NCI-H508Homo sapiens (Human)Cancer cell line

Also known as: H-508, H508, NCIH508, NCI H508

🤖 AI SummaryBased on 14 publications

Quick Overview

Human colorectal cancer cell line with KRAS and BRAF mutations.

Detailed Summary

The NCI-H508 cell line is a human colorectal cancer cell line derived from a colon tumor. It is characterized by specific genetic mutations in KRAS and BRAF, which are commonly associated with resistance to EGFR-targeted therapies. These mutations play a critical role in the development and progression of colorectal cancer, making NCI-H508 a valuable model for studying molecular mechanisms of drug resistance and for developing targeted therapeutic strategies. The cell line is also used in research to understand the genetic and epigenetic alterations that contribute to cancer heterogeneity and treatment outcomes.

Research Applications

Study of KRAS and BRAF mutations in colorectal cancerInvestigation of EGFR-targeted therapy resistanceMolecular mechanisms of cancer progressionDevelopment of targeted therapeutic strategies

Key Characteristics

KRAS mutationsBRAF mutationsResistance to EGFR inhibitorsModel for colorectal cancer research
Generated on 6/17/2025

Basic Information

Database IDCVCL_1564
SpeciesHomo sapiens (Human)
Tissue SourceAbdominal wall[UBERON:UBERON_0003697]

Donor Information

Age55
Age CategoryAdult
SexMale
Racecaucasian

Disease Information

DiseaseCecum adenocarcinoma
LineageBowel
SubtypeColon Adenocarcinoma
OncoTree CodeCOAD

DepMap Information

Source TypeATCC
Source IDACH-000360_source

Known Sequence Variations

TypeGene/ProteinDescriptionZygosityNoteSource
MutationSimpleTP53p.Arg273His (c.818G>A)Homozygous-Unknown, PubMed=16264262
MutationSimplePIK3CAp.Glu545Lys (c.1633G>A)Heterozygous-from parent cell line MCF-7
MutationSimpleBRAFp.Gly596Arg (c.1786G>C)Heterozygous-from parent cell line NCI-H508

Haplotype Information (STR Profile)

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

Amelogenin
X
CSF1PO
11,12
D13S317
8,12
D16S539
12
D18S51
18
D19S433
14
D21S11
29,32.2
D2S1338
18,19,27
D3S1358
14,17
D5S818
12
D7S820
8,12
D8S1179
12
FGA
24,25
Penta D
12
Penta E
10,12
TH01
9,9.3
TPOX
8,11
vWA
15,16
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).

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).

Genomic determinants of protein abundance variation in colorectal cancer cells.

Wessels L.F.A., Saez-Rodriguez J., McDermott U., Choudhary J.S.

Cell Rep. 20:2201-2214(2017).

Multi-omics of 34 colorectal cancer cell lines -- a resource for biomedical studies.

Myklebost O., Skotheim R.I., Sveen A., Lothe R.A.

Mol. Cancer 16:116.1-116.16(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).

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).

The molecular landscape of colorectal cancer cell lines unveils clinically actionable kinase targets.

Linnebacher M., Cordero F., Di Nicolantonio F., Bardelli A.

Nat. Commun. 6:7002.1-7002.10(2015).

Emergence of multiple EGFR extracellular mutations during cetuximab treatment in colorectal cancer.

Di Nicolantonio F., Albanell J., Bardelli A., Montagut C.

Clin. Cancer Res. 21:2157-2166(2015).

Epigenetic and genetic features of 24 colon cancer cell lines.";

Hektoen M., Lind G.E., Lothe R.A.

Oncogenesis 2:e71.1-e71.8(2013).

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).

5-fluorouracil response in a large panel of colorectal cancer cell lines is associated with mismatch repair deficiency.

Bracht K., Nicholls A.M., Liu Y., Bodmer W.F.

Br. J. Cancer 103:340-346(2010).

Genomic and biological characterization of exon 4 KRAS mutations in human cancer.

Lash A., Ladanyi M., Saltz L.B., Heguy A., Paty P.B., Solit D.B.

Cancer Res. 70:5901-5911(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).

Definitive molecular cytogenetic characterization of 15 colorectal cancer cell lines.

Camps J., McNeil N.E., Difilippantonio M.J., Ried T.

Genes Chromosomes Cancer 49:204-223(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).

Biology of colorectal and gastric cancer cell lines.";

Park J.-G., Gazdar A.F.

J. Cell. Biochem. Suppl. 24:131-141(1996).

NCI-Navy Medical Oncology Branch cell line data base.";

Carney D.N., Minna J.D., Mulshine J.L.

J. Cell. Biochem. Suppl. 24:32-91(1996).

Characteristics of cell lines established from human colorectal carcinoma.

Johnson B.E., Gazdar A.F.

Cancer Res. 47:6710-6718(1987).