Stopping Breast Cancer Metastasis
Researchers from Huntsman Cancer Institute at the University of Utah in Salt Lake City have discovered a cellular mechanism that drives the spread of breast cancer to other parts of the body, as well as a therapy which blocks that metastasis. The research results were published online in the journal Cell Reports on January 2nd 2014.
A release from the university quotes senior author Alana Welm, PhD as saying, “Genetic mutations do not drive this mechanism. Instead, it’s improper regulation of when genes turn on and off.”
The new discovery focuses on a protein called RON kinase (RON), which signals some areas of tumor cell DNA to become active. Normally, RON operates mostly during embryonic development and is not highly expressed in healthy adults. But in about 50 percent of breast cancer cases, RON becomes re-expressed and reprograms genes responsible for metastasis, making them active.
“If there’s an entire program in the tumor cell that’s important for metastasis, blocking one small part of that program, for example, the action of a single gene, will probably not be an effective strategy,” Welm said. “But if you could find a way to turn off the entire program, you’re more likely to have the desired effect. We found that inhibiting RON turns off the entire metastasis program in these tumor cells. No one has ever described a specific pathway driving this kind of reprogramming in metastasis, much less a way to therapeutically block it. Also, RON has not previously been known to be involved in reprogramming gene expression.”
Future work will include investigating the potential of detecting the RON-dependent program in tumor cells as a way to identify patients that are more likely to develop metastases and as a predictor of therapeutic response to drugs that inhibit RON.