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The SGC-7901 is a cell line derived from human gastric adenocarcinoma. It is a commonly used in vitro model for the study of gastric cancer biology and development of therapeutic interventions.

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342 protocols using sgc 7901

1

Gastric Cancer Cell Culture and Transfection

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Human gastric cancer BGC823 and SGC7901 cells were purchased from ATCC (Manassas, VA, USA) and cultured in RPMI-1640 (Gibco, Life Technologies, NY, USA) supplemented with 10% fetal bovine serum (FBS, ExCell Bio, Shanghai, China), 100 U/ml penicillin and 100 µg/mL streptomycin (Gibco). Plasmid DNA transfection was performed with Turbofect reagent (Invitrogen, CA, USA) according to the manufacturer’s instructions. 5-FU was purchased from Sigma and was added to subconfluent cells at the indicated doses.
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2

Gastric Cancer Cell Response to Deoxycholic Acid

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The human normal gastric epithelial cell line GES-1 and the human gastric cancer cell lines AGS, AZ-521, BGC823, SGC7901 and MKN45 (purchased from ATCC Manassas, US) were cultured in RPMI-1640 medium (Gibco, CA, US) supplemented with 10% fetal bovine serum (Biological Industries, Beit Haemek, Israel), 100 mg/ml streptomycin and 100 U/ml penicillin. All cells were incubated at 37 °C in a humidified incubator containing 5% CO2. Deoxycholic acid (DCA) (MedChem Express, US) was dissolved in dimethyl sulfoxide (DMSO). After 24 h of starvation, the cells were exposed to 50–200 µM DCA for 24 h. These doses of DCA were chosen from previous in vivo and in vitro studies [24 (link), 25 (link)].
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3

Cell Line Culture Protocols

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The PANC-1, HepG2, SGC-7901, and MDA-MB-231 cell lines were purchased from ATCC. The Panc02 cell line was acquired from Tong Pai Technology (Shanghai, China). PANC-1, HepG2, and MDA-MB-231 cell lines were cultured in DMEM (Thermo Fisher Scientific, USA) supplemented with 10% FBS (HyClone, USA) at 37 °C in a 5% CO2 incubator. SGC-7901 cells were cultured in RPMI 1640 containing 10% FBS under similar conditions.
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Comprehensive Gastric Cancer Cell Line Protocol

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The GES‐1 cell line was provided by the Shanghai Institute of Cell Biology, Chinese Academy of Sciences. The AGS, SGC‐7901, and SK‐GT5 cell lines were purchased from ATCC. SGC‐7901 and SK‐GT5 cells were cultivated in Dulbecco's modified Eagle's medium (DMEM) and an environment of 5% CO2 at 37°C, and GES‐1 cells were cultivated in Roswell Park Memorial Institute 1640 (RPMI 1640) medium supplemented with 10% fetal bovine serum (Life Technologies/Gibco), 100 U/mL penicillin, and 100 µg/mL streptomycin (Life Technologies/Gibco). The plasmids of αSR and CagA‐wild type were purchased from Dr Masanori Hatakeyama of Japan's Tokyo University. The pEGFP‐N1 plasmid was purchased from Clontech, the plasmids TET1‐wt and pX459 were obtained from Addgene, and pX459‐TET1‐sgRNA was constructed in the laboratory. The liposome transfection reagent Lipofectamine 3000 was purchased from Invitrogen in the United States. Antibodies against HA were purchased from OriGene, antibodies against CagA were purchased from Santa Cruz, antibodies against 5‐hmC were purchased from Active Motif, and antibodies against KLF4 and TET1 were purchased from Santa Cruz.
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5

Culturing Gastric Cancer Cell Lines

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Human gastric cancer cell lines including AGS, BGC-823, SGC-7901, and MGC-803, and normal human gastric mucosa epithelial cell line GES-1 were purchased from ATCC, USA. Cells were cultured in DMEM (Thermo Fisher, USA) supplemented with 10% fetal bovine serum (FBS, Thermo Fisher) in a 37°C humidified atmosphere of 5% CO2.
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6

Gastric Cancer Cell Line Culture

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Gastric cancer cell lines (SGC-7901, MKN-45, AGS, MKN-28, and MGC-803) and human normal gastric mucosal epithelial cells (NGEC) were purchased from ATCC (American Type Culture Collection, ATCC). NGEC, AGS cells were cultured in 90% DMEM (Biological Industries, Cat. No. 06-1055-57-1A), 10% FBS (Biological Industries, Cat. No. 04-007-1A), and 1% penicillin/streptomycin. SGC-7901, MKN-45, MKN-28, and MGC-803 cells were cultured in 90% RPMI (Biological Industries, Cat. No. 01-101-1A), 10% FBS, and 1% penicillin/streptomycin. Although MGC-803 cell reports show cross-contamination with HeLa, there are still many research groups using MGC-803 as a model for studying gastric cancer cells (Zhai et al., 2019 (link); Li et al., 2020 (link); Peng et al., 2020 (link)).
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Gastric Cell Line Culturing Protocol

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The human GC cell lines SGC-7901, MKN-28 and BGC-823 (ATCC, Manassas, VA, USA) and the human normal gastric epithelial cell line GES-1 (Shanghai Institute for Life Science, Chinese Academy of Sciences, Shanghai, China) were cultured in RPMI 1640 (Solarbio, Beijing, China) supplemented with 10% fetal bovine serum (Biological industries, USA) and incubated at 37 °C, 5% CO2, and saturated humidity.
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8

Gastric Cell Lines Culture Protocol

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We applied the normal human stomach epithelial cell line GES-1 (CBTCCCAS, Shanghai, China) and the human gastric adenocarcinoma cell lines AGS, SGC7901, BGC803, and BGC823 (ATCC, Manassas, VA, USA) in this study, and these cell lines were cultured in DMEM and RPMI-1640 (Invitrogen, Carlsbad, CA, USA), respectively at 37 °C in a humidified atmosphere with 5% CO2, which was supplemented with 10% fetal bovine serum (Hyclone, Logan, UT, USA), penicillin/streptomycin (1:100 dilution; Invitrogen), and 4 mM glutamine (Life Technologies, Gibco BRL).
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9

Cell Lines for Gastric Cancer Research

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GES-1 is a SV40 transformed human fetal gastric epithelial cell line, which were established in 1994 and proved to maintain a normal cytoskeleton, positive in PAS reaction and were non-tumourigenic in nude mice.30 (link) GES-1, SGC7901, MKN28, MKN45 and AGS cells (originally purchased from ATCC) were maintained in RPMI-1640 medium; BGC823 and HEK293T cells (originally purchased from ATCC) were cultured in Dulbecco’s modified Eagle’s medium (Thermo Scientific HyClone, Beijing, China).
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10

Gastric Cancer Cell Culture Protocol

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The GC lines MKN74, SGC7901, BGC823, MGC803, HGC27, and AGS and normal human gastric epithelial cell line GES1 were purchased from ATCC. SGC7901, BGC823, MGC803, HGC27, AGS, and GES1 were cultured in DMEM containing 10% FBS (HyClone Laboratories), 100 U/mL penicillin (Amresco), and 100 mg/mL streptomycin (Amresco). MKN74 cells were cultured in RPMI‐1640 (HyClone Laboratories) supplemented with 10% FBS, 100 U/mL penicillin, and 100 mg/mL streptomycin. All cells were incubated in a humidified atmosphere with CO2 at 37°C.
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