SW626Homo sapiens (Human)Cancer cell line

Also known as: SW 626, SW-626, SWS-26

🤖 AI SummaryBased on 14 publications

Quick Overview

SW626 is a human ovarian cancer cell line used in cancer research.

Detailed Summary

SW626 is a human ovarian cancer cell line that has been extensively studied in cancer research. It is known for its ability to form tumors in nude mice, which makes it a valuable model for studying ovarian cancer. The cell line has been used to investigate various aspects of cancer biology, including mutations in the BRCA1 and BRCA2 genes, as well as the role of the Wnt/β-catenin signaling pathway. SW626 has also been used to study the effects of genetic alterations on tumor development and response to therapies. Research on SW626 has contributed to understanding the molecular mechanisms underlying ovarian cancer progression and has provided insights into potential therapeutic targets.

Research Applications

Cancer researchTumor formation in nude miceBRCA1/BRCA2 mutation analysisWnt/β-catenin signaling pathway studiesTherapeutic target identification

Key Characteristics

Tumor formation in vivoBRCA1/BRCA2 mutationsWnt/β-catenin pathway activationResponse to therapeutic agents
Generated on 6/17/2025

Basic Information

Database IDCVCL_1725
SpeciesHomo sapiens (Human)
Tissue SourceOvary[UBERON:UBERON_0000992]

Donor Information

Age46
Age CategoryAdult
SexFemale

Disease Information

DiseaseColon adenocarcinoma
LineageBowel
SubtypeColon Adenocarcinoma
OncoTree CodeCOAD

DepMap Information

Source TypeATCC
Source IDACH-001399_source

Known Sequence Variations

TypeGene/ProteinDescriptionZygosityNoteSource
MutationSimpleTP53p.Gly262Val (c.785G>T)Homozygous-Unknown, Unknown
MutationSimpleSMAD4p.Asp351His (c.1051G>C)Homozygous-from parent cell line Caco-2
MutationSimpleKRASp.Gly12Val (c.35G>T)HeterozygousAcquiredUnknown, Unknown
MutationSimpleAPCp.Arg976fs*9 (c.2926_2927insA)Homozygous-Unknown, Unknown, Unknown

Haplotype Information (STR Profile)

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

Amelogenin
X
CSF1PO
11
D13S317
11
D16S539
11
D18S51
14
D19S433
14
D21S11
27,29
D2S1338
25
D3S1358
15,17
D5S818
12
D7S820
10,12
D8S1179
11
FGA
21,23
Penta D
9,13
Penta E
7,11
TH01
9.3
TPOX
8
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

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).

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).

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).

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

Neve R.M.

Nature 520:307-311(2015).

Profiling of actionable gene alterations in ovarian cancer by targeted deep sequencing.

Ichikawa H., Shibata T., Yokota J., Okamoto A., Kohno T.

Int. J. Oncol. 46:2389-2398(2015).

BRCA1/2 mutation analysis in 41 ovarian cell lines reveals only one functionally deleterious BRCA1 mutation.

Mills G.B., Hennessy B.T.

Mol. Oncol. 7:567-579(2013).

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).

FGFR2 mutations are rare across histologic subtypes of ovarian cancer.

Campbell I.G., Pollock P.M.

Gynecol. Oncol. 117:125-129(2010).

Mutations of the BRAF gene in human cancer.";

Marshall C.J., Wooster R., Stratton M.R., Futreal P.A.

Nature 417:949-954(2002).

Searching for microsatellite mutations in coding regions in lung, breast, ovarian and colorectal cancers.

Minna J.D.

Oncogene 20:1005-1009(2001).

Evidence for the colonic origin of ovarian cancer cell line SW626.";

Furlong M.T., Hough C.D., Sherman-Baust C.A., Pizer E.S., Morin P.J.

J. Natl. Cancer Inst. 91:1327-1328(1999).

Mutation of the PTEN tumor suppressor gene is not a feature of ovarian cancers.

Berchuck A., Futreal P.A.

Gynecol. Oncol. 70:13-16(1998).

Cell surface antigens of human ovarian and endometrial carcinoma defined by mouse monoclonal antibodies.

Mattes M.J., Cordon-Cardo C., Lewis J.L. Jr., Old L.J., Lloyd K.O.

Proc. Natl. Acad. Sci. U.S.A. 81:568-572(1984).

Polymorphic enzyme analysis of cultured human tumor cell lines.";

Dracopoli N.C., Fogh J.

J. Natl. Cancer Inst. 70:469-476(1983).

Human tumor lines for cancer research.";

Fogh J.

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

Absence of HeLa cell contamination in 169 cell lines derived from human tumors.

Fogh J., Wright W.C., Loveless J.D.

J. Natl. Cancer Inst. 58:209-214(1977).

One hundred and twenty-seven cultured human tumor cell lines producing tumors in nude mice.

Fogh J., Fogh J.M., Orfeo T.

J. Natl. Cancer Inst. 59:221-226(1977).

Web Resources