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Snu478

Manufactured by Korean Cell Line Bank
Sourced in Japan

The SNU478 is a cell culture incubator designed for maintaining optimal growth conditions for cell lines. It features precise temperature, humidity, and CO2 control to create a stable environment for cell culture applications.

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15 protocols using snu478

1

Cell Line Culturing and Authentication

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Human SNU-245 and SNU-478 cell lines were purchased from the Korean Cell Line Bank (Seoul, Korea) and authenticated prior to receipt. Early passage cells were cultured in RPMI-1640 media (Gibco, Gaithersburg, MD, USA) containing 10% foetal bovine serum (FBS), 10 mM L-glutamine, and Antibiotic-Antimycotic (Thermo Fisher Scientific). Human BTC cell lines HuCCT1, HuH28, and WITT were a gift from Dr. Tushar Patel (Mayo Clinic, Jacksonville, FL), and Mz-ChA-1 was a gift from Dr. Shannon Glaser (Texas A&M Health Sciences Center, Bryan, TX).39 (link) These cells were authenticated through ATCC cell line authentication service (Kit #135-XV). HuCCT1 and HuH28 cells were cultured in RPMI-1640 media (Gibco) containing 10% FBS, 10 mM L-glutamine, and antibiotics. Mz-ChA-1 cells were cultured in CMRL1-media (Gibco) containing 10% FBS, 10 mM L-glutamine, and antibiotics.
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2

Establishment of Gemcitabine-Resistant CCA Cell Lines

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CCA cell lines HuCCT1 and HuH28 were purchased from Japan Health Science Research Resources Bank, and CCA cell lines SNU-1196, SNU-1079, SNU-308, SNU-245, SNU-478 and SNU-869 were purchased from Korea Cell Line Bank. Human HEK293T was obtained from American Type Culture Collection (ATCC). All cell lines were cultured with RPMI-1640 medium (Invitrogen, USA) supplemented with 10% fetal bovine serum (Hyclone, USA) and 1% PenStrep (100 U/mL Penicilium and 100 μg/mL Streptomycin) in a humid atmosphere containing 5% CO2 at 37 °C. Gemcitabine resistant cell lines HuCCT1-Gem and SNU-245-Gem were constructed by exposing to increasing dosages of Gemcitabine (Selleck Chemicals, USA) for 8 months, and then persistently cultured in medium containing 10 nmol/l Gemcitabine.
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3

Establishment and Cultivation of Cholangiocarcinoma Cell Lines

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HuCC-T1 (human intrahepatic cholangiocarcinoma) cell line was obtained from the Health Science Research Resources Bank (Osaka, Japan), and SNU478 (human ampulla of Vater carcinoma), SNU1196 (human extrahepatic cholangiocarcinoma), and SNU245 (human common bile duct carcinoma) cells from the Korean Cell Line Bank (Seoul, Korea). All CC cells were maintained in RPMI 1640 medium supplemented with 10% fetal bovine serum and 1% antibiotics.
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4

BTC Cell Lines and Chemotherapeutics

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Nine human BTC cell lines were utilized in this research. The SNU245, SNU308, SNU478, SNU869, SNU1079, and SNU1196 cell lines were purchased from Korean Cell Line Bank (Seoul, Korea). The HuCCT-1 and TFK-1 cell lines were obtained from RIKEN BioResource Center (Ibaraki, Japan). A patient-derived cell line, SNU2670, was successfully established [19 (link)]. All cells were cultured in RPMI-1640 medium (Welgene Inc., Gyeongsan, Korea) containing 10% fetal bovine serum and 10 μg/mL gentamicin at 37°C incubator under 5% CO2. The ATR inhibitor AZD6738 was kindly provided by AstraZeneca (Macclesfield, Cheshire, UK). Gemcitabine, cisplatin, and 5-fluorouracil (5-FU) were purchased from Lilly Korea Co. (Seoul, Korea), JW Pharmaceutical Co. (Seoul, Korea), and Ildong Pharmaceutical Co. (Seoul, Korea), respectively.
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5

