The largest database of trusted experimental protocols

21 protocols using hucct1

1

Characterization of Biliary Tract Cancer Cell Lines

Check if the same lab product or an alternative is used in the 5 most similar protocols
Experiments were performed using 16 BTC cell lines. Thirteen cell lines were previously established from Japanese patients with BTC15 (link), 16 (link), 17 (link): NCC‐BD1, NCC‐BD2, NCC‐BD3, NCC‐BD4‐1, and NCC‐BD4‐2 were derived from ECC, and NCC‐CC1, NCC‐CC3‐1, NCC‐CC3‐2, NCC‐CC4‐1, NCC‐CC4‐2, NCC‐CC5, NCC‐CC6‐1, and NCC‐CC6‐2 were derived from ICC. Moreover, we used three BTC cell lines (TKKK, OZ, and HuCCT1) purchased from Riken BioResource Center or from the Japanese Collection of Research Bioresources. OZ and HuCCT1 were derived from ECC, whereas TKKK was derived from ICC. TKKK and OZ cells were cultivated in DMEM plus 10% FBS and antibiotics, whereas the remaining 14 cell lines were cultivated in RPMI‐1640 medium plus 10% FBS and antibiotics. NCC‐BD2, NCC‐BD3, NCC‐BD4‐1, NCC‐CC1, NCC‐CC3‐1, NCC‐CC6‐1, and TKKK cells were cultured on collagen I‐coated dishes. The remaining nine cell lines were cultivated on normal culture dishes. All cells were kept at 37℃ in an atmosphere of 5% CO2.
+ Open protocol
+ Expand
2

Culturing Cholangiocarcinoma Cell Lines

Check if the same lab product or an alternative is used in the 5 most similar protocols
Two human cholangiocarcinoma cell lines (RBE and HUCCT1) were purchased from RIKEN Bioresource Center (Tsukuba, Ibaraki, Japan) and cultured in RPMI-1640 medium containing 10% fetal bovine serum in a 5% CO2 incubator at 37 °C.
+ Open protocol
+ Expand
3

Human Cholangiocarcinoma Cell Culture

Check if the same lab product or an alternative is used in the 5 most similar protocols
HuCCT1 (RCB‐1960) and Huh28 (RCB‐1943) CCA cell lines were purchased at the RIKEN BioResource Center (Tsukuba‐shi, Japan). Cells were grown in Roswell Park Memorial Institute 1640 medium (HuCCT1) or minimal essential medium (Huh28) supplemented with 100 U/mL penicillin, 100 μg/mL streptomycin, and 10% fetal bovine serum. HCC cell lines were purchased from ATCC and cultured as described.15 LX2 cells were grown as described.16 Freshly isolated human hepatocytes were purchased from Biopredic International (St. Grégoire, France). Cells were cultured at 37 °C in a 5% CO2 atmosphere, and overnight serum starvation was performed before each treatment. Unless otherwise specified, cells were treated with 1 ng/mL recombinant human TGFβ (R&D Systems, Minneapolis, MN) and 10 µM TGFβ inhibitors (Sigma‐Aldrich, St. Louis, MO).
+ Open protocol
+ Expand
4

Culturing Human Colorectal Cancer Cell Lines

Check if the same lab product or an alternative is used in the 5 most similar protocols
RBE, HuCCT1, and TFK‐1 human CC cell lines were purchased from RIKEN BioResource Center (Tsukuba, Japan) and cultured in RPMI‐1640 medium (Sigma‐Aldrich, St. Louis, MO, USA) supplemented with 10% heat‐inactivated FBS (Sigma‐Aldrich) and 1% penicillin/streptomycin (Thermo Fisher Scientific, Waltham, MA, USA) at 37°C and 5% CO2. Cisplatin was purchased from Nippon Kayaku (Tokyo, Japan) and diluted with cell culture medium before use in in vitro experiments.
+ Open protocol
+ Expand
5

BTC Cell Lines and Chemotherapeutics

Check if the same lab product or an alternative is used in the 5 most similar protocols
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.
+ Open protocol
+ Expand
6

Establishment and Characterization of BTC Cell Lines

Check if the same lab product or an alternative is used in the 5 most similar protocols
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).
+ Open protocol
+ Expand
7

HuCCT1 Cell Line Culture

Check if the same lab product or an alternative is used in the 5 most similar protocols
The human CCA cell line HuCCT1 (Riken Bioresource Research Center, Japan) was grown in RPMI 1640 medium supplemented with 10% fetal bovine serum at 37°C in a 5% CO2 humidified atmosphere. For signal transduction experiments, cells were starved overnight in a serum-free medium.
+ Open protocol
+ Expand
8

Cholangiocarcinoma Cell Line Culture

Check if the same lab product or an alternative is used in the 5 most similar protocols
The human cholangiocarcinoma cell lines HuCCT-1, HCCC-9810 and RBE were purchased from the RIKEN bioresource Center (Saitama-ken, Japan). The TFK-1 cell line was purchased from DSMZ (Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH, Braunschweig, Germany). Cells were cultured in Roswell Park Memorial Institute 1640 (RPMI 1640, Thermo Fisher Scientific, New York, USA) medium with 10% fetal bovine serum (FBS, Gibco, Thermo Fisher Scientific) at 37°C in a humidified atmosphere comprising 5% CO2. All cell lines were tested for mycoplasma contamination (Genecreate Biological engineering Co., Ltd, Wuhan, China).
+ Open protocol
+ Expand
9

Establishing and Characterizing Normal Human Cholangiocytes

Check if the same lab product or an alternative is used in the 5 most similar protocols
Primary cultures of normal human cholangiocytes (NHC) were established, characterized and cultured as previously described (Urribarri et al, 2014 (link)). HuCCT1 and Huh28 CCA cell lines were purchased from RIKEN BioResource Center (Tsukuba-shi, Japan) and CCLP1, Egi-1, SG231, TFK1, Sk-ChA-1 and Mz-ChA-1 were provided by Laura Fouassier (Paris, France). HepG2/C3A and HEK293T were purchased from ATCC (www.lgcstandards-atcc.org). Serum-starved cells were stimulated with the indicated concentrations of human recombinant TGFβ1 (R&D Systems) and for the indicated time periods as shown in the figures and figure legends.
+ Open protocol
+ Expand
10

Culturing Human CCA Cell Lines

Check if the same lab product or an alternative is used in the 5 most similar protocols
Human CCA cell lines HuCCT1 and TFK-1 were purchased from the RIKEN BRC (Ibaraki, Japan). Cells were cultured in RPMI-1640 (Gibco, NY) with 10 % fetal bovine serum (FBS) (Gibco, NY) and 100 U/mL penicillin and 100 µg/mL streptomycin (Invitrogen, MA) and incubated at 37 °C in a 5 % CO2 humidified atmosphere.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!