STM91-01Homo sapiens (Human)Cancer cell line

Also known as: STM9101, STM-91-01

AI Summary

No AI-generated summary available for this cell line.

Basic Information

Database IDCVCL_8000
SpeciesHomo sapiens (Human)
Tissue SourceLung[UBERON:UBERON_0002048]

Donor Information

0
Age CategoryPediatric
SexMale

Disease Information

DiseaseRhabdoid tumor
LineageKidney
SubtypeRhabdoid Cancer
OncoTree CodeMRT

DepMap Information

Source TypeAcademic lab
Source IDACH-001200_source

Known Sequence Variations

TypeGene/ProteinDescriptionZygosityNoteSource
Gene deletionSMARCB1-Homozygous-PubMed=11921280

Haplotype Information (STR Profile)

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

Amelogenin
X,Y
CSF1PO
10,12
D13S317
9,12
D16S539
11,13
D18S51
12,17
D21S11
29,31
D3S1358
15,16
D5S818
10,11
D7S820
11
D8S1179
10,15
FGA
22,26
Penta D
10,17
Penta E
5,16
TH01
7
TPOX
8,11
vWA
16,17
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

Next-generation characterization of the Cancer Cell Line Encyclopedia.

Sellers W.R.

Nature 569:503-508(2019).

Genome-wide approach to identify second gene targets for malignant rhabdoid tumors using high-density oligonucleotide microarrays.

Ogawa S.

Cancer Sci. 105:258-264(2014).

Prognostic significance of dysadherin expression in epithelioid sarcoma and its diagnostic utility in distinguishing epithelioid sarcoma from malignant rhabdoid tumor.

Saito T., Yamamoto H., Tamiya S., Iwamoto Y., Tsuneyoshi M.

Mod. Pathol. 19:820-831(2006).

Expression of pericyte, mesangium and muscle markers in malignant rhabdoid tumor cell lines: differentiation-induction using 5-azacytidine.

Sugita K.

Cancer Sci. 94:1059-1065(2003).

Malignant rhabdoid tumor shows incomplete neural characteristics as revealed by expression of SNARE complex.

Yoshida S., Narita T., Taga T., Ohta S., Takeuchi Y.

J. Neurosci. Res. 69:642-652(2002).

Aberrations of the hSNF5/INI1 gene are restricted to malignant rhabdoid tumors or atypical teratoid/rhabdoid tumors in pediatric solid tumors.

Gilles F.H., Sugita K., Abe S., Sako M., Hashizume K., Hayashi Y.

Genes Chromosomes Cancer 34:33-41(2002).

Subcellular distribution of cytokeratin and vimentin in malignant rhabdoid tumor: three-dimensional imaging with confocal laser scanning microscopy and double immunofluorescence.

Oshiro Y., Oda Y., Ohta S., Furue M., Tsuneyoshi M.

Mod. Pathol. 14:854-861(2001).

Cloning and characterization of a novel Rab-family gene, Rab36, within the region at 22q11.2 that is homozygously deleted in malignant rhabdoid tumors.

Nakamura Y., Inazawa J.

Biochem. Biophys. Res. Commun. 254:594-600(1999).

Gene expression of malignant rhabdoid tumor cell lines by reverse transcriptase-polymerase chain reaction.

Suzuki A., Ohta S., Shimada M.

Diagn. Mol. Pathol. 6:326-332(1997).

Narrowing the critical region for a rhabdoid tumor locus in 22q11.";

Bell C.J.

Genes Chromosomes Cancer 16:94-105(1996).

Malignant rhabdoid tumor. A study with two established cell lines.";

Ota S., Crabbe D.C.G., Tran T.N., Triche T.J., Shimada H.

Cancer 71:2862-2872(1993).