Caki-2Homo sapiens (Human)Cancer cell line

Also known as: CAKI2, Caki2, Caki 2, CAKI 2, caki-2, CaKi-2, CAKI-2

🤖 AI SummaryBased on 16 publications

Quick Overview

Caki-2 is a renal cell carcinoma cell line used in cancer research.

Detailed Summary

Caki-2 is a renal cell carcinoma (RCC) cell line derived from a clear cell RCC tumor. It is widely used in research to study the molecular mechanisms of RCC, including genetic alterations and therapeutic responses. The cell line has been characterized for its genomic features, such as mutations in the VHL gene and other key oncogenes. Caki-2 is utilized in studies involving drug screening, immunotherapy, and understanding tumor progression. Its utility in preclinical models makes it a valuable tool for investigating RCC biology and potential treatment strategies.

Research Applications

Genomic studiesDrug screeningImmunotherapy researchTumor progression analysis

Key Characteristics

Clear cell RCC originVHL gene mutationsUsed in preclinical models
Generated on 6/15/2025

Basic Information

Database IDCVCL_0235
SpeciesHomo sapiens (Human)
Tissue SourceKidney[UBERON:UBERON_0002113]

Donor Information

Age69
Age CategoryAdult
SexMale
Racecaucasian

Disease Information

DiseasePapillary renal cell carcinoma
LineageKidney
SubtypePapillary Renal Cell Carcinoma
OncoTree CodePRCC

DepMap Information

Source TypeATCC
Source IDACH-000234_source

Haplotype Information (STR Profile)

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

Amelogenin
X,Y
CSF1PO
10,12
D10S1248
14,16
D12S391
19,23
D13S317
10
D16S539
9,13
D18S51
17
D19S433
13,14
D1S1656
12,14
D21S11
27,31
D22S1045
15
D2S1338
17,20
D2S441
14
D3S1358
14
D5S818
11
D7S820
12
D8S1179
10
FGA
22
Penta D
10,13
Penta E
7,17
TH01
6
TPOX
9,11
vWA
16,17
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

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).

Analysis of renal cancer cell lines from two major resources enables genomics-guided cell line selection.

Hsieh J.J.-D., Hakimi A.A.

Nat. Commun. 8:15165.1-15165.10(2017).

Characterization of human cancer cell lines by reverse-phase protein arrays.

Liang H.

Cancer Cell 31:225-239(2017).

Choosing the right cell line for renal cell cancer research.";

Czarnecka A.M.

Mol. Cancer 15:83.1-83.15(2016).

Data for identification of GPI-anchored peptides and omega-sites in cancer cell lines.

Masuishi Y., Kimura Y., Arakawa N., Hirano H.

Data Brief 7:1302-1305(2016).

Identification of glycosylphosphatidylinositol-anchored proteins and omega-sites using TiO2-based affinity purification followed by hydrogen fluoride treatment.

Masuishi Y., Kimura Y., Arakawa N., Hirano H.

J. Proteomics 139:77-83(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).

A resource for cell line authentication, annotation and quality control.

Neve R.M.

Nature 520:307-311(2015).

A comprehensive transcriptional portrait of human cancer cell lines.

Settleman J., Seshagiri S., Zhang Z.-M.

Nat. Biotechnol. 33:306-312(2015).

Loss of PBRM1 expression is associated with renal cell carcinoma progression.

Pawlowski R., Muhl S.M., Sulser T., Krek W., Moch H., Schraml P.

Int. J. Cancer 132:E11-E17(2013).

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).

Downregulation of SAV1 plays a role in pathogenesis of high-grade clear cell renal cell carcinoma.

Mimata H., Seto M., Moriyama M.

BMC Cancer 11:523.1-523.10(2011).

A genome-wide screen for microdeletions reveals disruption of polarity complex genes in diverse human cancers.

Haber D.A.

Cancer Res. 70:2158-2164(2010).

Detection of DNA copy number changes and oncogenic signaling abnormalities from gene expression data reveals MYC activation in high-grade papillary renal cell carcinoma.

Kahnoski R., Yang X.-M.J., Teh B.T.

Cancer Res. 67:3171-3176(2007).

Allogeneic hematopoietic cell transplantation for metastatic renal cell carcinoma after nonmyeloablative conditioning: toxicity, clinical response, and immunological response to minor histocompatibility antigens.

Otterud B.E., Leppert M.F., Storb R., Sandmaier B.M.

Clin. Cancer Res. 10:7799-7811(2004).

Expression of the SART1 tumor rejection antigen in renal cell carcinoma.

Yoshizumi O., Itoh K.

Urol. Res. 28:178-184(2000).

Combined LOH/CGH analysis proves the existence of interstitial 3p deletions in renal cell carcinoma.

Imreh S., Klein G., Zabarovsky E.R.

Oncogene 19:1392-1399(2000).

Contribution of chromosome 9p21-22 deletion to the progression of human renal cell carcinoma.

Mishina M., Habuchi T., Takahashi R., Sugiyama T., Yoshida O.

Jpn. J. Cancer Res. 86:795-799(1995).

Presence of glycogen and growth-related variations in 58 cultured human tumor cell lines of various tissue origins.

Rousset M., Zweibaum A., Fogh J.

Cancer Res. 41:1165-1170(1981).

Distinction of seventy-one cultured human tumor cell lines by polymorphic enzyme analysis.

Wright W.C., Daniels W.P., Fogh J.

J. Natl. Cancer Inst. 66:239-247(1981).

Cell surface antigens of human ovarian and endometrial carcinoma defined by mouse monoclonal antibodies.

Mattes M.J., Cordon-Cardo C., Lewis J.L. Jr., Old L.J., Lloyd K.O.

Proc. Natl. Acad. Sci. U.S.A. 81:568-572(1984).

Human urologic cancer cell lines.";

Williams R.D.

Invest. Urol. 17:359-363(1980).

Human tumor lines for cancer research.";

Fogh J.

Cancer Invest. 4:157-184(1986).

Absence of HeLa cell contamination in 169 cell lines derived from human tumors.

Fogh J., Wright W.C., Loveless J.D.

J. Natl. Cancer Inst. 58:209-214(1977).

Cultivation, characterization, and identification of human tumor cells with emphasis on kidney, testis, and bladder tumors.

Fogh J.

Natl. Cancer Inst. Monogr. 49:5-9(1978).

One hundred and twenty-seven cultured human tumor cell lines producing tumors in nude mice.

Fogh J., Fogh J.M., Orfeo T.

J. Natl. Cancer Inst. 59:221-226(1977).

New human tumor cell lines.";

Fogh J., Trempe G.L.

(In book chapter) Human tumor cells in vitro; Fogh J. (eds.); pp.115-159; Springer; New York; USA (1975).