S462Homo sapiens (Human)Cancer cell line

Also known as: Patient 6 cell line

🤖 AI SummaryBased on 6 publications

Quick Overview

Human cell line derived from malignant peripheral nerve sheath tumor, used in cancer research.

Detailed Summary

The S462 cell line is a human-derived cell line established from a malignant peripheral nerve sheath tumor (MPNST). It is utilized in research to study the molecular mechanisms and therapeutic strategies for MPNST, a rare and aggressive soft tissue sarcoma. The cell line has been characterized in multiple studies for its genetic and molecular profiles, including alterations in tumor suppressor genes and oncogenes. Research involving S462 has explored its response to various therapeutic agents, including HDAC inhibitors and targeted therapies, highlighting its utility in preclinical drug testing and understanding tumor biology. The cell line is also used to investigate the role of specific genes and pathways in tumor progression and resistance to treatment.

Research Applications

Cancer researchDrug screeningMolecular mechanisms of tumor progressionTherapeutic target identification

Key Characteristics

Expresses EGFR and erbB2Genetic alterations in tumor suppressor genes (e.g., NF1, TP53)Response to HDAC inhibitors and targeted therapiesUsed in preclinical studies for MPNST
Generated on 6/18/2025

Basic Information

Database IDCVCL_1Y70
SpeciesHomo sapiens (Human)
Tissue SourceThigh[UBERON:UBERON_0000376]

Donor Information

Age CategoryUnknown
SexFemale
Subtype FeaturesNF1_Mutant

Disease Information

DiseaseNeurofibromatosis type 1
LineagePeripheral Nervous System
SubtypeMalignant Peripheral Nerve Sheath Tumor
OncoTree CodeMPNST

DepMap Information

Source TypeAcademic lab
Source IDACH-002693_source

Known Sequence Variations

TypeGene/ProteinDescriptionZygosityNoteSource
MutationSimpleTP53p.Arg110Pro (c.329G>C)Heterozygous-from parent cell line S462
MutationSimpleNF1p.Tyr2285Ter (c.6792C>A)Heterozygous-from parent cell line S462
Gene deletionTP53-Homozygous2 out of 3 copiesfrom parent cell line HL-60
Gene deletionNF1-HeterozygousSomatic LOHPubMed=15207265

Haplotype Information (STR Profile)

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

Amelogenin
X
CSF1PO
12,13
D13S317
12
D16S539
13
D18S51
16
D19S433
14
D21S11
29,31
D2S1338
23
D3S1358
14,17
D5S818
12,13
D7S820
8,10
D8S1179
10,12
FGA
20
Penta D
9,11
Penta E
11
TH01
8
TPOX
8
vWA
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

Genetics of human malignant peripheral nerve sheath tumors.";

Pemov A., Li H., Presley W., Wallace M.R., Miller D.T.

Neurooncol. Adv. 2:i50-i61(2020).

Drug sensitivity and resistance testing identifies PLK1 inhibitors and gemcitabine as potent drugs for malignant peripheral nerve sheath tumors.

Lothe R.A.

Mol. Oncol. 11:1156-1171(2017).

Sensitivity of malignant peripheral nerve sheath tumor cells to TRAIL is augmented by loss of NF1 through modulation of MYC/MAD and is potentiated by curcumin through induction of ROS.

Mautner V.-F., von Deimling A.

PLoS ONE 8:E57152-E57152(2013).

Cancer stem cell-like cells derived from malignant peripheral nerve sheath tumors.

Mautner V.-F., Rabkin S.D., Demestre M.

PLoS ONE 6:E21099-E21099(2011).

Autophagic survival in resistance to histone deacetylase inhibitors: novel strategies to treat malignant peripheral nerve sheath tumors.

Lev D.C.

Cancer Res. 71:185-196(2011).

EGFR and erbB2 in malignant peripheral nerve sheath tumors and implications for targeted therapy.

Mautner V.-F., Schildhaus H.-U., von Deimling A.

Neuro-oncol. 10:946-957(2008).

Differential modulation of malignant peripheral nerve sheath tumor growth by omega-3 and omega-6 fatty acids.

Mautner V.-F., Kindler-Rohrborn A., Kurtz A.

Oncogene 24:2367-2374(2005).

Genetic and phenotypic characterization of tumor cells derived from malignant peripheral nerve sheath tumors of neurofibromatosis type 1 patients.

Friedrich R.E., Knoefel W.T., Peiper M., Kluwe L.

Neurobiol. Dis. 16:85-91(2004).