SUM190PTHomo sapiens (Human)Cancer cell line

Also known as: 190PT, SUM190, SUM 190, SUM-190, SUM 190PT, SUM-190PT

🤖 AI SummaryBased on 14 publications

Quick Overview

SUM190PT is a breast cancer cell line derived from inflammatory breast cancer, used for studying tumor biology and drug develop...

Detailed Summary

SUM190PT is a breast cancer cell line established from an invasive ductal carcinoma of the breast, specifically classified as inflammatory breast cancer. It is widely used in research to study the molecular mechanisms of breast cancer progression and metastasis. This cell line exhibits characteristics of basal-like and luminal subtypes, making it a valuable model for understanding the heterogeneity of breast cancer. SUM190PT is known for its ability to form tumor xenografts in immunocompromised mice, facilitating in vivo studies of tumor growth and response to therapies. The cell line has been utilized in studies involving genomic profiling, drug sensitivity testing, and investigation of signaling pathways such as PI3K/AKT and MAPK. Its genetic and molecular profiles provide insights into the complexities of breast cancer, aiding in the development of targeted therapies.

Research Applications

Cancer biology researchDrug developmentGenomic profilingTumor metastasis studiesSignaling pathway analysis

Key Characteristics

Inflammatory breast cancer modelBasal-like and luminal subtype characteristicsTumor xenograft formationPI3K/AKT pathway activationGenomic instability
Generated on 6/20/2025

Basic Information

Database IDCVCL_3423
SpeciesHomo sapiens (Human)
Tissue SourceBreast[UBERON:UBERON_0000310]

Donor Information

Age CategoryUnknown
SexFemale
Subtype Featuresbasal_A HER2+

Disease Information

DiseaseBreast inflammatory carcinoma
LineageBreast
SubtypeInvasive Breast Carcinoma
OncoTree CodeBRCA

DepMap Information

Source TypeAsterand
Source IDACH-001393_source

Known Sequence Variations

TypeGene/ProteinDescriptionZygosityNoteSource
MutationSimpleTP53p.Gln317Ter (c.949C>T)Unspecified-PubMed=16541312
MutationSimplePIK3CAp.His1047Arg (c.3140A>G)Unspecified-PubMed=25926053, PubMed=20570890

Haplotype Information (STR Profile)

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

Amelogenin
X
CSF1PO
8,10
D13S317
11,12
D16S539
11
D18S51
12
D21S11
28,30
D3S1358
15
D5S818
11,12
D7S820
8,11
D8S1179
10,15
FGA
22
Penta D
10,11
Penta E
18,19
TH01
9
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

Comparative transcriptional analyses of preclinical models and patient samples reveal MYC and RELA driven expression patterns that define the molecular landscape of IBC.

Viens P., Birnbaum D., Devi G.R., Cristofanilli M., Van Laere S.

NPJ Breast Cancer 8:12.1-12.12(2022).

Development and implementation of the SUM breast cancer cell line functional genomics knowledge base.

Duchinski K., Couch D., Gray J.W., Kappler C.S.

NPJ Breast Cancer 6:30.1-30.14(2020).

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

Liang H.

Cancer Cell 31:225-239(2017).

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

Neve R.M.

Nature 520:307-311(2015).

Characterization of cell lines derived from breast cancers and normal mammary tissues for the study of the intrinsic molecular subtypes.

Harrell J.C., Roman E., Adamo B., Troester M.A., Perou C.M.

Breast Cancer Res. Treat. 142:237-255(2013).

Inflammatory breast cancer (IBC): clues for targeted therapies.";

Cristofanilli M.

Breast Cancer Res. Treat. 140:23-33(2013).

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).

Phenotypic and molecular characterization of MCF10DCIS and SUM breast cancer cell lines.

Barnabas N., Cohen D.

Int. J. Breast Cancer 2013:872743.1-872743.16(2013).

Molecular characterisation of cell line models for triple-negative breast cancers.

Reis-Filho J.S., Tutt A.

BMC Genomics 13:619.1-619.14(2012).

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).

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).

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).

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).

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).

Evidence that both genetic instability and selection contribute to the accumulation of chromosome alterations in cancer.

Edwards P.A.W., Caldas C.

Carcinogenesis 26:923-930(2005).

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).

Molecular cytogenetic analysis of 11 new breast cancer cell lines.";

Kallioniemi O.-P., Ethier S.P.

Br. J. Cancer 81:1328-1334(1999).

Constitutive activation of pp125fak in newly isolated human breast cancer cell lines.

Ignatoski K.M.W., Ethier S.P.

Breast Cancer Res. Treat. 54:173-182(1999).

Genomic profiling of pre-clinical models of inflammatory breast cancer identifies a signature of epithelial plasticity and suppression of TGFbeta signaling.

Wu H., Zook M.B., Barsky S.H., Krishnamurthy S., Cristofanilli M.

J. Clin. Exp. Pathol. 2:119.1-119.11(2012).