NCC-ITHomo sapiens (Human)Cancer cell line

Also known as: NCCIT, NCC15

🤖 AI SummaryBased on 4 publications

Quick Overview

Human germ cell tumor cell line with cisplatin resistance mutations.

Detailed Summary

The NCC-IT cell line is a human germ cell tumor cell line derived from testicular tissue. It is known for its resistance to cisplatin, a common chemotherapy drug. Research has identified mutations in several genes, including FGFR3, AKT1, PIK3CA, and KRAS, which may contribute to this resistance. These mutations are associated with the PI3K-AKT signaling pathway, suggesting potential targets for therapeutic intervention. The cell line is used in studies investigating the molecular mechanisms of cisplatin resistance and the development of targeted therapies for testicular germ cell tumors.

Research Applications

Cisplatin resistance mechanismsMutational analysis in cancerTargeted therapy development

Key Characteristics

Cisplatin-resistantMutations in PI3K-AKT pathway genesUsed in studying germ cell tumor biology
Generated on 6/17/2025

Basic Information

Database IDCVCL_1451
SpeciesHomo sapiens (Human)

Donor Information

Age24
Age CategoryAdult
SexMale

Disease Information

DiseaseNon-central nervous system-localized embryonal carcinoma
LineageTestis
SubtypeEmbryonal Carcinoma
OncoTree CodeEMBCA

DepMap Information

Source TypeATCC
Source IDACH-001578_source

Known Sequence Variations

TypeGene/ProteinDescriptionZygosityNoteSource
MutationSimpleTP53p.Val272Cysfs*73 (c.814delG)Homozygous-from parent cell line NCC-IT
MutationSimplePTENp.Arg173Pro (c.518G>C)Heterozygous-from parent cell line NCC-IT
MutationSimpleMAP2K4p.Lys309Asn (c.927G>C)Unspecified-from parent cell line NCC-IT

Haplotype Information (STR Profile)

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

Amelogenin
X
CSF1PO
10,12
D13S317
11
D16S539
9,12
D18S51
13,14
D21S11
29,32.2
D3S1358
16
D5S818
10,13
D7S820
10
D8S1179
10,15
FGA
22,26
Penta D
10,12
Penta E
5,14
TH01
7,9
TPOX
8
vWA
14,18
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).

Proteomic profiling of cisplatin-resistant and cisplatin-sensitive germ cell tumour cell lines using quantitative mass spectrometry.

Strobel P., Kueffer S., Nettersheim D., Bremmer F.

World J. Urol. 40:373-383(2022).

Molecular basis of cisplatin resistance in testicular germ cell tumors.

Buchler T., Trka J., Boublikova L.

Cancers (Basel) 11:1316.1-1316.18(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).

Presence of somatic mutations within PIK3CA, AKT, RAS, and FGFR3 but not BRAF in cisplatin-resistant germ cell tumors.

Reuter V.E., Bosl G.J., Chaganti R.S.K., Solit D.B.

Clin. Cancer Res. 20:3712-3720(2014).

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).

Human mitogen-activated protein kinase kinase 4 as a candidate tumor suppressor.

Skolnick M.H., Tavtigian S.V.

Cancer Res. 57:4177-4182(1997).

Four new human germ cell tumor cell lines.";

Kanazawa H., Kakizoe T.

Lab. Invest. 59:328-336(1988).

Web Resources