SKNO-1Homo sapiens (Human)Cancer cell line

Also known as: SKNO1, Skno-1

🤖 AI SummaryBased on 9 publications

Quick Overview

SKNO-1 is a human myeloid leukemia cell line derived from a patient with t(8;21) and monosomy 17, used in leukemia research.

Detailed Summary

SKNO-1 is a human myeloid leukemia cell line established from the bone marrow of a 22-year-old male with acute myeloblastic leukemia (AML) M2. It carries the t(8;21) translocation and monosomy 17, which are associated with disease progression and resistance to therapy. The cell line is dependent on granulocyte-macrophage colony-stimulating factor (GM-CSF) for growth and exhibits overexpression of the p53 protein, which is linked to poor prognosis in leukemia. SKNO-1 is used in studies of leukemogenesis, molecular mechanisms of myeloid malignancies, and drug development for AML. It is also utilized in research on the role of p53 mutations in disease progression and in identifying therapeutic targets for leukemia treatment.

Research Applications

Leukemogenesis studiesMolecular mechanisms of myeloid malignanciesDrug development for AMLp53 mutation analysis in leukemia progression

Key Characteristics

t(8;21) translocationMonosomy 17GM-CSF-dependent growthOverexpression of p53 protein
Generated on 6/18/2025

Basic Information

Database IDCVCL_2196
SpeciesHomo sapiens (Human)
Tissue SourceBone marrow[UBERON:UBERON_0002371]

Donor Information

Age22
Age CategoryAdult
SexMale

Disease Information

DiseaseAcute myeloblastic leukemia with maturation
LineageMyeloid
SubtypeAML with Maturation
OncoTree CodeAM

DepMap Information

Source TypeDSMZ
Source IDACH-001656_source

Known Sequence Variations

TypeGene/ProteinDescriptionZygosityNoteSource
MutationSimpleTP53p.His368Arg (c.1103G>A)Homozygous-Unknown, PubMed=7772516
MutationSimpleTP53p.Arg248Gln (c.743G>A)UnspecifiedSomatic mutation acquired during proliferationPubMed=20575032
MutationSimpleKITp.Asn822Lys (c.2466T>A) (N818K)Unspecified-Wistar
Gene fusionRUNX1RUNX1-RUNX1T1, AML1-ETO--PubMed=15843827, PubMed=11753612

Haplotype Information (STR Profile)

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

Amelogenin
X
CSF1PO
12,13
D13S317
8,11
D16S539
10,11
D18S51
13,14
D19S433
13,15
D21S11
29,30
D2S1338
19
D3S1358
16
D5S818
10,13
D7S820
10,12
D8S1179
14,15
FGA
23
Penta D
9
Penta E
11,12
TH01
7
TPOX
8,9
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

The LL-100 panel: 100 cell lines for blood cancer studies.";

MacLeod R.A.F., Nagel S., Steube K.G., Uphoff C.C., Drexler H.G.

Sci. Rep. 9:8218-8218(2019).

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).

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).

Two cell lines of t(8;21) acute myeloid leukemia with activating KIT exon 17 mutation: models for the 'second hit' hypothesis.

Schwabe M., Lubbert M.

Leukemia 22:1792-1794(2008).

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

Fioretos T.

Leukemia 19:1042-1050(2005).

Molecular characterization of genomic AML1-ETO fusions in childhood leukemia.

Dicks B.M., Wiencke J.K., Wiemels J.L.

Leukemia 15:1906-1913(2001).

p53 alterations in human leukemia-lymphoma cell lines: in vitro artifact or prerequisite for cell immortalization?

Uphoff C.C.

Leukemia 14:198-206(2000).

Expression of the TCL1 gene at 14q32 in B-cell malignancies but not in adult T-cell leukemia.

Aizawa Y., Ueda R., Seto M.

Jpn. J. Cancer Res. 89:712-718(1998).

Establishment of a myeloid leukaemic cell line (SKNO-1) from a patient with t(8;21) who acquired monosomy 17 during disease progression.

Murayama T., Koizumi T., Nishimura R., Isobe T., Chihara K.

Br. J. Haematol. 89:805-811(1995).

The leukemia-lymphoma cell line factsbook.";

Drexler H.G.

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