBS. The murine mammary carcinoma cell line, MMTV-Neu, was originally isolated from a primary mammary tumor (transgenic FVB/N mice) and cultured in DMEM/F12 (Gibco) supplemented with 10% FBS, 20 ng/ml EGF (Gibco), 0.5 µg/ml Hydrocortisone (Santa Cruz), and 10 µg/ml Insulin (Gibco). MCF7, BT474, BT549, HCC1395, and MMTV-Neu cells were pre-treated with diluent (Astex Pharmaceuticals), 0.05 µg/ml guadecitabine (Astex Pharmaceuticals) or 0.5 µg/ml guadecitabine for 3 days and stimulated with 100 ng/ml IFNγ (Gibco) for an additional 3 days with or without the presence of diluent control or guadecitabine. All cell lines were routinely tested for mycoplasm contamination.
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Cell Culture Conditions for Various Cell Lines

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HGE-20 cells [50 (link)] were grown in 50:50 DMEM:F12 (DMEM-Cellgro Mediatech, Manassas, VA, USA, F12-Life Technologies, Carlsbad, CA, USA) with 10% FBS (Gemini Bio-Products, West Sacremento, CA, USA) and 100 units/ml penicillin, 0.1 mg/ml streptomycin (Sigma, St. Louis, MO, USA). HGE-20 cells were provided by Dr. Daniel Mènard, who kindly granted permission to use the cells for this work. AGS, HEK-293, A549 and MDCK cells (ATCC, Manassas, VA, USA) and HGT-1 cells [51 (link)] were grown in DMEM medium (Cellgro Mediatech) containing 4.5 g/L glucose, 2 mM L-glutamine, 8 mg/L phenol red, 100 units/ml penicillin, 0.1 mg/ml streptomycin, and 10% FBS. The growth media for A549 cells was supplemented with 20 mM HEPES. PC12 cells (ATCC) were grown in RPMI 1640 with 2 mM GlutaMAX, 10 mM HEPES, 1 mM sodium pyruvate, 100 U/ml penicillin, and 100 μg/ml streptomycin (Sigma) supplemented with 10% FetalPlex animal serum complex (Gemini Bio-Products). Human mammary epithelial (HB2) cells [52 (link)] were maintained in DMEM supplemented with 10% FBS, 5 μg/ml hydrocortisone and 10 μg/ml insulin (Santa Cruz Biotechnology, Dallas, TX, USA). Human gastric antrum tissue was obtained through the UCLA TPCL program with a non-human subjects IRB exemption.
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