GI-ME-NHomo sapiens (Human)Cancer cell line

Also known as: Gaslini Institute-ME-Neuroblastoma, Gimen1, Gimen, GIMEN, Gi-MEN, Gi-ME-N

🤖 AI SummaryBased on 15 publications

Quick Overview

Human neuroblastoma cell line with unique genetic features

Detailed Summary

GI-ME-N is a human neuroblastoma cell line established from the metastatic bone marrow of a 2-year-old patient with stage IV neuroblastoma. It exhibits distinct genetic characteristics, including a partial monosomy of the short arm of chromosome 1 (1p) and the absence of N-myc amplification. This cell line has been used in studies investigating the role of genetic alterations in neuroblastoma progression and drug resistance. Research on GI-ME-N has contributed to understanding the molecular mechanisms underlying neuroblastoma, particularly in relation to chromosomal abnormalities and their impact on tumor behavior. The cell line is also utilized in studies examining the effects of various treatments, including cytosine arabinoside, on cell differentiation and growth inhibition.

Research Applications

Genetic studies of neuroblastomaInvestigation of chromosomal abnormalitiesDrug resistance and treatment response studiesCell differentiation and growth inhibition research

Key Characteristics

Partial monosomy of 1pAbsence of N-myc amplificationHigh tumorigenicity in nude miceResponse to cytosine arabinoside treatment
Generated on 6/16/2025

Basic Information

Database IDCVCL_1232
SpeciesHomo sapiens (Human)
Tissue SourceBone marrow[UBERON:UBERON_0002371]

Donor Information

Age3
Age CategoryPediatric
SexFemale

Disease Information

DiseaseNeuroblastoma
LineagePeripheral Nervous System
SubtypeNeuroblastoma
OncoTree CodeNBL

DepMap Information

Source TypeDSMZ
Source IDACH-001344_source

Known Sequence Variations

TypeGene/ProteinDescriptionZygosityNoteSource
MutationUnexplicitNF1MicrodeletionHeterozygous-from parent cell line GI-ME-N
Gene deletionNF1-HeterozygousSomatic LOHPubMed=15207265

Haplotype Information (STR Profile)

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

Amelogenin
X
CSF1PO
11,12
D13S317
8,12
D16S539
9,12
D18S51
12,17
D19S433
13,14
D21S11
31
D2S1338
19,20
D3S1358
14
D5S818
12
D7S820
10,11
D8S1179
10,14
FGA
19,22
Penta D
9,13
Penta E
15,20
TH01
6,7
TPOX
11
vWA
16,19
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

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).

Prioritization of cancer therapeutic targets using CRISPR-Cas9 screens.

Stronach E.A., Saez-Rodriguez J., Yusa K., Garnett M.J.

Nature 568:511-516(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).

A landscape of pharmacogenomic interactions in cancer.";

Wessels L.F.A., Saez-Rodriguez J., McDermott U., Garnett M.J.

Cell 166:740-754(2016).

Testing of SNS-032 in a panel of human neuroblastoma cell lines with acquired resistance to a broad range of drugs.

Fichtner I., Ghafourian T., Westermann F., Cinatl J. Jr.

Transl. Oncol. 6:685-696(2013).

PEA15 impairs cell migration and correlates with clinical features predicting good prognosis in neuroblastoma.

Opoku-Ansah J., Wada R.K., Bachmann A.S., Ramos J.W.

Int. J. Cancer 131:1556-1568(2012).

NF1 is a tumor suppressor in neuroblastoma that determines retinoic acid response and disease outcome.

Messiaen L.M., Versteeg R., Bernards R.

Cell 142:218-229(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).

1H MRS identifies specific metabolite profiles associated with MYCN-amplified and non-amplified tumour subtypes of neuroblastoma cell lines.

Edwards E.C., Strachan M.C., McMullan D.J., Wilkes T.M., Grundy R.G.

NMR Biomed. 20:692-700(2007).

Combined M-FISH and CGH analysis allows comprehensive description of genetic alterations in neuroblastoma cell lines.

Salwen H.R., Laureys G., Manoel N., De Paepe A., Speleman F.

Genes Chromosomes Cancer 32:126-135(2001).

Analysis of 1;17 translocation breakpoints in neuroblastoma: implications for mapping of neuroblastoma genes.

van der Drift P., Chan A., Versteeg R., Speleman F.

Eur. J. Cancer 33:1974-1978(1997).

Comparative genomic hybridization analysis of human neuroblastomas: detection of distal 1p deletions and further molecular genetic characterization of neuroblastoma cell lines.

De Paepe A., Cremer T., Speleman F.

Cancer Genet. Cytogenet. 97:135-142(1997).

Deletion mapping in neuroblastoma cell lines suggests two distinct tumor suppressor genes in the 1p35-36 region, only one of which is associated with N-myc amplification.

Speleman F., Versteeg R.

Oncogene 10:291-297(1995).

New line of human neuroblastoma derived from bone marrow.";

Repetto G., Cornaglia-Ferraris P.

Pathologica 78:371-384(1986).

Cytogenetic and molecular study of two human neuroblastoma cell lines.

Cornaglia-Ferraris P.

Cancer Genet. Cytogenet. 30:225-231(1988).

Effect of cytosine arabinoside on the growth and phenotypic expression of GI-ME-N, a new human neuroblastoma cell line.

Cornaglia-Ferraris P.

Prog. Clin. Biol. Res. 271:437-448(1988).

N-myc amplification at chromosome band 1p32 in neuroblastoma cells as investigated by in situ hybridization.

Lampert F.

J. Cancer Res. Clin. Oncol. 114:636-640(1988).

Morphologic and phenotypic changes of human neuroblastoma cells in culture induced by cytosine arabinoside.

Cornaglia-Ferraris P.

Exp. Cell Res. 181:226-237(1989).

Chromosome 1 deletions in human neuroblastomas: generation and fine mapping of microclones from the distal 1p region.

Martinsson T., Weith A., Cziepluch C., Schwab M.

Genes Chromosomes Cancer 1:67-78(1989).

A new human highly tumorigenic neuroblastoma cell line with undetectable expression of N-myc.

Donti E., Di Martino D., Tonini G.P.

Pediatr. Res. 27:1-6(1990).

Tumor cell lines of the peripheral nervous system.";

Israel M.A., Thiele C.J.

(In book chapter) Atlas of human tumor cell lines; Hay R.J., Park J.-G., Gazdar A.F. (eds.); pp.43-78; Academic Press; New York; USA (1994).

Neuroblastoma.";

Thiele C.J.

(In book chapter) Human cell culture. Vol. 1. Cancer cell lines part 1; Masters J.R.W., Palsson B.O. (eds.); pp.21-53; Kluwer Academic Publishers; New York; USA (1999).