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Cellosaurus PM-1 [Human oral dysplasia] (CVCL_LN13)

[Text version]
Cell line name PM-1 [Human oral dysplasia]
Synonyms PM1
Accession CVCL_LN13
Resource Identification Initiative To cite this cell line use: PM-1 [Human oral dysplasia] (RRID:CVCL_LN13)
Comments Omics: Deep exome analysis.
Omics: Transcriptome analysis by microarray.
Derived from site: In situ; Forehead, skin; UBERON=UBERON_0016475.
Cell type: Keratinocyte; CL=CL_0000312.
Sequence variations
  • Mutation; HGNC; 5173; HRAS; Simple; p.Asn86Ser (c.257A>G); Zygosity=Unspecified (PubMed=24662767).
  • Mutation; HGNC; 7989; NRAS; Simple; p.Gly177Glu (c.530G>A); Zygosity=Unspecified (PubMed=24662767).
  • Mutation; HGNC; 11998; TP53; Simple; p.Glu258Lys (c.772G>A); ClinVar=VCV000012348; Zygosity=Unspecified (PubMed=24662767).
Disease Oral epithelial dysplasia (NCIt: C129863)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_LN09 ! MET-1
CVCL_LN10 ! MET-2
CVCL_LN11 ! MET-3
CVCL_LN12 ! MET-4
CVCL_VJ50 ! SCCT9
Sex of cell Male
Age at sampling 46Y
Category Transformed cell line
STR profile Source(s): PubMed=31336867

Markers:
AmelogeninX,Y
CSF1PO9,13
D2S133817,21
D3S135814
D5S81811,12
D7S8207,8
D8S117912,15
D13S3178,12
D16S53911,13
D18S5118,19
D19S43314
D21S1130.2,33.2
FGA24
TH018,9.3
TPOX9,11
vWA18,19

Run an STR similarity search on this cell line
Publications

PubMed=10772384; DOI=10.1034/j.1600-0625.2000.009002104.x
Proby C.M., Purdie K.J., Sexton C.J., Purkis P., Navsaria H.A., Stables J.N., Leigh I.M.
Spontaneous keratinocyte cell lines representing early and advanced stages of malignant transformation of the epidermis.
Exp. Dermatol. 9:104-117(2000)

PubMed=24662767; DOI=10.1038/jid.2014.154; PMCID=PMC4753672
South A.P., Purdie K.J., Watt S.A., Haldenby S., den Breems N.Y., Dimon M., Arron S.T., Kluk M.J., Aster J.C., McHugh A., Xue D.J., Dayal J.H.S., Robinson K.S., Rizvi S.M.H., Proby C.M., Harwood C.A., Leigh I.M.
NOTCH1 mutations occur early during cutaneous squamous cell carcinogenesis.
J. Invest. Dermatol. 134:2630-2638(2014)

PubMed=30202019; DOI=10.1038/s41467-018-06027-1; PMCID=PMC6131170
Inman G.J., Wang J., Nagano A., Alexandrov L.B., Purdie K.J., Taylor R.G., Sherwood V., Thomson J., Hogan S., Spender L.C., South A.P., Stratton M.R., Chelala C., Harwood C.A., Proby C.M., Leigh I.M.
The genomic landscape of cutaneous SCC reveals drivers and a novel azathioprine associated mutational signature.
Nat. Commun. 9:3667.1-3667.14(2018)

PubMed=31336867; DOI=10.3390/ijms20143428; PMCID=PMC6678499
Hassan S., Purdie K.J., Wang J., Harwood C.A., Proby C.M., Pourreyron C., Mladkova N., Nagano A., Dhayade S., Athineos D., Caley M., Mannella V., Blyth K., Inman G.J., Leigh I.M.
A Unique panel of patient-derived cutaneous squamous cell carcinoma cell lines provides a preclinical pathway for therapeutic testing.
Int. J. Mol. Sci. 20:3428.1-3428.26(2019)

Cross-references
Cell line collections (Providers) CancerTools; 153571
Ximbio; 153571
Encyclopedic resources Wikidata; Q54947601
Gene expression databases GEO; GSM2611476
GEO; GSM2611477
GEO; GSM2611478
Polymorphism and mutation databases Cosmic; 2688661
Entry history
Entry creation15-Nov-2017
Last entry update30-Jan-2024
Version number11