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2 protocols using csc medium

1

Propagation and Maintenance of Cancer Cell Lines

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Human lung epithelial adenocarcinoma cells (NCI-H23; CRL-10317TM, ATCC, University Boulevard, Manassas VA, USA) were cultured in RPMI 1640 supplemented with 10% heat-inactivated fetal bovine serum (FBS; ATCC), 1% antibiotic- antimycotic (anti-anti, Gibco, Grand Island, NY, USA), MEM non-essential amino acids (Gibco, Grand Island, NY, USA) and sodium pyruvate (Gibco, Grand Island, NY, USA). Human breast epithelial cells (MCF 10A; ATCC, University Boulevard, Manassas VA, USA) were cultured in DMEM/F12 medium (Invitrogen, Carlsbad, CA, USA (supplemented with 5% horse serum ((Invitrogen) along with 20 ng/mL EGF (Sigma-Aldrich, St. Louis, MO, USA), 1% hydrocortisone (Sigma-Aldrich), 100 ng/mL cholera toxin (Sigma-Aldrich), 0.02% insulin (Sigma-Aldrich) and 1% antibiotic- antimycotic. CSCs were prepared from NCI-H23 cells by culture the cells on 6 well ultralow cell adhesion plate with CSC medium (PromoCell, Sickingenstr, Heidelberg, Germany) according to the manufacturer's instruction. CSC tumor spheres were collected after 9 days of culture. All cells were maintained under humidified atmosphere of 5% CO2 at 37°C.
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2

Spheroid Formation Assay for CRC Cells

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To investigate the capacity of CRC cells to grow under non-adherent conditions, cells were seeded at a density of 1.5 × 106 cells in 10 cm plates. After 24 h of recovery, the cells were treated with increasing concentrations of SARB (10, 20, 50 μM) or Combi 35 µM. Incubation continued for another 48 h, then the cells were washed with PBS, trypsinized and 5 × 104 cells were then seeded in ultra-low attachment (ULA) six-well plates (Corning) in 2 ml of CSC medium (PromoCell) and 40 μl Matrigel with growth factors (Corning). Spheroid formation was monitored 7 days after seeding and then the spheroids were transferred to 15 ml falcon tubes, washed with PBS, trypsinzed, and 2.5 × 104 cells were seeded in ULA six-well plates with 2 ml CSC medium and 40 μl Matrigel. Cells were let grow for another 14 days and fresh medium was added every 2–3 days. At day 21, the spheroid growth was documented by light microscopy using a Nikon Eclipse Ti–S microscope or Leica DMI1 light microscope. The images were then analyzed using a macro (given in SI) which was imported to ImageJ (modified from ref. 58 (link)) to determine spheroid number.
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