Mero-84Homo sapiens (Human)Cancer cell line

Also known as: MERO84

🤖 AI SummaryBased on 2 publications

Quick Overview

Human malignant mesothelioma cell line for cancer research.

Detailed Summary

Mero-84 is a human malignant mesothelioma cell line established from tumor samples. It exhibits abnormal karyotypes and expresses epithelial membrane antigen (EMA). The cell line shows variable doubling times and does not undergo senescence. Cytogenetic analysis indicates chromosomal abnormalities, and it is used in studies of mesothelioma biology and therapeutic development. Mero-84 is also implicated in Hippo pathway research due to mutations in genes like NF2 and LATS2, highlighting its relevance in understanding tumor progression and potential targeted therapies.

Research Applications

Cancer researchMesothelioma biologyTherapeutic developmentHippo pathway studies

Key Characteristics

Abnormal karyotypesEMA expressionVariable doubling timesNo senescenceChromosomal abnormalities
Generated on 6/19/2025

Basic Information

Database IDCVCL_2596
SpeciesHomo sapiens (Human)
Tissue SourcePleural effusion[UBERON:UBERON_0000175]

Donor Information

Age CategoryUnknown
SexMale

Disease Information

DiseasePleural mesothelioma
LineagePleura
SubtypePleural Mesothelioma, Biphasic Type
OncoTree CodePLBMESO

DepMap Information

Source TypeSigma-Aldrich
Source IDACH-001561_source

Haplotype Information (STR Profile)

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

Amelogenin
X
CSF1PO
10,11
D13S317
8,12
D16S539
9
D18S51
15,16
D21S11
29,31,32
D3S1358
16
D5S818
11
D7S820
9,11
D8S1179
12
FGA
19
Penta D
10,13
Penta E
7,11
TH01
9
TPOX
9,11
vWA
14,17
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

Hippo pathway gene mutations in malignant mesothelioma: revealed by RNA and targeted exon sequencing.

Asamura H., Gemma A., Yamada T.

J. Thorac. Oncol. 10:844-851(2015).

Establishment of human malignant mesothelioma cell lines.";

Delahaye M., Hagemeijer A.

Int. J. Cancer 44:256-260(1989).