Lu-99Homo sapiens (Human)Cancer cell line

Also known as: C-Lu99, LU99, Lu99, Lu 99, LU-99

🤖 AI SummaryBased on 7 publications

Quick Overview

Lu-99 is a human lung cancer cell line with EGFR mutations and potential for drug sensitivity studies.

Detailed Summary

Lu-99 is a human lung cancer cell line derived from a giant cell carcinoma. It is known for harboring EGFR mutations, which are significant in the context of targeted therapies. The cell line has been used in studies examining the genetic heterogeneity of EGFR mutations and their implications for drug response. Research on Lu-99 has contributed to understanding the mechanisms of resistance and sensitivity to tyrosine kinase inhibitors like gefitinib. Additionally, it has been part of studies investigating the role of DCC gene expression and its association with cancer progression. The cell line's characteristics make it a valuable tool for studying lung cancer biology and therapeutic strategies.

Research Applications

EGFR mutation analysisDrug sensitivity studiesCancer biology researchGenetic heterogeneity studies

Key Characteristics

EGFR mutationsPotential for targeted therapy researchUsed in studies on drug resistancePart of DCC gene expression investigations
Generated on 6/19/2025

Basic Information

Database IDCVCL_3015
SpeciesHomo sapiens (Human)
Tissue SourceLung[UBERON:UBERON_0002048]

Donor Information

Age63
Age CategoryAdult
SexMale
Raceasian

Disease Information

DiseaseLung giant cell carcinoma
LineageLung
SubtypeGiant Cell Carcinoma of the Lung
OncoTree CodeGCLC

DepMap Information

Source TypeHSRRB
Source IDACH-000444_source

Known Sequence Variations

TypeGene/ProteinDescriptionZygosityNoteSource
MutationSimpleKRASp.Gly12Cys (c.34G>T)Unspecified-PubMed=21173094

Haplotype Information (STR Profile)

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

Amelogenin
X
CSF1PO
10,15
D13S317
10,11
D16S539
9
D5S818
12
D7S820
11
TH01
9
TPOX
11
vWA
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

Genetic diversity among the present Japanese population: evidence from genotyping of human cell lines established in Japan.

Kasai F., Fukushima M., Miyagi Y., Nakamura Y.

Hum. Cell 37:944-950(2024).

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).

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).

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).

Lack of AKT activation in lung cancer cells with EGFR mutation is a novel marker of cetuximab sensitivity.

Igishi T., Burioka N., Nanba E., Shimizu E.

Cancer Biol. Ther. 13:369-378(2012).

Genetic heterogeneity of the epidermal growth factor receptor in non-small cell lung cancer cell lines revealed by a rapid and sensitive detection system, the peptide nucleic acid-locked nucleic acid PCR clamp.

Fukuyama S., Yokote A., Kobayashi K., Kanazawa M., Hagiwara K.

Cancer Res. 65:7276-7282(2005).

Expression of tetraspanins in human lung cancer cells: frequent downregulation of CD9 and its contribution to cell motility in small cell lung cancer.

Hayashi S., Aozasa K., Kawase I.

Oncogene 22:674-687(2003).

Mutation and expression of the DCC gene in human lung cancer.";

Yokota J.

Neoplasia 2:300-305(2000).

Screening the p53 status of human cell lines using a yeast functional assay.

Mizusawa H., Tanaka N., Koyama H., Namba M., Kanamaru R., Kuroki T.

Mol. Carcinog. 19:243-253(1997).

Giant cell carcinomas of the lung producing colony-stimulating factor in vitro and in vivo.

Ogura T., Gamou S., Shimizu N.

Jpn. J. Cancer Res. 76:967-976(1985).