MDA-MB-453Homo sapiens (Human)Cancer cell line

Also known as: MDA-MB 453, MDA MB 453, MDA-MB453, MDAMB453, MDA-453, MDA453, MD Anderson-Metastatic Breast-453, MDA-MB-345

🤖 AI SummaryBased on 13 publications

Quick Overview

Human breast cancer cell line with known genetic and molecular characteristics.

Detailed Summary

MDA-MB-453 is a human breast cancer cell line derived from a metastatic site, specifically a pleural effusion. It is widely used in cancer research for studying tumor biology, drug sensitivity, and genetic alterations. The cell line exhibits specific molecular features, including overexpression of certain genes and distinct chromosomal abnormalities, which make it a valuable model for investigating breast cancer mechanisms and therapeutic responses. Its use in various studies highlights its relevance in understanding cancer progression and developing targeted therapies.

Research Applications

Cancer biologyDrug screeningGenetic and molecular studiesTumor progression analysis

Key Characteristics

Metastatic originGenetic instabilityOverexpression of specific genesDistinct chromosomal abnormalities
Generated on 6/15/2025

Basic Information

Database IDCVCL_0418
SpeciesHomo sapiens (Human)
Tissue SourcePericardial effusion[UBERON:UBERON_0002409]

Donor Information

Age48
Age CategoryAdult
SexFemale
Racecaucasian
Subtype FeaturesHER2+

Disease Information

DiseaseBreast adenocarcinoma
LineageBreast
SubtypeInvasive Breast Carcinoma
OncoTree CodeBRCA

DepMap Information

Source TypeATCC
Source IDACH-000910_source

Known Sequence Variations

TypeGene/ProteinDescriptionZygosityNoteSource
MutationSimpleARp.Gln868His (c.2604G>T)Unspecified-from parent cell line MDA-MB-453
MutationSimpleCDH1p.Trp638Ter (c.1913G>A)Homozygous-from parent cell line MDA-MB-453
MutationSimpleKRASp.Gly13Asp (c.38G>A)HeterozygousSomaticfrom parent cell line MDA-MB-231
MutationSimplePIK3CAp.His1047Arg (c.3140A>G)Unspecified-PubMed=25926053, PubMed=20570890
MutationSimplePTENp.Glu307Lys (c.919G>A)Heterozygous-from parent cell line MDA-MB-453
MutationUnexplicitTP53Ex10-11delHomozygous-from parent cell line MDA-MB-453

Haplotype Information (STR Profile)

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

Amelogenin
X
CSF1PO
10,12
D10S1248
14,15
D12S391
18,21
D13S317
12
D16S539
9
D18S51
15,20
D19S433
13,14
D1S1656
16.3,17.3
D21S11
29,31
D22S1045
15,16
D2S1338
23,24
D2S441
10
D3S1358
15
D5S818
11
D7S820
10
D8S1179
10,12
FGA
18,23
Penta D
9,10
Penta E
11
TH01
6
TPOX
10
vWA
17,18
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

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).

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).

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).

Genetic ancestry analysis reveals misclassification of commonly used cancer cell lines.

Mitra R., Nonn L., Kimbro K.S., Kittles R.A.

Cancer Epidemiol. Biomarkers Prev. 28:1003-1009(2019).

Multidimensional phenotyping of breast cancer cell lines to guide preclinical research.

Lakhani S.R.

Breast Cancer Res. Treat. 167:289-301(2018).

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).

Metabolic profiling of breast cancer: differences in central metabolism between subtypes of breast cancer cell lines.

Kammerer B.

J. Chromatogr. B 1000:95-104(2015).

Cell lines from human breast.";

Leibovitz A.

(In book chapter) Atlas of human tumor cell lines; Hay R.J., Park J.-G., Gazdar A.F. (eds.); pp.161-184; Academic Press; New York; USA (1994).

Breast cancer stem cells: tumourspheres and implications for therapy.";

Morrison B.J.

Thesis PhD (2010); Griffith University; Brisbane; Australia.

Long-term human breast carcinoma cell lines of metastatic origin: preliminary characterization.

Cailleau R.M., Olive M., Cruciger Q.V.J.

In Vitro 14:911-915(1978).

Mutations in p53 as potential molecular markers for human breast cancer.

Runnebaum I.B., Nagarajan M., Bowman M., Soto D., Sukumar S.

Proc. Natl. Acad. Sci. U.S.A. 88:10657-10661(1991).

Human tumor lines for cancer research.";

Fogh J.

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

Lack of relationship between CDK activity and G1 cyclin expression in breast cancer cells.

Sweeney K.J., Swarbrick A., Sutherland R.L., Musgrove E.A.

Oncogene 16:2865-2878(1998).

Altered gene expression in drug-resistant human breast cancer cells.

Wosikowski K., Schuurhuis D.H., Kops G.J.P.L., Saceda M., Bates S.E.

