Abstract
Background: The interaction of SDF-1alpha with its receptor CXCR4 plays a role in the occurrence of distant metastasis in many solid tumors. This interaction increases migration from primary sites as well as homing at distant sites. Methods: Here we investigated how SDF-1aα could modulate both migration and adhesion of cancer cells through the modulation of RhoGTPases. Results: We show that different concentrations of SDF-1aα modulate the balance of adhesion and migration in cancer cells. Increased migration was obtained at 50 and 100ng/ml of SDF-1aα however migration was reduced at 200ng/ml. The adhesion between breast cancer cells and BMHC was significantly increased by SDF-1aα treatment at 200ng/ml and reduced using a blocking monoclonal antibody against CXCR4. We showed that at low SDF-1aα concentration, RhoA was activated and overexpressed, while at high concentration Rac1 was promoting SDF-1aα mediating-cell adhesion. Conclusion: We conclude that SDF-1aα concentration modulates migration and adhesion of brebreast cancer cells, by controlling expression and activation of RhoGTPases.
| Original language | English |
|---|---|
| Article number | 569 |
| Journal | BMC Cancer |
| Volume | 15 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - 1 Aug 2015 |
| Externally published | Yes |
Keywords
- Breast cancer
- Metastasis
- SDF-1alpha
- Stromal cells
- Tumor microenvironment