Androgen-positive LNCaP, VCaP, C4-2B and 22RV1, and androgen-negative PC3 and DU145 cells were amplified and frozen upon receipt. LNCaP, 22RV1, DU145 and PC3 cell lines were cultured in RPMI1640 culture medium supplemented with 10% fetal bovine serum and 1% of Penicillin/Streptomycin 5000 U/mL. VCaP cells were cultured in DMEM culture medium supplemented with 10% fetal bovine serum and 1% of Penicillin/Streptomycin 5000 U/mL. C4-2B cells were cultured in DMEM/F12 (4:1, v/v) culture medium supplemented with 10% fetal bovine serum, 0.1 μg/mL insulin, 275 ng/mL triiodothyronine, 88.6 ng/mL apo-transferrin, 4.9 ng/mL d-Biotin, 252 ng/mL adenine and 1% of Penicillin/Streptomycin 5000 U/mL. Cells were cultured in a humidified incubator at 37°C with 5% CO2 and were routinely tested negative to Mycoplasma contamination using the MycoAlert Mycoplasma Detection kit. All commercially obtained cells were authenticated by the vendors. All compounds were dissolved in DMSO.
Do you have any questions about this protocol?
Post your question to gather feedback from the community. We will also invite the authors of this article to respond.