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OVKATE is a cell line derived from human ovarian carcinoma. It is maintained and provided by the Japanese Collection of Research Bioresources Cell Bank for research purposes.

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7 protocols using ovkate

1

Comprehensive Ovarian Cancer Cell Line Protocols

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RMG-I [32] (link), OVMANA [33] (link), OVTOKO [34] (link), OVISE [34] (link), OVSAHO [33] (link), and OVKATE [33] (link) cells were obtained from the Japanese Collection of Research Bioresources Cell Bank. OVCAR-3 cells [35] (link) were obtained from the RIKEN BioResource Center. PEO1, PEO4, PEO14, PEO23 [17] (link), and A2780 [36] (link) cells were purchased from the European Collection of Cell Cultures, and TOV21G [37] (link) and ES-2 [38] (link) cells were purchased from the American Type Culture Collection. RMG-I cells were cultured in Ham’s F12 medium supplemented with 10% fetal bovine serum, ES-2 cells in McCoy’s 5a medium supplemented with 10% fetal bovine serum, TOV21G cells in MCDB105/Medium 199 (1∶1) supplemented with 10% fetal bovine serum, and HeLa cells in Dulbecco’s modified Eagle’s medium (DMEM) supplemented with 10% fetal bovine serum. All other cell lines (A2780, OVCAR-3, OVMANA, OVTOKO, OVISE, OVSAHO, OVKATE, PEO1, PEO4, PEO14, and PEO23) were cultured in RPMI-1640 medium supplemented with 10% fetal bovine serum and 1 mM sodium pyruvate (Gibco, Grand Island, NY, USA).
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2

Ovarian Cancer Cell Line Cultivation

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The human ovarian serous adenocarcinoma cell lines SHIN‐3,
12 (link) KOC‐2S,
13 (link) and TU‐OS‐4
14 (link) were provided by the respective establishers. The human ovarian serous adenocarcinoma cell lines OVSAHO and OVKATE were purchased from the Japanese Collection of Research Bioresources (JCRB; Osaka, Japan). The human ovarian cancer cell line SKOV‐3 was purchased from the American Type Culture Collection (ATCC, Manassas, VA, USA). The human breast adenocarcinoma cell line MCF‐7 was purchased from RIKEN BioResource Research Center (Tsukuba, Japan). The cells were cultured in Dulbecco's Modified Eagle Medium/F12 (DMEM/F12; Thermo Fisher Scientific, Inc., Waltham, MA, USA) supplemented with 10% heat‐inactivated fetal bovine serum (FBS; Sigma‐Aldrich; Merck KGaA, Darmstadt, Germany) and 1% penicillin/streptomycin (Thermo Fisher Scientific, Inc.) at 37°C in a humidified atmosphere under 5% CO2.
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3

Ovarian Cancer Cell Line Cultivation

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The OVTOKO, OVISE, OVMANA, RMG-I, OVSAHO, OVKATE, and OV1063 lines were purchased from the Japanese Collection of Research Bioresources (JCRB) Cell Bank (Osaka, Japan). The JHOC-7, JHOC-9, HTOA, JHOS-2, JHOS-3, and JHOS-4 cell lines were purchased from the RIKEN Cell Bank (Ibaraki, Japan). The TOV-21, ES-2, and SKOV3 cell lines were from the American Type Culture Collection (Manassas, VA). OVISE, OVTOKO, TOV-21G and ES2 were cultured in RPMI1640 medium containing 10% fetal bovine serum (FBS). OVMANA was cultured in RPMI medium containing 20% FBS, JHOC-7 in DMEM/F12 medium containing 10% FBS, JHOC-9 and RMG-I in DMEM/F12 medium containing 20% FBS, and SKOV3 in DMEM containing 10% FBS. The OVSAHO, OVKATE, OV1063, HTOA, JHOS-2, JHOS-3, and JHOS-4 lines were cultured in DMEM medium containing 10% FBS. The histological subtype of the SKOV3 cells was not unambiguously defined even after extensive analysis, although it was confidently identified as clear cell adenocarcinoma [22] (link). The immortalized epithelial cell line from an ovarian endometrial cyst was a generous gift from Dr. Satoru Kyo [23] (link).
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4

