OCI-AML-2Homo sapiens (Human)Cancer cell line

Also known as: Ontario Cancer Institute-Acute Myeloid Leukemia-2, AML-2, OCIAML2, OCI AML2, OCI/AML2, OCI-AML2, OCIAML-2, OCI/AML-2

🤖 AI SummaryBased on 9 publications

OCI-AML2

Quick Overview

Human AML cell line with JAK2 V617F mutation for cancer research.

Detailed Summary

The OCI-AML2 cell line is a human acute myeloid leukemia (AML) cell line derived from a patient with a history of myeloproliferative disorders (MPD) or myelodysplastic syndrome (MDS). It is characterized by the presence of the JAK2 V617F mutation, which is a key driver in myeloproliferative disorders. This cell line is used in research to study the molecular mechanisms of JAK2 mutations and their role in leukemogenesis. The OCI-AML2 cell line has been utilized in studies investigating the effects of JAK2 inhibition and the genetic alterations associated with MPD and MDS. It is also part of large-scale genomic and transcriptomic studies to understand the complexity of AML and its subtypes.

Research Applications

Study of JAK2 V617F mutation in myeloproliferative disordersInvestigation of JAK2 inhibition effectsGenomic and transcriptomic analysis of AMLUnderstanding molecular mechanisms of leukemogenesis

Key Characteristics

JAK2 V617F mutationDerived from MPD/MDS patientUsed in drug sensitivity studies
Generated on 6/17/2025

Basic Information

Database IDCVCL_1619
SpeciesHomo sapiens (Human)
Tissue SourcePeripheral blood[UBERON:UBERON_0000178]

Donor Information

Age65
Age CategoryAdult
SexMale

Disease Information

DiseaseAcute myeloid leukemia
LineageMyeloid
SubtypeAcute Myeloid Leukemia
OncoTree CodeAML

DepMap Information

Source TypeDSMZ
Source IDACH-000113_source

Known Sequence Variations

TypeGene/ProteinDescriptionZygosityNoteSource
Gene fusionAFDNKMT2A-AFDN, MLL-MLLT4, MLL-AF6--PubMed=15951289, PubMed=15921626

Haplotype Information (STR Profile)

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

Amelogenin
X,Y
CSF1PO
10,12
D13S317
11,12
D16S539
12,13
D18S51
14
D19S433
13,14
D21S11
29
D2S1338
23,25
D3S1358
16
D5S818
12
D7S820
12
D8S1179
12,15
FGA
19,24
Penta D
12
Penta E
12,14
TH01
6,9.3
TPOX
11
vWA
14,17
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

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).

Next-generation characterization of the Cancer Cell Line Encyclopedia.

Sellers W.R.

Nature 569:503-508(2019).

Prioritization of cancer therapeutic targets using CRISPR-Cas9 screens.

Stronach E.A., Saez-Rodriguez J., Yusa K., Garnett M.J.

Nature 568:511-516(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).

Parallel genome-scale loss of function screens in 216 cancer cell lines for the identification of context-specific genetic dependencies.

Golub T.R., Root D.E., Hahn W.C.

Sci. Data 1:140035-140035(2014).

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).

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).

Expression of a retinoic acid receptor gene in myeloid leukemia cells.

Wang C., Curtis J.E., Minden M.D., McCulloch E.A.

Leukemia 3:264-269(1989).

The leukemia-lymphoma cell line factsbook.";

Drexler H.G.

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