Clin. Cancer Res. 3:2405-2414(1997).

Comparative genomic hybridization analysis of 38 breast cancer cell lines: a basis for interpreting complementary DNA microarray data.

Gooden G.C., Ethier S.P., Kallioniemi A.H., Kallioniemi O.-P.

Cancer Res. 60:4519-4525(2000).

Assembly of microarrays for genome-wide measurement of DNA copy number.

Pinkel D., Albertson D.G.

Nat. Genet. 29:263-264(2001).

A formalin-fixed, paraffin-processed cell line standard for quality control of immunohistochemical assay of HER-2/neu expression in breast cancer.

Dodson A.R., Navabi H., Miller K.D., Balaton A.J.

Am. J. Clin. Pathol. 117:81-89(2002).

Reciprocal translocations in breast tumor cell lines: cloning of a t(3;20) that targets the FHIT gene.

Birnbaum D., Chaffanet M.

Genes Chromosomes Cancer 35:204-218(2002).

A recurrent chromosome translocation breakpoint in breast and pancreatic cancer cell lines targets the neuregulin/NRG1 gene.

Edwards P.A.W., Chaffanet M.

Genes Chromosomes Cancer 37:333-345(2003).

Molecular characterization of breast cancer cell lines by a low-density microarray.

Remacle J.

Int. J. Oncol. 27:881-892(2005).

BRCA1 mutation analysis of 41 human breast cancer cell lines reveals three new deleterious mutants.

van den Ouweland A.M.W., Merajver S.D., Ethier S.P., Schutte M.

Cancer Res. 66:41-45(2006).

Thirteen new p53 gene mutants identified among 41 human breast cancer cell lines.

Wasielewski M., Elstrodt F., Klijn J.G.M., Berns E.M.J.J., Schutte M.

Breast Cancer Res. Treat. 99:97-101(2006).

A collection of breast cancer cell lines for the study of functionally distinct cancer subtypes.

Johnson M.D., Lippman M.E., Ethier S.P., Gazdar A.F., Gray J.W.

Cancer Cell 10:515-527(2006).

The morphologies of breast cancer cell lines in three-dimensional assays correlate with their profiles of gene expression.

Petersen O.W., Gray J.W., Bissell M.J.

Mol. Oncol. 1:84-96(2007).

Molecular profiling of breast cancer cell lines defines relevant tumor models and provides a resource for cancer gene discovery.

Pollack J.R.

PLoS ONE 4:E6146-E6146(2009).

Distinct gene mutation profiles among luminal-type and basal-type breast cancer cell lines.

den Bakker M.A., Foekens J.A., Martens J.W.M., Schutte M.

Breast Cancer Res. Treat. 121:53-64(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).

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).

Reassessment of estrogen receptor expression in human breast cancer cell lines.

Ford C.H.J., Al-Bader M., Al-Ayadhi B., Francis I.

Anticancer Res. 31:521-527(2011).

Update on the molecular profile of the MDA-MB-453 cell line as a model for apocrine breast carcinoma studies.

Vranic S., Gatalica Z., Wang Z.-Y.

Oncol. Lett. 2:1131-1137(2011).

Proteomic portrait of human breast cancer progression identifies novel prognostic markers.

Geiger T., Madden S.F., Gallagher W.M., Cox J., Mann M.

Cancer Res. 72:2428-2439(2012).

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).

Essential gene profiles in breast, pancreatic, and ovarian cancer cells.

Rottapel R., Neel B.G., Moffat J.

Cancer Discov. 2:172-189(2012).

An androgen receptor mutation in the MDA-MB-453 cell line model of molecular apocrine breast cancer compromises receptor activity.

Hanson A.R., Birrell S.N., Butler L.M., Hickey T.E., Tilley W.D.

Endocr. Relat. Cancer 19:599-613(2012).

miRNA expression profiling of 51 human breast cancer cell lines reveals subtype and driver mutation-specific miRNAs.

Martens J.W.M.

Breast Cancer Res. 15:R33.1-R33.17(2013).

Glutamine sensitivity analysis identifies the xCT antiporter as a common triple-negative breast tumor therapeutic target.

McCormick F., Gray J.W.

Cancer Cell 24:450-465(2013).

Modeling precision treatment of breast cancer.";

Collisson E.A., van 't Veer L.J., Spellman P.T., Gray J.W.

Genome Biol. 14:R110.1-R110.14(2013).

A comprehensive transcriptional portrait of human cancer cell lines.

Settleman J., Seshagiri S., Zhang Z.-M.

Nat. Biotechnol. 33:306-312(2015).

A resource for cell line authentication, annotation and quality control.

Neve R.M.

Nature 520:307-311(2015).

The proteomic landscape of triple-negative breast cancer.";

Irie H.Y., Lee S.-I., Blau C.A., Villen J.

Cell Rep. 11:630-644(2015).