Cell Line Sourcing and Mycoplasma Testing

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The cell lines NCI-H661, NCI-H522, NCI-146, KLE, Caov4, NCI-H716, HuTu80, HCC 1419, Calu-3, 22Rv1, U-118MG, A-673, SK-N-MC, MDA-MB-231, A549, K-562, L Wnt-5A, and L cells were obtained from the American Type Culture Collection (ATCC). The cells, Cov434 (cat. no. 07071909), COV318 (cat. no. 07071903), and 1321N1 (cat. no. 86030402) were obtained from Sigma, HEC-59 (cat. no. C0026001) from AddexBio and OVKATE and OVSAHO from the Japanese Collection of Research Bioresources (JCRB) Cell Bank. All cells were tested for mycoplasma contamination before use with the Universal Mycoplasma Detection Kit (ATCC 30-1012K).
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5

Diverse Ovarian Cancer Cell Lines

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HEK293T, OV90, HCT116, HT-29, ZR75-30, HCC1954 and BT549 were purchased from American Type Culture Collection (ATCC). OVKATE was purchased from JCRB Cell Bank. OV56, A2780 and IGROV1 were purchased from Sigma. COLO678 was purchased from Leibniz Institute DSMZ. Human ovarian PARP inhibitor and cisplatin-resistant cancer cell lines, PEO1/ABT-888 and OVCAR-1/Cisplatin and their parental cell lines, were gifts from Prof. Scott Kaufmann (Department of Oncology, Mayo Clinic). Cells were maintained under recommended culture conditions. PEO1/ABT-888 and OVCAR-1/Cisplatin were cultured in the media supplemented with 10 μM ABT-888 and 0.5 μg cisplatin, respectively. Cells were regularly tested for mycoplasma contamination.
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6

Authenticated Ovarian Cancer Cell Lines

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OVCAR3, OVCAR5, SKOV3, and ES2 cells were purchased from the American Type Culture Collection (ATCC, Manassas, VA, USA). OVCAR4 cells were gifted from Dr. Joanna Burdette (University of Illinois at Chicago). KURAMOCHI, OVKATE and OVSAHO were purchased from the JCRB cell bank (Osaka, Japan). SKOV3.ip1 cells were purchased from the cell bank at The University of Texas MD Anderson Cancer Center. All cells were authenticated by short tandem repeat (STR) analysis and passaged within 6 months of receipt. All cells were tested routinely for cell proliferation and BrdU incorporation as well as mycoplasma contamination. All cell lines exhibited similar morphology, characteristic growth rates, and remained negative for mycoplasma contamination throughout all experiments. OVCAR4, KURAMOCHI, OVKATE and OVSAHO cells were grown in RPMI 1640 with 10% FBS and penicillin/streptomycin, and other cells were cultured in DMEM with 10% FBS, 2mM glutamine and penicillin/streptomycin. All cell lines were grown in a humidified incubator at 37°C and constant 5% CO2.
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7

LRRK2 Regulation of DNA Repair Pathways

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The human U2OS, HEK293T, OVCAR8, and OVCAR10 were purchased from ATCC. PEO1 and OV56 were bought from Sigma. OVKATE cells purchased from JCRB Cell Bank. Cells were immersed in McCoy's 5A, Dulbecco's Modified Eagle's Medium (DMEM), or RPMI1640, or added with 10% fetal bovine serum (FBS) in 5% CO2 at 37°C. pDEST51‐LRRK2 was purchased from Addgene (#25080). Full‐length LRRK2 was constructed into pLVX3 lentiviral vector and then lentivirus was packaged, and OVCAR10 cells were infected with the virus and selected with puromycin for 10 days to establish stable cell lines. pCMV‐Myc‐RAD51 was given by Dr. Junjie Chen (University of Texas MD Anderson Cancer Center). pCHMWS‐FLAG‐LRRK2 and mutations (K1906M,G2019S, and pS935/910) were gifts from Dr. Cookson (Molecular Genetics Section, Laboratory of Neurogenetics, National Institute on Aging). Anti‐RAD51 (GTX100469) antibody was purchased from GeneTex. Anti‐BRCA1 (SC‐6954), Antigreen fluorescent protein [GFP] (SC‐9996), Anti‐RPA2 (SC‐56770), and Anti‐Myc (sc‐40, mouse) antibodies were sold by Santa Cruz Biotechnology. Anti‐BRCA2 (pS3291,AB9986) was bought from sigma. Anti‐BRCA2 (OP95‐100UG) was purchased from Millipore Anti‐V5 (SV5‐Pk1) antibody, Anti‐LRRK2(pS910)(ab133450), and Anti‐LRRK2(pS935)(ab133449) were purchased from Abcam.
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