DMS 114Homo sapiens (Human)Cancer cell line

Also known as: Darmouth Medical School 114, DMS114, DMS-114

🤖 AI SummaryBased on 11 publications

DMS114

Quick Overview

Human small cell lung cancer cell line with known genetic alterations.

Detailed Summary

DMS114 is a human small cell lung cancer (SCLC) cell line derived from a patient with lung cancer. It is commonly used in research to study the molecular mechanisms of SCLC, including the role of specific genes and pathways in tumor progression and drug resistance. The cell line has been characterized in multiple studies for its genetic and phenotypic features, including mutations in the PARD3 gene and alterations in cell polarity complexes. DMS114 is also utilized in investigations related to DNA repair mechanisms and the response to chemotherapeutic agents, such as etoposide and PARP inhibitors. Its utility in understanding the genetic basis of cancer and developing targeted therapies makes it a valuable resource in oncology research.

Research Applications

Molecular mechanisms of SCLCGenetic alterations in cancerDNA repair mechanismsDrug resistance in cancerTargeted therapy development

Key Characteristics

Mutations in PARD3 geneAlterations in cell polarity complexesResponse to chemotherapeutic agentsUtilized in studies of DNA repair pathways
Generated on 6/16/2025

Basic Information

Database IDCVCL_1174
SpeciesHomo sapiens (Human)
Tissue SourceLung[UBERON:UBERON_0002048]

Donor Information

Age68
Age CategoryAdult
SexMale
Racecaucasian

Disease Information

DiseaseThoracic SMARCA4-deficient undifferentiated tumor
LineageLung
SubtypeSMARCA4-deficient undifferentiated tumor

DepMap Information

Source TypeATCC
Source IDACH-000530_source

Known Sequence Variations

TypeGene/ProteinDescriptionZygosityNoteSource
MutationSimpleTP53p.Arg213Ter (c.637C>T)Unspecified-Unknown
MutationUnexplicitPARD3BEx2-14delHomozygous-PubMed=20215515
MutationSimpleSMARCA4p.Glu1310Ter (c.3928G>T)Homozygous-Unknown

Haplotype Information (STR Profile)

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

Amelogenin
X
CSF1PO
10,11
D13S317
13
D16S539
12
D18S51
18
D19S433
13
D21S11
29
D2S1338
17
D3S1358
14,17
D5S818
12
D7S820
10,11
D8S1179
12,13
FGA
21
Penta D
11,13
Penta E
7,13
TH01
8,9.3
TPOX
8,11
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

Molecular and pathologic characterization of YAP1-expressing small cell lung cancer cell lines leads to reclassification as SMARCA4-deficient malignancies.

Burr M.L., Sutherland K.D.

Clin. Cancer Res. 30:1846-1858(2024).

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).

A landscape of pharmacogenomic interactions in cancer.";

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

Cell 166:740-754(2016).

Proteomic profiling identifies dysregulated pathways in small cell lung cancer and novel therapeutic targets including PARP1.

Heymach J.V.

Cancer Discov. 2:798-811(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).

JFCR39, a panel of 39 human cancer cell lines, and its application in the discovery and development of anticancer drugs.

Kong D.-X., Yamori T.

Bioorg. Med. Chem. 20:1947-1951(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).

p53-defective tumors with a functional apoptosome-mediated pathway: a new therapeutic target.

Tomoda H., Yamori T., Tsuruo T.

J. Natl. Cancer Inst. 97:765-777(2005).

The role of RAD51 in etoposide (VP16) resistance in small cell lung cancer.

Hansen L.T., Lundin C., Spang-Thomsen M., Petersen L.N., Helleday T.

Int. J. Cancer 105:472-479(2003).

In vitro invasion of small-cell lung cancer cell lines correlates with expression of epidermal growth factor receptor.

Poulsen H.S.

Br. J. Cancer 78:631-640(1998).

Cellular radiosensitivity of small-cell lung cancer cell lines.";

Krarup M., Poulsen H.S., Spang-Thomsen M.

Int. J. Radiat. Oncol. Biol. Phys. 38:191-196(1997).

Resistance mechanisms determining the in vitro sensitivity to paclitaxel of tumour cells cultured from patients with ovarian cancer.

van Zijl P.L.

Eur. J. Cancer 31A:230-237(1995).

Isolation and growth characteristics of continuous cell lines from small-cell carcinoma of the lung.

Noll W.W., Cate C.C., Maurer L.H.

Cancer 45:906-918(1980).

Feasibility of drug screening with panels of human tumor cell lines using a microculture tetrazolium assay.

Fine D.L., Abbott B.J., Mayo J.G., Shoemaker R.H., Boyd M.R.

Cancer Res. 48:589-601(1988).

Growth characteristics and heterogeneity of small cell carcinoma of the lung.

Vindelov L.L., Hansen H.H., Spang-Thomsen M.

Recent Results Cancer Res. 97:47-54(1985).

Metabolic activation of 4-ipomeanol in human lung, primary pulmonary carcinomas, and established human pulmonary carcinoma cell lines.

Adelberg S., Czerwinski M.J., McMahon N.A., Eggleston J.C., Boyd M.R.

J. Natl. Cancer Inst. 82:1420-1426(1990).

Feasibility of a high-flux anticancer drug screen using a diverse panel of cultured human tumor cell lines.

Gray-Goodrich M., Campbell H., Mayo J.G., Boyd M.R.

J. Natl. Cancer Inst. 83:757-766(1991).

Web Resources