When a cancer cell sloughs off the edge of a tumor in the breast, it faces a tough road to survive. The cell must not only remain physically intact as it rushes through blood vessels, but it also must find a new organ to lodge itself in, take in enough nutrients and oxygen to stay alive, and begin dividing, all while escaping notice by the body's immune system.
A team of Howard Hughes Medical Institute (HHMI) scientists has discovered that some loose breast cancer cells, have a leg up on survival—the genes they express make them more likely to prosper in bone tissue. The team also found that whether or not cancer cells turn on those genes depends on what their surroundings were like in the primary breast tumor. If the breast tumor had molecular patterns similar to those found in bone, the tumor is more likely to spread to bone later.
"It's like in society -- who you hang out with shapes who you are," says HHMI investigator Joan Massagué of Memorial Sloan-Kettering Cancer Center. "And that might make you better or worse equipped to handle situations you'll encounter."
The new findings, published August 29, 2013 in the journal Cell, could eventually lead to new drugs that block cancers from spreading to bone or other organs, he says.
When cells from a primary tumor circulate through the body and begin growing in a new organ, a metastatic tumor is formed. Such metastases are often harder to treat than primary tumors; the vast majority of people who die of cancer have not only a primary tumor but also metastatic disease. So a major goal of cancer researchers is to not only find ways to treat primary tumors, but stop cancer from metastasizing.
Massagué's lab group discovered in 2009 that by looking at the genetics of breast cancer cells, they could predict which were most likely to spread to bone. A set of genes dubbed the Src response signature (SRS) was more often turned on in the cells that metastasized to the bone. But the researchers didn't know why.
"What was really a conundrum was how this pathway got turned on in the first place," says Massagué. "Because SRS didn't confer any survival benefit to cells in the primary tumor. We were really at a loss for clues."
So he and his colleagues took another look at breast tumors that had SRS turned on. They tested whether there were any other genes, outside the known SRS pathway, that were always turned up on down in the same cells. They homed in on two—CXCL12 and IGF1—that were not only found to be more highly expressed in tumors with SRS, but were also independently predictive of which tumors would migrate to the bone. Tumors with both genes turned up were more likely to lead to bone metastases.
But in the breast tumors with high levels of CXCL12 and IGF1, the researchers found, the genes weren't originating from cancer cells. Tumors consist of not only cancerous cells, but also other supporting cells that are integrated into the tumors' structure. The gene signature, it turned out, was coming from noncancerous mesenchymal cells integrating into the breast tumor. And not only that, but CXCL12 and IGF1 were also known to be expressed by bone cells. The genes, in both cases, encoded signaling molecules called cytokines.
"This was the eureka moment," says Massagué. "We realized there was mimicry between the environment of a primary tumor, and the environment of their preferred organ of metastasis."