Veterinärmedizinische Universität Wien Forschungsinformationssystem VetDoc

Grafischer Link zur Startseite der Vetmeduni Vienna

Gewählte Publikation:

Open Access Logo

Publikationstyp: Zeitschriftenaufsatz
Dokumenttyp: Originalarbeit

Jahr: 2017

AutorInnen: Minas, TZ; Surdez, D; Javaheri, T; Tanaka, M; Howarth, M; Kang, HJ; Han, J; Han, ZY; Sax, B; Kream, BE; Hong, SH; Çelik, H; Tirode, F; Tuckermann, J; Toretsky, JA; Kenner, L; Kovar, H; Lee, S; Sweet-Cordero, EA; Nakamura, T; Moriggl, R; Delattre, O; Üren, A

Titel: Combined experience of six independent laboratories attempting to create an Ewing sarcoma mouse model.

Quelle: Oncotarget. 2017; 8(21):34141-34163



Autor/innen der Vetmeduni Vienna:

Kenner Lukas
Moriggl Richard

Beteiligte Vetmed-Organisationseinheiten
Institut für Tierzucht und Genetik, Abteilung für Funktionelle Krebsgenomik
Institut für Pathologie, Abteilung für Labortierpathologie


Abstract:
Ewing sarcoma (ES) involves a tumor-specific chromosomal translocation that produces the EWS-FLI1 protein, which is required for the growth of ES cells both in vitro and in vivo. However, an EWS-FLI1-driven transgenic mouse model is not currently available. Here, we present data from six independent laboratories seeking an alternative approach to express EWS-FLI1 in different murine tissues. We used the Runx2, Col1a2.3, Col1a3.6, Prx1, CAG, Nse, NEFL, Dermo1, P0, Sox9 and Osterix promoters to target EWS-FLI1 or Cre expression. Additional approaches included the induction of an endogenous chromosomal translocation, in utero knock-in, and the injection of Cre-expressing adenovirus to induce EWS-FLI1 expression locally in multiple lineages. Most models resulted in embryonic lethality or developmental defects. EWS-FLI1-induced apoptosis, promoter leakiness, the lack of potential cofactors, and the difficulty of expressing EWS-FLI1 in specific sites were considered the primary reasons for the failed attempts to create a transgenic mouse model of ES.

Keywords Pubmed: Adenoviridaegenetics
Animals
Cell Line, Tumor
Disease Models, Animal
Gene Expression Regulation, Neoplastic
Gene Knock-In Techniques
Humans
Mice
Mice, Transgenic
Neoplasm Transplantation
Oncogene Proteins, Fusiongenetics
Promoter Regions, Genetic
Proto-Oncogene Protein c-fli-1genetics
RNA-Binding Protein EWSgenetics
Sarcoma, Ewinggeneticspathology

© Veterinärmedizinische Universität Wien Hilfe und DownloadsErklärung zur Barrierefreiheit