Researchers have identified a novel genetic biomarker responsible for the progression of many breast and prostate cancers. The finding could bolster efforts to better identify patients who respond to certain types of chemotherapy drugs that attack the most aggressive forms of cancer. Their findings were published in Scientific Reports (2015; doi:10.1038/srep12136).

“Understanding and identifying biomarkers is a vital step toward cancer research and care,” said lead author Michael Freeman, PhD, vice chair of research in the Cedars-Sinai Department of Surgery in Los Angeles, California. “New profiling strategies exemplified by this study will ultimately improve our ability to treat cancer patients.”

The newly identified biomarker, diaphanous-related formin-3 or DIAPH3, participates in a protein interaction that makes cells rigid. The study found that when this biomarker is lost or lowered, cells become deformable, squeezing through tissue spaces, causing disease growth or progression. This phenomenon is known as an amoeboid phenotype.


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Researchers can utilize this knowledge to better identify patients who will respond to taxanes, common chemotherapy drugs typically given to patients with the most aggressive forms of cancer. The DIAPH3 protein network may indicate sensitivity to taxanes in human tumors. Taxanes work by damaging protein structures in cancer cells.

This is the first study to identify a targeting strategy for tumor cells that exhibit amoeboid properties.

“By identifying cancer biomarkers, then customizing treatment plans for individuals based on this genetic information, we can greatly improve the effectiveness of cancer therapies,” said Shlomo Melmed, MD, senior vice president of Academic Affairs and director of the Burns and Allen Research Institute. “This customized plan replaces a one-size-fits-all approach to cancer treatment.”

Next steps involve the development of a biomarker tool that will allow researchers to test these findings prospectively in patients.