KU-19-19

Cat.No.: CSC-C0442

Species: Homo sapiens (Human)

Source: Bladder

Morphology: epithelial-like cells growing adherently in monolayers

Culture Properties: monolayer

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Cat.No.
CSC-C0442
Description
Established from the invasive transitional cell carcinoma of the bladder (grade 3, pT3b) of a 76-year-old man in 1993; described as secreting several hematopoietic cytokines and chorionic gonadotropin
Species
Homo sapiens (Human)
Source
Bladder
Recommended Medium
Culture Properties
monolayer
Morphology
epithelial-like cells growing adherently in monolayers
Karyotype
Human hypertriploid karyotype - 74(70-75)<3n>XXX, +1, +5, +6, -7, +9, -11, +12, +15, +16, -17, -18, +19, +21, -22, +2mar - add(1)(p32-34)/del(1)(p34), add(4)(q35)x1-2, del(5)(q14.2), add(6)(q11), del(11)(p14), add(12)(q24)/der(12)t(12;17)(q24;q12-22), add
Reference
Disease
Bladder Carcinoma
Quality Control
Mycoplasma: negative in DAPI, microbiological culture, RNA hybridization assays
Immunology: cytokeratin +, cytokeratin-7 +, cytokeratin-8 +, cytokeratin-17 +, cytokeratin-18 +, cytokeratin-19 +, desmin -, endothel -, EpCAM -, GFAP -, neurofilament -, vim
Storage and Shipping
Frozen with 70% medium, 20% FBS, 10% DMSO at about 1-2 x 10^6 cells/ampoule; ship in dry ice; store in liquid nitrogen
Synonyms
KU 19-19; KU19-19; KU1919; Keio University-19-19
Citation Guidance
If you use this products in your scientific publication, it should be cited in the publication as: Creative Bioarray cat no. If your paper has been published, please click here to submit the PubMed ID of your paper to get a coupon.

KU-19-19 is a human bladder carcinoma cell line with distinct advantages for studying transitional cell carcinoma biology, tumor microenvironment interactions, and cytokine-mediated signaling. This epithelial cell line was established in 1993 by a Japanese research team from an invasive transitional cell carcinoma of the bladder (grade 3, pT3b) obtained from a 76-year-old male patient who exhibited marked leukocytosis. The cell line grows adherently as epithelial-like cells in monolayers under standard culture conditions, with a doubling time of approximately 48 hours.

A defining feature of KU-19-19 cells is their ability to constitutively produce and secrete multiple hematopoietic growth factors. Conditioned medium from KU-19-19 cultures contains high levels of granulocyte colony-stimulating factor (G-CSF, exceeding 5 ng/mL), as well as GM-CSF, M-CSF, stem cell factor (SCF), interleukin-6 (IL-6), and interleukin-8 (IL-8). These secreted factors vigorously stimulate proliferation of growth factor-dependent hematopoietic cell lines in a dose-dependent manner, confirming their functional biological activity. This robust secretory profile makes KU-19-19 a practical source for G-CSF purification and a versatile platform for tumor-hematopoietic cell interaction studies.

KU-19-19 cells exhibit constitutive activation of NF-κB, a transcription factor frequently dysregulated in advanced malignancies. When implanted, these cells form tumors in nude mice, associated with severe neutrophilia in peripheral blood, recapitulating the paraneoplastic leukocytosis observed in the original patient. Numerous studies have leveraged KU-19-19 cells to evaluate drug candidates such as the NF-κB inhibitor DHMEQ and natural compounds active against bladder cancer progression, demonstrating their broad utility in anticancer research.

Cytotoxicity of 212Pb-Labeled Anti-PTK7 Antibody in 2D Adherent and 3D Multicellular Bladder Cancer Models

This study evaluated the preclinical efficacy of [212Pb]Pb-TCMC-chOI-1, a 212Pb-labeled antibody targeting PTK7, for targeted alpha-emitting radionuclide therapy in bladder cancer using 2D adherent cultures (clonogenic assay) and 3D multicellular spheroid models (spheroid growth inhibition).

[212Pb]Pb-TCMC-chOI-1 treatment resulted in activity- and time-dependent cytotoxicity, with enhanced sensitivity observed in cell lines with higher PTK7 levels. In clonogenic assays, the activity concentration required for 50% growth reduction was 48-74 kBq/mL, corresponding to 22-51 bound and 9-16 internalized 212Pb atoms per cell. In 3D models, similar therapeutic effects were observed despite significantly lower activities (values of approximately 1 and 30 kBq/mL for KU-19-19 and 647-V cells, respectively), suggesting a more pronounced cross-fire effect. Flow cytometry demonstrated treatment-induced DNA damage, cell cycle perturbations and cell death, with response patterns correlating with overall treatment sensitivity. RT-112 and KU-19-19 cells showed superior responses compared to 647-V and T-24 cells, consistent with their higher PTK7 expression.

These findings support PTK7 as a therapeutic target for bladder cancer and demonstrate the potential of [212Pb]Pb-TCMC-chOI-1 for targeted alpha-emitting radionuclide therapy.

Cytotoxicity of [212Pb]Pb-TCMC-chOI-1 in 3D multicellular models.

Fig. 1. Growth inhibition of bladder cancer spheroids treated with [212Pb]Pb-TCMC-mAbs (Lindland, Kim, and Asta Juzeniene. 2025).

Assessment of cell viability, cell cycle progression, and DNA damage.

Fig. 2. Cell viability, apoptosis, DNA damage, and mitotic analysis in KU-19-19 and 647-V cells following [212Pb]Pb-TCMC-chOI-1 treatment (Lindland, Kim, and Asta Juzeniene. 2025).

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