Rh41Homo sapiens (Human)Cancer cell line

Also known as: SJ-Rh41, Rh-41, RH-41, RH41

🤖 AI SummaryBased on 11 publications

Quick Overview

Rh41 is a human rhabdomyosarcoma cell line used in cancer research.

Detailed Summary

Rh41 is a human rhabdomyosarcoma cell line derived from a lung metastasis in a 7-year-old female. It is classified as an alveolar rhabdomyosarcoma (ARMS) and is characterized by the presence of PAX-FKHR fusion transcripts. This cell line is commonly used in studies related to sarcoma biology, drug screening, and molecular profiling. Rh41 has been utilized in research to investigate the effects of various anticancer agents and to understand the genetic and molecular mechanisms underlying rhabdomyosarcoma progression. It is part of a panel of cell lines used for in vitro cytotoxicity testing and has been involved in studies examining gene expression profiles and therapeutic responses.

Research Applications

Sarcoma biologyDrug screeningMolecular profilingIn vitro cytotoxicity testing

Key Characteristics

PAX-FKHR fusion transcriptsAlveolar rhabdomyosarcoma subtypeLung metastasis origin
Generated on 6/18/2025

Basic Information

Database IDCVCL_2176
SpeciesHomo sapiens (Human)
Tissue SourceLung[UBERON:UBERON_0002048]

Donor Information

Age7
Age CategoryPediatric
SexFemale

Disease Information

DiseaseAlveolar rhabdomyosarcoma
LineageSoft Tissue
SubtypeAlveolar Rhabdomyosarcoma
OncoTree CodeARMS

DepMap Information

Source TypeDSMZ
Source IDACH-000100_source

Known Sequence Variations

TypeGene/ProteinDescriptionZygosityNoteSource
Gene fusionFOXO1PAX3-FOXO1, PAX3-FKHR-Not found in original tumorfrom parent cell line Rh30

Haplotype Information (STR Profile)

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

Amelogenin
X
CSF1PO
11,12
D13S317
8,9
D16S539
12,13
D18S51
15,16
D19S433
13,15
D21S11
29,31
D2S1338
17,21
D3S1358
17
D5S818
10,13
D7S820
10,11
D8S1179
10,13
FGA
20,22
Penta D
9,12
Penta E
11,17
TH01
7,9.3
TPOX
8,11
vWA
16,18
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

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).

Assessing alveolar rhabdomyosarcoma cell lines as tumor models by comparison of mRNA expression profiles.

Batchu S., Kellish A.S., Hakim A.A.

Gene 760:145025.1-145025.5(2020).

Quantitative proteomics of the Cancer Cell Line Encyclopedia.";

Sellers W.R., Gygi S.P.

Cell 180:387-402.e16(2020).

Proteomic profiling of rhabdomyosarcoma-derived exosomes yield insights into their functional role in paracrine signaling.

Diab-Assaf M., Saab R., Ghayad S.E.

J. Proteome Res. 18:3567-3579(2019).

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).

A landscape of pharmacogenomic interactions in cancer.";

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

Cell 166:740-754(2016).

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).

Sarcoma cell line screen of oncology drugs and investigational agents identifies patterns associated with gene and microRNA expression.

Harris E., Monks A., Morris J.

Mol. Cancer Ther. 14:2452-2462(2015).

Human rhabdomyosarcoma cell lines for rhabdomyosarcoma research: utility and pitfalls.

Linardic C.M.

Front. Oncol. 3:183.1-183.12(2013).

Proof-of-concept rare cancers in drug development: the case for rhabdomyosarcoma.

Sokolowski E., Turina C.B., Kikuchi K., Langenau D.M., Keller C.

Oncogene 33:1877-1889(2014).

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).

Oncogene mutation profiling of pediatric solid tumors reveals significant subsets of embryonal rhabdomyosarcoma and neuroblastoma with mutated genes in growth signaling pathways.

Borsu L., Barr F.G., Ladanyi M.

Clin. Cancer Res. 18:748-757(2012).

National Cancer Institute pediatric preclinical testing program: model description for in vitro cytotoxicity testing.

Reynolds C.P.

Pediatr. Blood Cancer 56:239-249(2011).

Genomic imbalances in rhabdomyosarcoma cell lines affect expression of genes frequently altered in primary tumors: an approach to identify candidate genes involved in tumor development.

Pritchard-Jones K., Kool M., Shipley J.M.

Genes Chromosomes Cancer 48:455-467(2009).

Global gene expression profiling of PAX-FKHR fusion-positive alveolar and PAX-FKHR fusion-negative embryonal rhabdomyosarcomas.

Olshen A.B., Barr F.G., Ladanyi M.

J. Pathol. 212:143-151(2007).

Pediatric rhabdomyosarcoma cell lines are resistant to Fas-induced apoptosis and highly sensitive to TRAIL-induced apoptosis.

Petak I., Douglas L., Tillman D.M., Vernes R., Houghton J.A.

Clin. Cancer Res. 6:4119-4127(2000).