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Ht 29

Manufactured by Avantor
Sourced in Denmark

HT-29 is a human colon adenocarcinoma cell line. It is a commonly used in vitro model for colorectal cancer research.

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2 protocols using ht 29

1

Cell line cultivation protocols

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Two non–small cell lung adenocarcinoma (NSCLC) cell lines NCI‐H2228 and NCI‐H1975, and two colon and CRC adenocarcinoma cell lines HT‐29 and KM12 were used in this study. NCI‐H2228 (non–small cell lung adenocarcinoma), NCI‐H1975 (non–small cell lung adenocarcinoma), and HT‐29 (colorectal adenocarcinoma) cell lines were acquired from American Type Culture Collection (ATCC, Manassas, VA). KM12 (colon adenocarcinoma) cell line was acquired from the NCI‐Fredrick Cancer DCTD Tumor/Cell line Repository (NCI, Frederick, MD). Media (Roswell Park Memorial Institute Medium 1640 for NCI‐H2228, NCI‐H1975, and KM12 cells, and McCoy's 5A Medium Modified for HT‐29 cells) were purchased from ATCC and supplemented with 1% penicillin‐streptomycin (HyClone GE Healthcare Life Sciences, Logan, UT). Media for NCI‐H2228, NCI‐H1975, and HT‐29 cells were supplemented with 10% Seradigm premium fetal bovine serum (VWR Life Science, Radnor, PA), and medium for KM12 cells were supplemented with 20% fetal bovine serum (Seradigm). Cells were cultured in 3D culture systems (see Section 2.2) and maintained according to manufacturers’ specifications. All cell lines were certified mycoplasma free.
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2

Xenograft Tumor Models of Colorectal and Lung Cancers

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All animal experiments were approved by the Danish Animal Welfare Council, Ministry of Justice. Upon arrival, Naval Medical Research Institute (NMRI) nude mice (Taconic Europe, Lille Skensved, Denmark) were acclimatized for one week in the animal facility and had at all times access to water and chow ad libitum. Human colorectal cancer cells, HT29 (n = 2), (American Type Culture Collection, Manassas, VA, USA), and human neuroendocrine lung cancer cells, H727 (n = 2) (The European Collection of Cell Cultures, Salisbury, UK) were cultured at 37 °C and 5% CO2 in McCoy’s 5A and RPMI-1640 Glutamax medium with 10% fetal calf serum and 1% penicillin-streptomycin, respectively (all Invitrogen Ltd., Paisley, UK). Mice were inoculated with approximately 106 of either HT29 or H727 cells, suspended in 200 μL (1:1 cell culture medium and BD™ Matrigel™ (VWR, Søborg, Denmark)), into each flank. Tumors were allowed to grow 2–3 weeks.
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