SK-MEL-30Homo sapiens (Human)Cancer cell line
Also known as: AW-Mel, SKMEL30, Sk Mel30, SKMEL-30, SK Mel 30, SK-Mel-30
Quick Overview
Human melanoma cell line with BRAF V600E mutation and PTEN loss.
Detailed Summary
Research Applications
Key Characteristics
Basic Information
Database ID | CVCL_0039 |
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Species | Homo sapiens (Human) |
Donor Information
Age | 67 |
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Age Category | Adult |
Sex | Male |
Race | caucasian |
Disease Information
Disease | Cutaneous melanoma |
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Lineage | Skin |
Subtype | Cutaneous Melanoma |
OncoTree Code | SKCM |
DepMap Information
Source Type | DSMZ |
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Source ID | ACH-000810_source |
Known Sequence Variations
Type | Gene/Protein | Description | Zygosity | Note | Source |
---|---|---|---|---|---|
MutationSimple | TP53 | p.Thr284Argfs*21 (c.851_852delCA) (p.R283fs, c.849_850del2) | Heterozygous | - | Unknown, Unknown |
MutationSimple | TERT | c.1-124C>T (c.228C>T) (C228T) | Unspecified | In promoter | from parent cell line Hep-G2 |
MutationSimple | NRAS | p.Gln61Lys (c.181C>A) | Unspecified | Acquired during resistance selection process | PubMed=26214590 |
MutationSimple | CDKN2A | p.Pro114Leu (c.341C>T) (p.Ala128Ala, c.384C>T) | Homozygous | - | Unknown, Unknown, PubMed=9598804 |
MutationSimple | APC | p.Gln1406Ter (c.4216C>T) | Heterozygous | - | Unknown, Unknown |
MutationSimple | APC | p.Gly1339Arg (c.4015G>C) | Heterozygous | - | Unknown, Unknown |
Gene deletion | CDKN2B | - | Homozygous | - | PubMed=35933914 |
Haplotype Information (STR Profile)
Short Tandem Repeat (STR) profile for cell line authentication.
Loading gene expression data...
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).
Quantitative proteomics of the Cancer Cell Line Encyclopedia.";
Sellers W.R., Gygi S.P.
Cell 180:387-402.e16(2020).
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).
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).
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).
Genetic interaction between NRAS and BRAF mutations and PTEN/MMAC1 inactivation in melanoma.
Tsao H., Goel V., Wu H., Yang G., Haluska F.G.
J. Invest. Dermatol. 122:337-341(2004).
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).
Relative reciprocity of NRAS and PTEN/MMAC1 alterations in cutaneous melanoma cell lines.
Tsao H., Zhang X., Fowlkes K., Haluska F.G.
Cancer Res. 60:1800-1804(2000).
Virtually 100% of melanoma cell lines harbor alterations at the DNA level within CDKN2A, CDKN2B, or one of their downstream targets.
Fountain J.W.
Genes Chromosomes Cancer 22:157-163(1998).
Production and characterization of antibodies against human tyrosinase.
Bouchard B., Vijayasaradhi S., Houghton A.N.
J. Invest. Dermatol. 102:291-295(1994).
Surface antigens of melanocytes and melanomas. Markers of melanocyte differentiation and melanoma subsets.
Houghton A.N., Eisinger M., Albino A.P., Cairncross J.G., Old L.J.
J. Exp. Med. 156:1755-1766(1982).
Serological survey of normal humans for natural antibody to cell surface antigens of melanoma.
Old L.J.
Proc. Natl. Acad. Sci. U.S.A. 77:4260-4264(1980).
Detection of cell surface and intracellular antigens by human monoclonal antibodies. Hybrid cell lines derived from lymphocytes of patients with malignant melanoma.
Old L.J.
J. Exp. Med. 158:53-65(1983).
Monoclonal antibody to an intracellular antigen images human melanoma transplants in nu/nu mice.
Zanzonico P.B., Bigler R.E., Yeh S., Oettgen H.F., Old L.J.
Proc. Natl. Acad. Sci. U.S.A. 84:4200-4204(1987).
A molecular mechanism of complement resistance of human melanoma cells.
Panneerselvam M., Welt S., Old L.J., Vogel C.-W.
J. Immunol. 136:2534-2541(1986).
Induction of growth factor RNA expression in human malignant melanoma: markers of transformation.
Albino A.P., Davis B.M., Nanus D.M.
Cancer Res. 51:4815-4820(1991).
Cell surface antigens of human malignant melanoma: mixed hemadsorption assays for humoral immunity to cultured autologous melanoma cells.
Old L.J.
Proc. Natl. Acad. Sci. U.S.A. 73:3278-3282(1976).
Cell surface antigens of human malignant melanoma. II. Serological typing with immune adherence assays and definition of two new surface antigens.
Shiku H., Takahashi T., Oettgen H.F., Old L.J.
J. Exp. Med. 144:873-881(1976).
Malignant melanoma. Current status of the search for melanoma-specific antigens.
Houghton A.N., Oettgen H.F., Old L.J.
(In book chapter) Immunodermatology. Comprehensive Immunology, Vol 7; Safai B., Good R.A. (eds.); pp.557-576; Springer; Boston; USA (1981).