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Prostate Cancer Cell Line Culture

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Human normal prostate stromal immortalized cell line WPMY-1 (BNCC100291) and PCa cell lines PC-3 (BNCC337715), Du 145 (BNCC338240), LNCaP (BNCC337703), and 22RV1 (BNCC100161) were bought from BeNa Culture Collection (Shanghai, China). Cells were prepared at 37℃ with 5% CO2. Culture medium information was: PC-3, Du 145, WPMY-1 cell lines in DMEM-H (BNCC338068) plus 10% FBS; LNCaP, 22RV1 cell lines in RPMI-1640 plus 10% FBS (BNCC341471). Du 145 cells were passaged in DMEM (Sigma-Aldrich) plus 10% dialyzed FBS (Gemini Bio-Products) in the methionine dependence assay. Control medium was supplemented with 100 µM l-methionine (Sigma-Aldrich), 100 µM l-cysteine (Fisher Scientific), 1.5 µM vitamin B12, and 4 mM l-glutamine. Also, 200 µM dl-homocysteine (Sigma-Aldrich) was added to the Met-Hcy+ medium. For sulfasalazine treatment, sulfasalazine (HY-14655, medchemexpress, USA) was purchased and dissolved in DMSO, and was added to the culture medium at a final concentration of 200 µM for treating PCa cells. The same amount of DMSO was supplemented to the control group for treatment [33 (link)].
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Prostate Cancer Cell Line Cultivation

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Human normal prostate epithelial cell line (WPMY-1) and two PCa cell lines (LNCaP-AI and DU145) were obtained from Bena Culture Collection (Beijing, China). Dulbecco’s Modified Eagle medium (DMEM; Gibco, Carlsbad, CA, USA) and Roswell Park Memorial Institute-1640 (RPMI-1640) medium (Gibco) were used for the cultivation of WPMY-1 and PCa cell lines, respectively. The base medium was supplemented with 10% fetal bovine serum (FBS; Biowest, Loire Valley, France) and 10% penicillin (100 U/mL)/streptomycin (100 μg/mL) mixture before use. Cell culture plates were maintained in a humidified 37°C incubator with 5% CO2.
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