SK-MEL-1Homo sapiens (Human)Cancer cell line

Also known as: SK 1, SKMEL1, SkMEL-1, SKMEL-1, SK-Mel1, SK-Mel 1, SK Mel 1, SK-Mel-1

🤖 AI SummaryBased on 15 publications

Quick Overview

Human melanoma cell line with BRAF V600E mutation, used in cancer research.

Detailed Summary

SK-MEL-1 is a human melanoma cell line derived from a malignant melanoma. It is characterized by the presence of the BRAF V600E mutation, which is a common driver mutation in melanoma. This cell line is widely used in research to study the mechanisms of melanoma progression and to test the efficacy of targeted therapies, particularly those directed against the MAPK pathway. The cell line has been utilized in studies investigating the role of NF1 loss and its association with RAS activation and MEK dependence. Additionally, SK-MEL-1 has been employed in studies examining the impact of PTEN and RB1 tumor suppressor inactivation on RAF dependence in BRAF-mutant melanomas. The cell line is also part of large-scale genomic and transcriptomic studies, contributing to the understanding of cancer cell line diversity and the development of predictive models for drug response.

Research Applications

BRAF V600E mutation studiesMAPK pathway researchNF1 loss and RAS activationPTEN and RB1 inactivation studiesDrug response prediction models

Key Characteristics

BRAF V600E mutationNF1 lossPTEN and RB1 inactivationMEK dependence
Generated on 6/14/2025

Basic Information

Database IDCVCL_0068
SpeciesHomo sapiens (Human)
Tissue SourceThoracic lymph duct[UBERON:UBERON_0007644]

Donor Information

Age29
Age CategoryAdult
SexMale
Racecaucasian

Disease Information

DiseaseMelanoma
LineageSkin
SubtypeMelanoma
OncoTree CodeMEL

DepMap Information

Source TypeATCC
Source IDACH-000465_source

Known Sequence Variations

TypeGene/ProteinDescriptionZygosityNoteSource
MutationSimpleCTNNB1p.Ser33Cys (c.98C>G)Heterozygous-Unknown, Unknown, Unknown
MutationSimpleBRAFp.Val600Glu (c.1799T>A)Unspecified-PubMed=26214590

Haplotype Information (STR Profile)

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

Amelogenin
X,Y
CSF1PO
12,13
D13S317
11
D16S539
11,12
D18S51
13,16
D19S433
15
D21S11
29,32.2
D2S1338
19,23
D3S1358
14,16
D5S818
12,13
D7S820
12
D8S1179
13,16
FGA
17,20
Penta D
11,13
Penta E
7,21
TH01
6
TPOX
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

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).

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).

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

Liang H.

Cancer Cell 31:225-239(2017).

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).

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 NF1 in cutaneous melanoma is associated with RAS activation and MEK dependence.

Rosen N., Solit D.B.

Cancer Res. 74:2340-2350(2014).

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).

Concurrent loss of the PTEN and RB1 tumor suppressors attenuates RAF dependence in melanomas harboring (V600E)BRAF.

Wolchok J.D., Houghton A.N., Solit D.B.

Oncogene 31:446-457(2012).

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).

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).

Immunocytochemical analysis of cell lines derived from solid tumors.

Quentmeier H., Osborn M., Reinhardt J., Zaborski M., Drexler H.G.

J. Histochem. Cytochem. 49:1369-1378(2001).

Expression of hyaluronidase by tumor cells induces angiogenesis in vivo.

Markowitz S.D., Willson J.K.V., Sy M.-S.

Proc. Natl. Acad. Sci. U.S.A. 93:7832-7837(1996).

Surface antigens of human melanoma cells defined by monoclonal antibodies. I. Biochemical characterization of two antigens found on cell lines and fresh tumors of diverse tissue origin.

Johnson J.P., Demmer-Dieckmann M., Meo T., Hadam M.R., Riethmuller G.

Eur. J. Immunol. 11:825-831(1981).

Polymorphic enzyme analysis of cultured human tumor cell lines.";

Dracopoli N.C., Fogh J.

J. Natl. Cancer Inst. 70:469-476(1983).

Suspension culture of a pigment-producing cell line derived from a human malignant melanoma.

Oettgen H.F., Aoki T., Old L.J., Boyse E.A., de Harven E., Mills G.M.

J. Natl. Cancer Inst. 41:827-843(1968).

Human tumor lines for cancer research.";

Fogh J.

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

Feasibility of drug screening with panels of human tumor cell lines using a microculture tetrazolium assay.

Fine D.L., Abbott B.J., Mayo J.G., Shoemaker R.H., Boyd M.R.

Cancer Res. 48:589-601(1988).

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).

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).