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Breast cancer growth signals are enhanced by a protein outside cells

New research uncovers how a sticky protein called fibronectin promotes the activity of oestrogen in breast cancer cells.

The study, "Fibronectin rescues estrogen receptor α from lysosomal degradation in breast cancer cells," which was published July 6 in the Journal of Cell Biology (JCB), was led by Rocío Sampayo, a PhD student in Dr. Marina Simian's lab at the Instituto de Nanosistemas, Universidad Nacional de San Martin and Instituto "Ángel H. Roffo," Universidad de Buenos Aires in Argentina.

Together they show a novel mechanism of oestrogen receptor signalling that is regulated by fibronectin.

They found that exposure to fibronectin prolongs the activity of oestrogen receptors in breast cancer cells.

The hormone oestrogen plays a key role in the development of healthy cells and, in many cases, cancerous cells.

Oestrogen attaches to cellular oestrogen receptors, which promote cell growth and survival.

But too much oestrogen receptor activity can cause cells to proliferate rapidly, leading to tumour growth.

About 75% of breast cancers are considered oestrogen receptor positive because oestrogen causes those cancers to propagate, Sampayo notes.

As cancerous cells start to invade into surrounding tissue, they encounter the gluey fibronectin protein.

"In the normal mammary gland, epithelial cells are not in contact with fibronectin," Sampayo explains.

Fibronectin is part of the extracellular matrix, the meshwork of proteins and molecules that surrounds cells.

In tumours, the production of this surrounding network often becomes unregulated.

Previous research has shown that high levels of fibronectin and its receptor β1-integrin correlate with lower breast cancer survival, but it was not known why.

In the current study, Sampayo and colleagues discovered that fibronectin boosts oestrogen receptors' activity in breast cancer cells.

They found that when breast cancer cells are surrounded by fibronectin, oestrogen receptors avoid destruction by lysosomes--cellular garbage disposal units--and can continue to drive cancer cell growth.

"This would allow breast cancer cells to become resistant to common endocrine therapy drugs that target the receptor," Sampayo says.

Their research suggests that therapeutics that interfere with fibronectin's influence on the oestrogen receptor could help treat drug-resistant breast cancers.

This work also reveals how the meshwork of proteins surrounding tumours can influence cancer progression.

Source: The Rockefeller University Press



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