Breast Cancer Metastasis Linked to the Structural Protein Palladin

They found that the ability to migrate through the tissue membrane depended on the cell's level of palladin expression. Palladin was expressed at higher overall levels in tumors compared with benign breast tissue, and was expressed significantly higher in four invasive breast cancer cell lines than in the non-invasive cells lines. Additionally, they found that palladin played a key role in the formation of podosomes, actin-rich structures that function in adhesion and matrix degradation, and have been found in many invasive cell types.

Cells that had been genetically engineered to lack the gene for palladin demonstrated decreased podosome formation and a significant reduction in migration and invasive motility. Palladin overexpression induced podosome formation in non-invasive MCF7 cells, which were otherwise unable to form podosomes, suggesting that palladin played a critical role in the assembly of podosomes.

"This study shows that palladin may play an important role in the metastasis of breast cancer cells as they move out of the tumor and into the blood vessels and lymphatics to spread throughout the body,” said senior author Dr. Carol Otey, associate professor of cell and molecular physiology at the University of North Carolina. "To really make breast cancer a treatable disease, we have to be able to find a way to prevent or reduce the amount of metastasis. Now that we see palladin is expressed mostly in invasive cells, it raises the question as to whether it might be useful as a prognostic marker. Maybe someday doctors could test for the presence of palladin to identify patients who have the most aggressive tumors, then give those patients personalized, more aggressive treatment.”

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