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Status |
Public on Jun 15, 2016 |
Title |
Expression data from ELK3 knocked down MDA-MB-231 cell line. |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by array
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Summary |
Triple-negative breast cancer is a highly aggressive tumor subtype that lacks effective therapeutic targets. Here, we show that ELK3 is overexpressed in a subset of breast cancers, in particular basal-like and normal-like/claudin-low cell lines. Suppression of ELK3 in MDA-MB-231 cells led to transdifferentiation from an invasive mesenchymal phenotype to a non-invasive epithelial phenotype both in vitro and in vivo. Suppression of ELK3 results in the extensive changes in genome expression profiles. Among these, GATA3, a master suppressor of metastasis, was epigenetically activated and we found that suppression of GATA3 led to the restoration of migration and invasion. These results suggest that the ELK3-GATA3 axis is a major pathway that promotes metastasis of MDA-MB-231 cells.
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Overall design |
Retrovirus expressing shRNA of ELK3 was transduced into MDA-MB-231 cell line and stable cell line of which ELK3 is suppressed more than 50% was selected by the drug selection (Puromycin).
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Contributor(s) |
Park K, Kim K |
Citation missing |
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Submission date |
Jun 14, 2016 |
Last update date |
Aug 23, 2018 |
Contact name |
Jae Yong Lee |
Organization name |
Cha Unniversity
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Street address |
335, Pangyo-ro
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City |
SungNam |
ZIP/Postal code |
13488 |
Country |
South Korea |
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Platforms (1) |
GPL15207 |
[PrimeView] Affymetrix Human Gene Expression Array |
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Samples (4)
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GSM2199543 |
Stable MDA-MB-231 cell line established by the integration of control shRNA, Biological repeat 1 |
GSM2199546 |
Stable MDA-MB-231 cell line established by the integration of control shRNA, Biological repeat 2 |
GSM2199547 |
Stable MDA-MB-231 cell line established by the integration of shRNA targeting to ELK3, Biological repeat 1 |
GSM2199548 |
Stable MDA-MB-231 cell line established by the integration of shRNA targeting to ELK3, Biological repeat 2 |
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Relations |
BioProject |
PRJNA325597 |