MDAH-2774 (CRL-10303), TOV-21G (CRL-11730), OV-90 (CRL-11732), SKOV-3 (HTB-77), NIH:OVCAR-3 (HTB-161), and Met5a (CRL-9444) cells were obtained from the American Type Culture Collection (ATCC); OVSAHO (JCRB1046) and KURAMOCHI (JCRB0098) cells were from the JCRB Cell Bank; COV-362 [ECACC (European Collection of Authenticated Cell Cultures) 07071910] cells were from Sigma-Aldrich; and OVCAR-8 and OVCAR-4 cells were from the National Cancer Institute Developmental Therapeutics Program Tumor Repository. All these cell lines were maintained in RPMI 1640 medium (Sigma-Aldrich). Breast cancer cell lines MDA-MB 468 (HTB-132), BT-549 (HTB-122), MCF-7 (HTB-22), and T47D (HTB-133) were obtained from ATCC and maintained in Dulbecco’s modified Eagle’s medium (DMEM) (Sigma-Aldrich). Primary epithelial OC cell lines (31) were provided by D.C.C.-T. and maintained in DMEM/F12 (Gibco). Human embryonic kidney (HEK) 293/T17 cells (ATCC, CRL-11268) used for overexpression strategies and 293FT cells (Invitrogen) used for lentivirus production following the manufacturer’s instructions (Clontech) were grown in DMEM high glucose (Sigma-Aldrich). Met5a cells were grown in RPMI 1640 medium (Sigma-Aldrich) with insulin (870 nM), epidermal growth factor (EGF (3.3 nM), and hydrocortisone (400 nM). All media were supplemented with 10% heat-inactivated fetal bovine serum and 1% penicillin/streptomycin. All cell lines were grown in standard conditions at 37°C and 5% CO2. All cell lines were routinely authenticated in our laboratory using the Cell ID TM System (Promega) protocol and using GeneMapper ID version 3.2.1 to identify DNA short tandem repeat profiles (last authentication was on 29 May 2018).

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