MM485Homo sapiens (Human)Cancer cell line

Also known as: MM 485

🤖 AI SummaryBased on 5 publications

Quick Overview

MM485 is a melanoma cell line with BRAF mutation and potential for research in melanoma therapies.

Detailed Summary

MM485 is a melanoma cell line derived from human tissue, characterized by a BRAF mutation. It has been used in studies to identify gene expression signatures associated with BRAF mutations, which are critical in melanoma development. Research on MM485 has contributed to understanding the molecular mechanisms of melanoma and the development of targeted therapies. The cell line is also involved in studies examining the relationship between UV exposure and p53 mutations, although no significant correlation was found in this specific cell line. MM485 is valuable for investigating the genetic and molecular changes in melanoma, particularly in the context of BRAF and p53 mutations, and their implications for treatment strategies.

Research Applications

BRAF mutation analysisGene expression profilingMelanoma therapy developmentp53 mutation studies

Key Characteristics

BRAF mutationPotential for targeted therapy research
Generated on 6/19/2025

Basic Information

Database IDCVCL_2610
SpeciesHomo sapiens (Human)
Tissue SourceLymph node[UBERON:UBERON_0000029]

Donor Information

Age CategoryUnknown
SexMale

Disease Information

DiseaseAmelanotic melanoma
LineageSkin
SubtypeMelanoma
OncoTree CodeMEL

DepMap Information

Source TypeCellBank Australia
Source IDACH-001973_source

Known Sequence Variations

TypeGene/ProteinDescriptionZygosityNoteSource
MutationSimpleNRASp.Gln61Arg (c.182A>G)Unspecified-PubMed=26214590
MutationSimpleCDKN2Ap.Trp100TerHomozygous-Unknown, PubMed=17363583, PubMed=9354451

Haplotype Information (STR Profile)

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

Amelogenin
X,Y
CSF1PO
11,12
D13S317
11,13
D16S539
11
D18S51
13,17
D19S433
12,14
D21S11
30
D2S1338
17,20
D3S1358
14
D5S818
11,12
D7S820
12
D8S1179
11,13
FGA
21,23
Penta D
10,12
Penta E
10,15
TH01
8
TPOX
9,10
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

Confirmation of a BRAF mutation-associated gene expression signature in melanoma.

Johansson P., Pavey S., Hayward N.K.

Pigment Cell Res. 20:216-221(2007).

Genome-wide loss of heterozygosity and copy number analysis in melanoma using high-density single-nucleotide polymorphism arrays.

Stark M.S., Hayward N.K.

Cancer Res. 67:2632-2642(2007).

Microarray expression profiling in melanoma reveals a BRAF mutation signature.

Meltzer P.S., Ringner M., Hayward N.K.

Oncogene 23:4060-4067(2004).

p53 mutations in human cutaneous melanoma correlate with sun exposure but are not always involved in melanomagenesis.

Zerp S.F., van Elsas A., Peltenburg L.T.C., Schrier P.I.

Br. J. Cancer 79:921-926(1999).

Constitutive transduction of peptide transporter and HLA genes restores antigen processing function and cytotoxic T cell-mediated immune recognition of human melanoma cells.

Coupar B., Qiu L., Parsons P.G., Moss D.J., Khanna R.

Int. J. Cancer 75:590-595(1998).

CDKN2A/p16 is inactivated in most melanoma cell lines.";

Gabrielli B.G., Parsons P.G., Hayward N.K.

Cancer Res. 57:4868-4875(1997).

Protein B61 as a new growth factor: expression of B61 and up-regulation of its receptor epithelial cell kinase during melanoma progression.

Toso R.J., Herlyn M., Bennett D.C.

Cancer Res. 55:2528-2532(1995).

Monoclonal antibody against human tyrosinase and reactive with melanotic and amelanotic melanoma cells.

McEwan M., Parsons P.G., Moss D.J.

J. Invest. Dermatol. 90:515-519(1988).

Gene expression in melanoma cell lines and cultured melanocytes: correlation between levels of c-src-1, c-myc and p53.

Chenevix-Trench G., Martin N.G., Ellem K.A.O.

Oncogene 5:1187-1193(1990).