KYSE-410Homo sapiens (Human)Cancer cell line

Also known as: KYSE0410, Kyse410, KYSE410, KYSE 410

🤖 AI SummaryBased on 10 publications

Quick Overview

KYSE-410 is an esophageal squamous cell carcinoma cell line used in cancer research.

Detailed Summary

KYSE-410 is a human esophageal squamous cell carcinoma cell line derived from the KYSE series. It is widely used in research to study the molecular mechanisms of esophageal cancer, including gene expression, chromosomal abnormalities, and interactions with stromal cells. This cell line has been utilized in studies examining the role of hyaluronan in cancer progression and the effects of chemotherapeutic agents on tumor cell behavior. Additionally, KYSE-410 has been employed in investigations of genetic alterations, such as homozygous deletions and mutations in genes like LRP1B and PARD3, which are associated with cancer development and progression. The cell line's characteristics make it a valuable tool for understanding the genetic and molecular basis of esophageal squamous cell carcinoma.

Research Applications

Gene expression analysisChromosomal abnormality studiesCancer progression mechanismsDrug response profilingGenetic mutation analysis

Key Characteristics

Homozygous deletions in LRP1BExpression of PARD3Interaction with fibroblastsResponse to chemotherapeutic agents
Generated on 6/16/2025

Basic Information

Database IDCVCL_1352
SpeciesHomo sapiens (Human)
Tissue SourceEsophagus[UBERON:UBERON_0001043]

Donor Information

Age51
Age CategoryAdult
SexMale
Raceasian

Disease Information

DiseaseSquamous cell carcinoma of the esophagus
LineageEsophagus/Stomach
SubtypeEsophageal Squamous Cell Carcinoma
OncoTree CodeESCC

DepMap Information

Source TypeDSMZ
Source IDACH-000809_source

Known Sequence Variations

TypeGene/ProteinDescriptionZygosityNoteSource
MutationSimpleTP53p.Arg337Cys (c.1009C>T)Unspecified-PubMed=32321971
MutationSimpleKRASp.Gly12Cys (c.34G>T)Unspecified-PubMed=21173094

Haplotype Information (STR Profile)

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

Amelogenin
X
CSF1PO
12
D13S317
11
D16S539
10,12
D18S51
13,15
D19S433
13
D21S11
30
D2S1338
17,19
D3S1358
15,16
D5S818
13
D7S820
12
D8S1179
10
FGA
20
Penta D
11
Penta E
8,12
TH01
8
TPOX
8,11
vWA
16,18
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

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).

A landscape of pharmacogenomic interactions in cancer.";

Wessels L.F.A., Saez-Rodriguez J., McDermott U., Garnett M.J.

Cell 166:740-754(2016).

Esophageal squamous cell carcinoma cells modulate chemokine expression and hyaluronan synthesis in fibroblasts.

Grandoch M., Fischer J.W.

J. Biol. Chem. 291:4091-4106(2016).

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

Neve R.M.

Nature 520:307-311(2015).

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).

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).

Radiation sensitivities of 31 human oesophageal squamous cell carcinoma cell lines.

Shimada Y., Inazawa J., Imai T.

Int. J. Exp. Pathol. 86:231-240(2005).

Frequent silencing of low density lipoprotein receptor-related protein 1B (LRP1B) expression by genetic and epigenetic mechanisms in esophageal squamous cell carcinoma.

Imamura M., Amagasa T., Gray J.W., Hirohashi S., Inazawa J.

Cancer Res. 64:3741-3747(2004).

PUMA in head and neck cancer.";

Sidransky D.

Cancer Lett. 199:75-81(2003).

Gene expression profiling in human esophageal cancers using cDNA microarray.

Itami A., Yamasaki S., Imamura M.

Biochem. Biophys. Res. Commun. 286:792-801(2001).

Nonrandom chromosomal imbalances in esophageal squamous cell carcinoma cell lines: possible involvement of the ATF3 and CENPF genes in the 1q32 amplicon.

Yang Z.-Q., Imamura M., Nakamura Y., Amagasa T., Inazawa J.

Jpn. J. Cancer Res. 91:1126-1133(2000).

Multiple types of aberrations in the p16 (INK4a) and the p15(INK4b) genes in 30 esophageal squamous-cell-carcinoma cell lines.

Tanaka H., Shimada Y., Imamura M., Shibagaki I., Ishizaki K.

Int. J. Cancer 70:437-442(1997).

Analysis of gene amplification and overexpression in human esophageal-carcinoma cell lines.

Fukumoto M.

Int. J. Cancer 58:291-297(1994).

Characterization of 21 newly established esophageal cancer cell lines.

Shimada Y., Imamura M., Wagata T., Yamaguchi N., Tobe T.

Cancer 69:277-284(1992).