LN-443Homo sapiens (Human)Cancer cell line

Also known as: LN443, LN 443

🤖 AI SummaryBased on 6 publications

Quick Overview

Human glioblastoma cell line with p53, p16, and PTEN mutations.

Detailed Summary

LN-443 is a human glioblastoma cell line derived from a male patient with a median age of 66 years. It exhibits mutations in the TP53, p16, and PTEN genes, which are frequently altered in glioblastomas. These genetic alterations suggest a role in the development and progression of glioblastomas. The cell line is used in research to study the molecular mechanisms of glioma biology and to evaluate therapeutic strategies targeting these genetic alterations. LN-443 has been characterized for its tumorigenic potential and is part of a panel of glioma cell lines used to investigate the genetic diversity and functional consequences of these mutations.

Research Applications

Genetic analysis of glioblastoma mutationsTumorigenicity studiesTherapeutic target evaluation

Key Characteristics

TP53 mutationp16 deletionPTEN mutation
Generated on 6/20/2025

Basic Information

Database IDCVCL_3960
SpeciesHomo sapiens (Human)
Tissue SourceBrain, left parietal lobe[UBERON:UBERON_0002802]

Donor Information

Age CategoryUnknown
SexFemale

Disease Information

DiseaseGlioblastoma
LineageCNS/Brain
SubtypeGlioblastoma
OncoTree CodeGB

DepMap Information

Source TypeAcademic lab
Source IDACH-000673_source

Known Sequence Variations

TypeGene/ProteinDescriptionZygosityNoteSource
MutationSimpleTP53p.His214Arg (c.641A>G)Unspecified-Unknown

Haplotype Information (STR Profile)

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

Amelogenin
X
CSF1PO
10,12
D13S317
8
D16S539
10,11
D18S51
15,16
D21S11
28,30
D3S1358
15,17
D5S818
9,12
D7S820
10
D8S1179
13,14
FGA
21,23
Penta D
11,12
Penta E
7,13
TH01
7,9
TPOX
8
vWA
18,19
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

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).

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).

DNA fingerprinting of glioma cell lines and considerations on similarity measurements.

Hamou M.-F., Delorenzi M., Hegi M.E.

Neuro-oncol. 14:701-711(2012).

Effect of aberrant p53 function on temozolomide sensitivity of glioma cell lines and brain tumor initiating cells from glioblastoma.

Cairncross J.G.

J. Neurooncol. 102:1-7(2011).

Frequent co-alterations of TP53, p16/CDKN2A, p14ARF, PTEN tumor suppressor genes in human glioma cell lines.

Van Meir E.G.

Brain Pathol. 9:469-479(1999).

The human melanoma antigen-encoding gene, MAGE-1, is expressed by other tumour cells of neuroectodermal origin such as glioblastomas and neuroblastomas.

Rimoldi D., Romero P., Carrel S.

Int. J. Cancer 54:527-528(1993).

Variant CD44 adhesion molecules are expressed in human brain metastases but not in glioblastomas.

Diserens A.-C., Van Meir E.G.

Cancer Res. 53:5345-5349(1993).

Web Resources