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| Status |
Public on Sep 30, 2014 |
| Title |
Gene expression profiling of Notch1 knockout mouse liver samples and murine hepatic angiosarcoma cell lines. |
| Organism |
Mus musculus |
| Experiment type |
Expression profiling by array
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| Summary |
This work is part of the paper: Generation of a murine hepatic angiosarcoma cell line and reproducible mouse tumor model, Rothweiler S et al, Laboratory Investigation, 2014
Hepatic Angiosarcoma (AS) is a rare and highly aggressive tumor of endothelial origin with dismal prognosis. Studies of the molecular biology of AS and treatment options are limited since animal models are rare. We have previously shown that inducible knockout of Notch1 in mice leads to spontaneous formation of hepatic AS. The aim of this study was to 1) establish and characterize a cell line derived from this murine AS, 2) to identify molecular pathways involved in the pathogenesis and potential therapeutic targets, and 3) to generate a tumor transplantation model. AS cells retained specific endothelial properties such as tube formation activity, as well as expression of CD31 and von Willebrand Factor. However, electron microscopy analysis revealed signs of dedifferentiation with loss of fenestrae and loss of contact inhibition. Microarray and pathway analysis showed substantial changes in gene expression and revealed activation of the Myc pathway. Exposing the AS cells to sorafenib reduced migration, filopodia dynamics, and cell proliferation but did not induce apoptosis. In addition, sorafenib suppressed ERK phosphorylation and expression of cyclin D2. Injection of AS cells into NOD/SCID mice resulted in formation of undifferentiated tumors confirming the tumorigenic potential of these cells. Conclusion: We established and characterized a murine model of spontaneous AS formation and hepatic AS cell lines as a useful in vitro tool. Our data demonstrate antitumor activity of sorafenib in AS cells with potent inhibition of migration, filopodia formation, and cell proliferation, which support further evaluation of sorafenib as a novel treatment strategy. In addition, AS cell transplantation provides a subcutaneous tumor model useful for in vivo preclinical drug testing.
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| Overall design |
Mouse liver samples (Notch1 knockout and wild type control, 3 animals per group) and angiosarcoma cell lines (3 independently derived lines) were analyzed.
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| Contributor(s) |
Rothweiler S, Dill MT, Terraciano L, Makowska Z, Quagliata L, Hlushchuk R, Djonov V, Heim MH, Semela D |
| Citation(s) |
25418579 |
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| Submission date |
May 14, 2014 |
| Last update date |
Mar 04, 2019 |
| Contact name |
Zuzanna Makowska |
| Organization name |
University of Basel
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| Department |
Biomedicine
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| Lab |
Hepatology
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| Street address |
Hebelstrasse 20
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| City |
Basel |
| ZIP/Postal code |
4031 |
| Country |
Switzerland |
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| Platforms (1) |
| GPL6246 |
[MoGene-1_0-st] Affymetrix Mouse Gene 1.0 ST Array [transcript (gene) version] |
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| Samples (9)
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| GSM1386005 |
mouse liver sample, WT strain, biological replicate 1 |
| GSM1386006 |
mouse liver sample, WT strain, biological replicate 2 |
| GSM1386007 |
mouse liver sample, WT strain, biological replicate 3 |
| GSM1386008 |
mouse liver sample, KO strain, biological replicate 1 |
| GSM1386009 |
mouse liver sample, KO strain, biological replicate 2 |
| GSM1386010 |
mouse liver sample, KO strain, biological replicate 3 |
| GSM1386011 |
mouse hepatic angiosarcoma cell line, biological replicate 1 |
| GSM1386012 |
mouse hepatic angiosarcoma cell line, biological replicate 2 |
| GSM1386013 |
mouse hepatic angiosarcoma cell line, biological replicate 3 |
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| Relations |
| BioProject |
PRJNA247459 |
| Supplementary file |
Size |
Download |
File type/resource |
| GSE57655_RAW.tar |
38.4 Mb |
(http)(custom) |
TAR (of CEL) |
| Processed data included within Sample table |
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