Cancer Biology, Cell Biology
Memorial Sloan-Kettering Cancer Center
Dr. Massagué holds the Alfred P. Sloan Chair in the Cancer Biology and Genetics Program at Memorial Sloan-Kettering Cancer Center. He is also a professor at the Weill-Cornell Graduate School of Medical Sciences.
Joan Massagué is interested in the mechanisms that support tissue homeostasis and cancer metastasis. Focusing on transforming growth factor-β (TGFβ) as one of the most prevalent signaling pathways in metazoan biology, he elucidated this signaling pathway and is establishing how TGFβ signals control pluripotency and differentiation in stem cell and homeostasis in mature cells. He is also interested in how cancer cells co-opt this and other pathways for metastases. His goal is to use this basic knowledge for treating cancer.
Over the past 30 years, our understanding of the birth and growth of tumor cells has expanded dramatically. Much less is known about metastasis, which enables cells to leave the primary tumor and spawn new tumors elsewhere. What surprises Joan Massagué is the lengths to which tumor cells go to take over the body. But he is determined to beat cancer at its own game.
Massagué became interested in human health while growing up in Barcelona. "But I didn't see myself as a physician," he says, "but as someone who wants to understand how diseases occur based on mishaps in physiology."
While studying insulin's action at the University of Barcelona and, later, at the University of Massachusetts, Massagué's interest strayed to a class of growth factors called transforming growth factor-betas (TGFβs). "These factors have a profound influence on how cells go about the business of organizing themselves into tissues and organs," he says, adding that failure to obey their commands can transform normal cells into cancer.
Massagué emigrated to the United States in 1979, and by 1983 he had isolated TGFβ from tumor cells. He then began to document that factor's many effects on cells, and identified and purified its multipart receptor.
By 1994, his group had discovered how TGFβ activates that receptor. The same year, he and his collaborators showed that activating one arm of the TGFβ pathway keeps cells from dividing. This explained why cells can become malignant when that arm of the pathway stops working, because tumors arise when cells proliferate unrestrainedly.
The researchers soon filled in the blanks between the beginning and end of the TGFβ pathway and discovered proteins that commute into the nucleus to convey its inhibitory signal. Massagué derived a lot of satisfaction from this project because it usually takes many groups to accomplish such an undertaking. "Although I was trained as a biochemist," he says, "what really interests me is how a biological process works in its entirety."
The researchers later showed that cancer cells use various tricks to disable the TGF pathway's growth-inhibiting arm. But why go to the trouble when it would be simpler to disable the receptor, as colon cancer cells do? Further experiments showed that cancer cells that keep the receptor intact and just rid themselves of the pathway's growth-inhibitory arm are free to co-opt other arms to do their dirty work. "This was a wild moment for me," Massagué recalls. "It inspired me to study metastasis as a whole."
It was known that another arm of the TGF pathway boosts the production of a protein called interleukin-11 in mammary cells. When such cells are transformed and metastasize to bone, they are hemmed in by hard tissue. But bone is awash with TGFβ, which can no longer keep these breast cells under control. Massagué found that the cancer cells use TGF to their own advantage because the interleukin-11 it helps them secrete recruits osteoclasts—the cells that chew up bone. By riddling bone with holes, the cancer cells create living space for themselves. "That was a real eye opener in terms of how complex and perverse the problem of metastasis really is," Massagué says.
In 2005, the researchers reported that a quartet of genes causes primary breast tumors to grow more blood vessels, which in turn promote tumor growth. The vessels, being highly permeable, also provide an easy escape route for the tumor cells. When the emigrants arrive in the lungs, they use the same four genes to pass from blood capillaries into lung tissue, where they spawn new tumors. "So a set of four genes has been selected for being very useful at three very important and very limiting steps of the metastatic process," Massagué says.
Fortuitously, drugs that suppress the products of two of those genes are already on the market. Cetuximab is used to treat colorectal cancer, and celecoxib is used for inflammation. "We realized that if a cell resorts to the combination of the metastatic genes, maybe metastasis could be suppressed by the combination of drugs that blocks the products of those genes," Massagué explains. When the researchers implanted mammary tumors into mice and gave the animals cetuximab and celecoxib at the same time, the mice developed 10- to 20-times fewer tumors in the lung than implanted but untreated mice.
Until a few years ago, preclinical discoveries took decades to benefit patients. But Massagué has already started discussions with oncologists about the best way to launch clinical trials with the cetuximab/celecoxib combination. "The speed with which we are accruing answers to questions with clinical relevance has been much faster than I ever anticipated," he says.