TanoueHomo sapiens (Human)Cancer cell line

Also known as: TANOUE

🤖 AI SummaryBased on 6 publications

Quick Overview

Human B-lineage acute lymphoblastic leukemia cell line with potential for mixed lineage characteristics.

Detailed Summary

The Tanoue cell line, derived from a B-lineage acute lymphoblastic leukemia (ALL) patient, is notable for its expression of myeloid surface antigens and the ability to respond to granulocyte colony-stimulating factor (G-CSF). This cell line has been used to study the effects of G-CSF receptor expression on myeloid differentiation and proliferation. Research indicates that exogenous expression of the G-CSF receptor can induce myeloid characteristics in ALL cells, suggesting potential applications in understanding mixed lineage leukemias. The cell line has also been utilized to investigate the relationship between G-CSF receptor expression and cell responsiveness to G-CSF in terms of proliferation and differentiation.

Research Applications

Study of G-CSF receptor function in leukemiaInvestigation of mixed lineage leukemia characteristicsAnalysis of myeloid differentiation in B-cell ALLEvaluation of G-CSF responsiveness in leukemic cells

Key Characteristics

Expression of myeloid surface antigensAbility to respond to G-CSFPotential for mixed lineage characteristicsExogenous G-CSF receptor expression induces myeloid features
Generated on 6/17/2025

Basic Information

Database IDCVCL_1852
SpeciesHomo sapiens (Human)
Tissue SourcePeripheral blood[UBERON:UBERON_0000178]

Donor Information

Age11
Age CategoryPediatric
SexMale
Subtype FeaturesBCL2/MYC

Disease Information

DiseasePrecursor B-cell acute lymphoblastic leukemia
LineageLymphoid
SubtypeB-Lymphoblastic Leukemia/Lymphoma
OncoTree CodeBLL

DepMap Information

Source TypeDSMZ
Source IDACH-001669_source

Known Sequence Variations

TypeGene/ProteinDescriptionZygosityNoteSource
MutationSimpleTP53p.Met246Thr (c.737T>C)Heterozygous-Unknown, PubMed=15901131

Haplotype Information (STR Profile)

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

Amelogenin
X,Y
CSF1PO
11,12
D13S317
11,12
D16S539
10,12,13,14
D18S51
13,14
D19S433
15,16
D21S11
29,30
D2S1338
18,19
D3S1358
15,16
D5S818
10,11,12
D7S820
10,11
D8S1179
14,15
FGA
19,22,23
Penta D
11,13
Penta E
14,18,19
TH01
7,10
TPOX
11
vWA
14,18,19
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

Integrative multi-omics and drug response profiling of childhood acute lymphoblastic leukemia cell lines.

Lehtio J., Vesterlund M., Jafari R.

Nat. Commun. 13:1691.1-1691.19(2022).

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

Liang H.

Cancer Cell 31:225-239(2017).

Comprehensive cytogenetic and molecular cytogenetic analysis of 44 Burkitt lymphoma cell lines: secondary chromosomal changes characterization, karyotypic evolution, and comparison with primary samples.

Vettorazzi E., Bokemeyer C., Dierlamm J.

Genes Chromosomes Cancer 53:497-515(2014).

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).

JAK2 V617F tyrosine kinase mutation in cell lines derived from myeloproliferative disorders.

Quentmeier H., MacLeod R.A.F., Zaborski M., Drexler H.G.

Leukemia 20:471-476(2006).

Correlation between DNA alterations and p53 and p16 protein expression in cancer cell lines.

Murai Y., Hayashi S., Takahashi H., Tsuneyama K., Takano Y.

Pathol. Res. Pract. 201:109-115(2005).

Gene expression profiling of leukemic cell lines reveals conserved molecular signatures among subtypes with specific genetic aberrations.

Fioretos T.

Leukemia 19:1042-1050(2005).

Exogenous expression of human granulocyte colony-stimulating factor receptor in a B-lineage acute lymphoblastic leukemia cell line: a possible model for mixed lineage leukemia.

Shimosaka A., Matsuda I.

Leuk. Res. 19:249-256(1995).

The leukemia-lymphoma cell line factsbook.";

Drexler H.G.

(In book) ISBN 9780122219702; pp.1-733; Academic Press; London; United Kingdom (2001).

Web Resources