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Monday, 3 March 2014

Myoferlin, a protein only recently linked to cancer, may help breast cancer cells transform so they can escape tumors and migrate to new sites. When researchers implanted mice with breast cancer cells that couldn't make the protein because of its gene was switched off, the cells did not transform into the type that migrates.
Researchers at The Ohio State University (OSU) in Columbus, had already shown this was happening in cell cultures. Now in a study published in the journal PLOS ONE, they describe how they got similar results in mice.
The mice implanted with breast cancer cells lacking the ability to make myoferlin developed small, self-contained tumors that only contained non-migrating cells.
But mice implanted with breast cancer cells that could make myoferlin developed larger, irregular tumors whose cells invaded surrounding tissue.
In their study report the researchers describe how they found two main effects from reducing cancer cells' ability to make myoferlin: one affected behavior of the cells, and the other their mechanical properties.
It appears that without myoferlin, many genes required to help cells migrate (metastasize) don't get switched on, so they behave more like cells that stay put.
And without myoferlin, the cells can't alter the mechanical properties that make it possible for them to travel and invade. Instead, they stay huddled together in the primary tumor.

Findings open door to possible new individualized treatments

These and other findings mean it may be possible to develop breast cancer treatment tailored to an individual's need - depending on the protein levels and mechanical properties of their breast cancer cells.
Senior author Douglas Kniss, professor of obstetrics and gynecology at OSU's Wexner Medical Center, explains how their discoveries may be useful:
Read more on: http://www.medicalnewstoday.com/articles/273442.php

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