KU-19-19Homo sapiens (Human)Cancer cell line

Also known as: Keio University-19-19, KU1919, KU19-19, KU 19-19

🤖 AI SummaryBased on 11 publications

Quick Overview

Bladder cancer cell line with AKT1 mutations and cytokine production.

Detailed Summary

The KU-19-19 cell line is a human bladder cancer cell line derived from a 76-year-old male patient with metastatic transitional cell carcinoma. It is known for its ability to produce multiple cytokines, including granulocyte colony-stimulating factor (G-CSF), granulocyte-macrophage colony-stimulating factor (GM-CSF), macrophage colony-stimulating factor (M-CSF), stem cell factor (SCF), interleukin-6 (IL-6), and interleukin-8 (IL-8). This cell line exhibits constitutive activation of the AKT1 pathway due to the presence of the E17K mutation, which contributes to its proliferative and survival advantages. KU-19-19 has been used in studies investigating the role of cytokines in cancer progression and the effects of various treatments on cytokine production and cell proliferation. It is also utilized in research on the regulation of the NF-κB pathway and its impact on cell survival and cytokine expression.

Research Applications

AKT1 mutation analysisCytokine production studiesNF-κB pathway regulationDrug sensitivity testingTumor biology investigation

Key Characteristics

AKT1 E17K mutationConstitutive AKT1 activationCytokine secretion (G-CSF, GM-CSF, M-CSF, SCF, IL-6, IL-8)Autocrine growth via G-CSFNF-κB activation
Generated on 6/16/2025

Basic Information

Database IDCVCL_1344
SpeciesHomo sapiens (Human)
Tissue SourceUrinary bladder[UBERON:UBERON_0001255]

Donor Information

Age76
Age CategoryAdult
SexFemale

Disease Information

DiseaseBladder carcinoma
LineageBladder/Urinary Tract
SubtypeBladder Urothelial Carcinoma
OncoTree CodeBLCA

DepMap Information

Source TypeDSMZ
Source IDACH-000486_source

Known Sequence Variations

TypeGene/ProteinDescriptionZygosityNoteSource
MutationSimpleAKT1p.Glu17Lys (c.49G>A)Heterozygous-from parent cell line IHH-4

Haplotype Information (STR Profile)

Short Tandem Repeat (STR) profile for cell line authentication.

Amelogenin
X
CSF1PO
9,10
D13S317
11
D16S539
10,12
D18S51
17,20
D19S433
13,15
D21S11
30,32
D2S1338
19
D3S1358
16,17
D5S818
11,12
D7S820
10,12
D8S1179
10,13
FGA
22
Penta D
13
Penta E
10,15
TH01
7,8
TPOX
8,11
vWA
14,15
Gene Expression Profile
Gene expression levels and statistical distribution
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Full DepMap dataset with combined data across cell lines

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Publications

Pan-cancer proteomic map of 949 human cell lines.";

Robinson P.J., Zhong Q., Garnett M.J., Reddel R.R.

Cancer Cell 40:835-849.e8(2022).

Quantitative proteomics of the Cancer Cell Line Encyclopedia.";

Sellers W.R., Gygi S.P.

Cell 180:387-402.e16(2020).

Next-generation characterization of the Cancer Cell Line Encyclopedia.

Sellers W.R.

Nature 569:503-508(2019).

An interactive resource to probe genetic diversity and estimated ancestry in cancer cell lines.

Dutil J., Chen Z.-H., Monteiro A.N.A., Teer J.K., Eschrich S.A.

Cancer Res. 79:1263-1273(2019).

Systematic review: characteristics and preclinical uses of bladder cancer cell lines.

Zuiverloon T.C.M., de Jong F.C., Costello J.C., Theodorescu D.

Bladder Cancer 4:169-183(2018).

A landscape of pharmacogenomic interactions in cancer.";

Wessels L.F.A., Saez-Rodriguez J., McDermott U., Garnett M.J.

Cell 166:740-754(2016).

TCLP: an online cancer cell line catalogue integrating HLA type, predicted neo-epitopes, virus and gene expression.

Loewer M., Sahin U., Castle J.C.

Genome Med. 7:118.1-118.7(2015).

Identification of mutations in distinct regions of p85 alpha in urothelial cancer.

Knowles M.A.

PLoS ONE 8:E84411-E84411(2013).

Comprehensive mutation analysis of the TERT promoter in bladder cancer and detection of mutations in voided urine.

Hurst C.D., Platt F.M., Knowles M.A.

Eur. Urol. 65:367-369(2014).

The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity.

Morrissey M.P., Sellers W.R., Schlegel R., Garraway L.A.

Nature 483:603-607(2012).

Signatures of mutation and selection in the cancer genome.";

Deloukas P., Yang F.-T., Campbell P.J., Futreal P.A., Stratton M.R.

Nature 463:893-898(2010).

AKT1 mutations in bladder cancer: identification of a novel oncogenic mutation that can co-operate with E17K.

Knowles M.A.

Oncogene 29:150-155(2010).

Overexpression of IL-1ra gene up-regulates interleukin-1beta converting enzyme (ICE) gene expression: possible mechanism underlying IL-1beta-resistance of cancer cells.

Takayanagi A., Shimizu N.

Br. J. Cancer 81:277-286(1999).

Induction of apoptosis of cytokine-producing bladder cancer cells by adenovirus-mediated IkappaBalpha overexpression.

Nakamura H., Takayanagi A., Shimizu N.

Hum. Gene Ther. 10:37-47(1999).

Bladder carcinoma cell line KU-19-19-derived cytokines support proliferation of growth factor-dependent hematopoietic cell lines: modulation by phorbol ester, interferon-gamma and interleukin-1 beta.

Steube K.G., Meyer C., Tachibana M., Murai M., Drexler H.G.

Biochem. Biophys. Res. Commun. 242:497-501(1998).

Autocrine growth of transitional cell carcinoma of the bladder induced by granulocyte-colony stimulating factor.

Nishi T., Amano Y.

Cancer Res. 55:3438-3443(1995).

Web Resources