MHH-CALL-2Homo sapiens (Human)Cancer cell line

Also known as: MHHCALL2, MHH-CALL2, Mhh-Call 2

🤖 AI SummaryBased on 7 publications

Quick Overview

MHH-CALL-2 is a human cell line derived from acute myeloid leukemia, characterized by the JAK2 V617F mutation and specific chro...

Detailed Summary

MHH-CALL-2 is a human cell line established from a patient with acute myeloid leukemia (AML). It is notable for harboring the JAK2 V617F mutation, a key driver in myeloproliferative disorders. This cell line exhibits specific chromosomal abnormalities, including losses of heterozygosity (LOH) on chromosome 9p, which are associated with the pathogenesis of myeloid malignancies. The presence of the JAK2 V617F mutation and LOH on 9p makes MHH-CALL-2 a valuable model for studying the molecular mechanisms underlying myeloproliferative disorders and AML. It is also used in research to investigate the role of JAK2 signaling in leukemogenesis and to test therapeutic strategies targeting JAK2 mutations.

Research Applications

Study of JAK2 V617F mutation in myeloproliferative disordersInvestigation of chromosomal abnormalities in AMLAnalysis of LOH on chromosome 9p in myeloid malignanciesDevelopment of targeted therapies for JAK2-mutated leukemias

Key Characteristics

JAK2 V617F mutationLoss of heterozygosity on chromosome 9pRelevance to myeloproliferative disorders and AML
Generated on 6/17/2025

Basic Information

Database IDCVCL_1409
SpeciesHomo sapiens (Human)
Tissue SourcePeripheral blood[UBERON:UBERON_0000178]

Donor Information

Age15
Age CategoryPediatric
SexFemale
Racecaucasian
Subtype FeaturesNear haploid

Disease Information

DiseasePrecursor B-cell acute lymphoblastic leukemia
LineageLymphoid
SubtypeB-Lymphoblastic Leukemia/Lymphoma with Hypodiploidy
OncoTree CodeBLLHYPO

DepMap Information

Source TypeDSMZ
Source IDACH-000020_source

Haplotype Information (STR Profile)

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

Amelogenin
X
CSF1PO
14
D13S317
8
D16S539
14
D18S51
12,14
D19S433
14
D21S11
29,30
D2S1338
20
D3S1358
15
D5S818
12
D7S820
9
D8S1179
12
FGA
23
Penta D
9,12
Penta E
12
TH01
8
TPOX
11
vWA
18
Gene Expression Profile
Gene expression levels and statistical distribution
Loading cohorts...
Full DepMap dataset with combined data across cell lines

Loading gene expression data...

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).

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).

Screening human cell lines for viral infections applying RNA-Seq data analysis.

Uphoff C.C., Pommerenke C., Denkmann S.A., Drexler H.G.

PLoS ONE 14:E0210404-E0210404(2019).

Profiling the B/T cell receptor repertoire of lymphocyte derived cell lines.

Yang H.H., Koeffler H.P.

BMC Cancer 18:940.1-940.13(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).

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).

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).

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

Fioretos T.

Leukemia 19:1042-1050(2005).

Occurrence of TEL-AML1 fusion resulting from (12;21) translocation in human early B-lineage leukemia cell lines.

Janssen J.W.G., Drexler H.G.

Leukemia 11:441-447(1997).

The leukemia-lymphoma cell line factsbook.";

Drexler H.G.

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