|
| Status |
Public on Jan 06, 2015 |
| Title |
EMT Alters Interstitial Fluid Flow-induced Signaling in ERBB2-positive Breast Cancer |
| Organism |
Homo sapiens |
| Experiment type |
Expression profiling by array
|
| Summary |
A variety of mechanotransduction forces are altered in the tumor microenvironment (TME) and these biophysical forces can influence cancer progression. One such force is interstitial fluid flow (IFF) - the movement of fluid through the tissue matrix. IFF was previously shown to induce invasion of cancer cells, but the activated signaling cascades remain poorly understood. Here, it is demonstrated that IFF induces invasion of ERBB2/HER2 expressing breast cancer cells via activation of phosphoinositide-3-kinase (PI3K). In constitutively activate ERBB2 expressing cells that have undergone epithelial-to-mesenchymal transition (EMT), IFF-mediated invasion requires the chemokine receptor CXCR4, a gradient of its ligand CXCL12, and activity of the PI3K catalytic subunits p110a and β. In wild-type ERBB2 expressing cells, IFF-mediated invasion is chemokine receptor-independent and requires only p110a activation. To test whether cells undergoing EMT alter their signaling response to IFF, TGFb1 was used to induce EMT in wild-type ERBB2-expressing cells resulting in IFF-induced invasion dependent on CXCR4 and p110β.
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| |
|
| Overall design |
2 cell lines (NeuN, NeuT), 2 conditions (flow, static), 3 replicates each, 12 samples total
|
| |
|
| Contributor(s) |
Tchafa AM |
| Citation(s) |
25566992 |
| Submission date |
Jan 05, 2015 |
| Last update date |
Aug 13, 2018 |
| Contact name |
Alimatou M Tchafa |
| E-mail(s) |
alima.tchafa@yahoo.fr
|
| Phone |
2672428234
|
| Organization name |
UT Southwestern Medical Center
|
| Department |
Biochemistry
|
| Lab |
Hamid Mirzaei
|
| Street address |
5323 Harry Hines Blvd, Rm Y4.306
|
| City |
Dallas |
| State/province |
TEXAS |
| ZIP/Postal code |
75390 |
| Country |
USA |
| |
|
| Platforms (1) |
| GPL10558 |
Illumina HumanHT-12 V4.0 expression beadchip |
|
| Samples (12)
|
|
| Relations |
| BioProject |
PRJNA271605 |
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