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2 protocols using skbr3 breast cancer cells

1

Culturing Breast and Prostate Cancer Cell Lines

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The SKBR3 breast cancer cells, obtained from ATCC, were maintained in DMEM (Sigma-Aldrich) with phenol red, supplemented with 10% fetal bovine serum (FBS), 1% penicillin/streptomycin and 1% Glutamax (Life Technologies). Human umbilical vein endothelial cells (HUVECs) were obtained from Sigma-Aldrich Co Limited and cultured in endothelial growth medium (EGM) (Lonza, Basel, Switzerland), supplemented with 5% FBS (Lonza). MCF7 breast and LnCAP prostate cancer cells, both obtained from American Type Culture Collection (ATCC, Manassas, VA, USA), were grown in DMEM and RPMI-1640 respectively, supplemented with 10% FBS, 1% penicillin/streptomycin and 1% Glutamax (Life Technologies). All cell lines were grown in a 37 ° C incubator with 5% CO2. Cells were switched to medium without serum the day before experiments.
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2

Cell Culture Protocols for Cancer Research

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SKOV-3 ovarian cancer cells, TiB-73 normal liver cells, HepG2 liver cancer cells, HCT-116 colon cancer cells, MDA-MB-231 breast cancer cells, SKBR3 breast cancer cells, and NCI-Adr-Res drug resistant ovarian cancer cells were purchased from ATCC. Cells were cultured at 37 °C under 5% CO2 in phenol red-containing Dulbecco’s modified Eagle medium (DMEM; Gibco Life Tech., cat. #11960-044) supplemented with 10% heat-inactivated fetal bovine serum (Omega scientific, cat. #FB02) and the antibiotics penicillin/streptomycin (Corning Cellgro, cat. #30-002-C1). Cells were sub-cultured in T-75 flasks at 70–80% confluency every 2–3 days.
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