Establishment and Characterization of BTC Cell Lines

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Nine human BTC cell lines were utilized in this study. SNU245, SNU308, SNU478, SNU869, and SNU1196 cells were purchased from Korean Cell Line Bank (Seoul, Korea). HuCCT-1 and TFK-1 cells were obtained from RIKEN BioResource Center (Ibaraki, Japan). The patient-derived cell lines SNU2670 and SNU2773 were successfully established as described previously [10 (link)]. All cells were cultured in RPMI1640 medium (Welgen Inc., Gyeongsan, Korea) containing 10% fetal bovine serum and 10 μg/mL gentamicin at 37°C under 5% CO2. WEE1 (AZD1775), ATR (AZD6738), and ATM (AZD0156) inhibitors were kindly provided by AstraZeneca (Macclesfield, Cheshire, UK).
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6

CCA Cell Line SNU478 Culture and Compound Treatment

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The CCA cell line SNU478 was obtained from the Korea Cell Line Bank (Seoul, Korea). SNU478 cells cultured in Dulbecco’s modified eagle medium (DMEM; Gibco, Gaithersburg, MD, USA) supplied with 10% fetal bovine serum (FBS; RMBIO, Missoula, MT, USA) and 2% Antibiotic-Antimycotic solution (Gibco). SNU478 cell line was maintained in a humidified chamber with 5% CO2 at 37°C. Cordycepin (Fig. 1A) was kindly provided by Prof. Dr. Yeon Hee Seong (Laboratory of Pharmacology, College of Veterinary Medicine, Chungbuk National University, Cheongju, Korea). Gemcitabine was purchased from Sigma-Aldrich (Saint Louis, MO, USA). Cordycepin and Gemcitabine were dissolved in distilled water to prepare a stock solution at 200 mM and 5 mM, respectively, and diluted to testing concentration with medium before use. The control group received no treatment at all.
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7

Cultivating Biliary Tract Cancer Cell Lines

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Five human biliary tract cancer cell lines (SNU-245, SNU-308, SNU-478, SNU-1079, and SNU-1196) were procured from the Korea Cell Line Bank (Seoul, Korea). Cell lines were cultured in Rosewell Park Memorial Institute 1640 medium supplemented with 10% fetal bovine serum and 1% penicillin/streptomycin. Cells maintained in 5% CO2-humidified atmosphere at 37℃.
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8

Establishment of Human BTC Cell Lines

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A total of 11 human BTC cell lines were used in this study. SNU-245, SNU-308, SNU-478, SNU-869, SNU-1079, SNU-1196, and SNU-2823 cell lines were obtained from Korean Cell Line Bank, Seoul, Korea. HuCCT1 and TFK-1 cell lines were obtained from RIKEN BioResource Center, Ibaraki, Japan. HER2-amplified human BTC cell lines, SNU-2670 and SNU-2773, were established from tumor tissues from BTC patients using a previously described method [31 (link)].
All the cell lines were maintained in RPMI-1640 culture media supplemented with 10% fetal bovine serum (WELGENE Inc., Gyeongsan, Korea) and 10 μg/mL gentamicin in a humidified atmosphere containing 5% CO2 at 37°C.
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9

CCA Cell Line Culturing Protocol

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The HuCC-T1 CCA cell line was received from the Health Science Research Resources Bank (Osaka, Japan). SNU478, SNU245, and SNU 1196 CCA cell lines were obtained from Korean Cell Line Bank (Seoul, Korea). Cells were maintained in RPMI 1640 supplemented with 10% heat-inactivated FBS and 1% penicillin/streptomycin at 37°C in a 5% CO2 incubator.
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10

Culturing Cholangiocarcinoma Cell Lines

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The HuCCT1 cell line was purchased from the Health Science Research Resources Bank (Osaka, Japan), whereas other cholangiocarcinoma cell lines (SNU245, SNU308, SNU478, SNU869, SNU1079, and SNU1196) were purchased from the Korean Cell Line Bank (Seoul, Korea). The cell lines were grown in RPMI1640 supplemented with 10% fetal bovine serum (FBS), 25mM HEPES, and 100 μg/ml of penicillin/streptomycin in a 5% CO2 atmosphere at 37°C.
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