NCI-H2452Homo sapiens (Human)Cancer cell line

Also known as: NCIH2452, H-2452, H2452

🤖 AI SummaryBased on 14 publications

Quick Overview

Malignant mesothelioma cell line with BAP1 mutations and Hippo pathway alterations.

Detailed Summary

The NCI-H2452 cell line is a malignant mesothelioma cell line derived from human tissue. It is characterized by mutations in the BAP1 gene, which is involved in the Hippo signaling pathway. These mutations contribute to the inactivation of tumor suppressor functions, leading to uncontrolled cell proliferation. Research on this cell line has focused on understanding the role of BAP1 and other Hippo pathway components in mesothelioma progression and therapeutic resistance. The cell line is used to study the molecular mechanisms underlying mesothelioma and to develop targeted therapies.

Research Applications

Cancer biologyGenomic analysisTherapeutic target identificationHippo pathway studies

Key Characteristics

BAP1 mutationsHippo pathway alterationsMalignant mesothelioma model
Generated on 6/17/2025

Basic Information

Database IDCVCL_1553
SpeciesHomo sapiens (Human)
Tissue SourceLung, pleura[UBERON:UBERON_0000977]

Donor Information

Age CategoryAdult
SexMale

Disease Information

DiseasePleural mesothelioma
LineagePleura
SubtypePleural Mesothelioma, Biphasic Type
OncoTree CodePLBMESO

DepMap Information

Source TypeATCC
Source IDACH-000092_source

Known Sequence Variations

TypeGene/ProteinDescriptionZygosityNoteSource
MutationSimpleBAP1p.Ala95Asp (c.284C>A)Heterozygous-PubMed=26011428, PubMed=21642991
Gene deletionCDKN2A-HomozygousPossiblePubMed=26870271
Gene deletionBAP1-Heterozygous-PubMed=21642991

Haplotype Information (STR Profile)

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

Amelogenin
X,Y
CSF1PO
11,12
D12S391
17.3,21
D13S317
12
D16S539
11,13
D18S51
15
D19S433
13
D21S11
28,32.2
D2S1338
20
D3S1358
17
D5S818
11,12
D6S1043
11,12
D7S820
9,11
D8S1179
10
FGA
23
Penta D
9
Penta E
12,15
TH01
6,9.3
TPOX
8,11
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).

From clinical specimens to human cancer preclinical models -- a journey the NCI-cell line database-25 years later.

Aldige C.R., Wistuba I.I., Minna J.D.

J. Cell. Biochem. 121:3986-3999(2020).

Comprehensive transcriptomic analysis of cell lines as models of primary tumors across 22 tumor types.

van 't Veer L.J., Butte A.J., Goldstein T., Sirota M.

Nat. Commun. 10:3574.1-3574.11(2019).

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).

Chemistry-first approach for nomination of personalized treatment in lung cancer.

Posner B.A., Minna J.D., Kim H.S., White M.A.

Cell 173:864-878.e29(2018).

E-cadherin expression is correlated with focal adhesion kinase inhibitor resistance in merlin-negative malignant mesothelioma cells.

Kato T., Sato T., Yokoi K., Sekido Y.

Oncogene 36:5522-5531(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).

Functional differences between wild-type and mutant-type BRCA1-associated protein 1 tumor suppressor against malignant mesothelioma cells.

Yokoi K., Sekido Y.

Cancer Sci. 106:990-999(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).

Hippo pathway gene mutations in malignant mesothelioma: revealed by RNA and targeted exon sequencing.

Asamura H., Gemma A., Yamada T.

J. Thorac. Oncol. 10:844-851(2015).

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

Neve R.M.

Nature 520:307-311(2015).

A comprehensive transcriptional portrait of human cancer cell lines.

Settleman J., Seshagiri S., Zhang Z.-M.

Nat. Biotechnol. 33:306-312(2015).

Frequent coamplification and cooperation between C-MYC and PVT1 oncogenes promote malignant pleural mesothelioma.

Rice D.C., Tsao A., Wistuba I.I.

J. Thorac. Oncol. 9:998-1007(2014).

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).

The nuclear deubiquitinase BAP1 is commonly inactivated by somatic mutations and 3p21.1 losses in malignant pleural mesothelioma.

Powell S.N., Zhou Q., Shen R.-L., Olshen A.B., Rusch V.W., Ladanyi M.

Nat. Genet. 43:668-672(2011).

LATS2 is a tumor suppressor gene of malignant mesothelioma.";

Sekido Y.

Cancer Res. 71:873-883(2011).

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).

Protein expression of the RB-related gene family and SV40 large T antigen in mesothelioma and lung cancer.

Modi S., Kubo A., Oie H.K., Coxon A.B., Rehmatulla A., Kaye F.J.

Oncogene 19:4632-4639(2000).

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 nine newly derived mesothelioma cell lines.";

Mew D.J.Y., Pogrebniak H.W., Matthews W.J.

Ann. Thorac. Surg. 59:835-844(1995).