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Cellosaurus STA-ET-7.2 (CVCL_9693)

[Text version]
Cell line name STA-ET-7.2
Synonyms STA-ET-7_2; St. Anna Kinderspital-Ewing Tumor-7.2
Accession CVCL_9693
Resource Identification Initiative To cite this cell line use: STA-ET-7.2 (RRID:CVCL_9693)
Comments From: Children's Cancer Research Institute; Vienna; Austria.
Derived from site: Metastatic; Pleural effusion; UBERON=UBERON_0000175.
Sequence variations
Disease Ewing sarcoma (NCIt: C4817)
Ewing sarcoma (ORDO: Orphanet_319)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_9692 ! STA-ET-7.1
CVCL_9694 ! STA-ET-7.3
Category Cancer cell line
Publications

PubMed=8378080
Kovar H., Auinger A., Jug G., Aryee D.N.T., Zoubek A., Salzer-Kuntschik M., Gadner H.
Narrow spectrum of infrequent p53 mutations and absence of MDM2 amplification in Ewing tumours.
Oncogene 8:2683-2690(1993)

PubMed=9393981; DOI=10.1038/sj.onc.1201397
Kovar H., Jug G., Aryee D.N.T., Zoubek A., Ambros P.F., Gruber B., Windhager R., Gadner H.
Among genes involved in the RB dependent cell cycle regulatory cascade, the p16 tumor suppressor gene is frequently lost in the Ewing family of tumors.
Oncogene 15:2225-2232(1997)

PubMed=11507040
Kovar H., Jug G., Hattinger C.M., Spahn L., Aryee D.N.T., Ambros P.F., Zoubek A., Gadner H.
The EWS protein is dispensable for Ewing tumor growth.
Cancer Res. 61:5992-5997(2001)

Cross-references
Cell line databases/resources cancercelllines; CVCL_9693
Encyclopedic resources Wikidata; Q54955778
Polymorphism and mutation databases Cosmic; 1388899
IARC_TP53; 23648
Entry history
Entry creation06-Jun-2012
Last entry update19-Dec-2024
Version number13