Roughly 120 years ago, scientists predicted that bone tissue might manufacture certain molecules that entice cancer cells to lodge there. More people die of metastases -- secondary tumours that develop elsewhere in the body -- than from their initial tumours and bone is particularly fertile "soil" for travelling cancer "seed" cells. It has been estimated that 70 per cent of patients with progressive breast cancer and 84 per cent of prostate cancer patients develop bone metastases.
D. Holstead Jones, a former post-doctoral fellow in Professor Josef Penninger's laboratory of medical biophysics and immunology at U of T, is the lead author of the paper, which appears in the March 30 issue of the journal Nature. The team also included researchers from the University of Western Ontario's Department of Physiology and Pharmacology. Josef Penninger is currently the director of the IMBA in Vienna, where the project is being continued.
Jones and her colleagues show that RANKL, a cytokine protein which is produced at high levels in bone marrow, acts on breast, prostate and skin cancer cells through the RANK receptor. Over the past few years, Penninger's lab had determined that RANKL is essential in both bone breakdown and in controlling the growth of cells that form a lactating mammary gland. Putting these two discoveries together, the team decided to study the link between breast cancer and bone metastases and the RANKL system.
Jones and her colleagues studied bone metastases in a mouse model of skin melanoma, giving some animals a drug called osteoprotegerin (OPG), known to inhibit RANKL. "The mice that were treated with OPG had fewer tumours in their bones than the mice that were not treated," says Jones, now an assistant professor in the Faculty of Health Sciences at the University of Ontario Institute of Technology. For example, control mice showed migration of cancer cells into long bones, vertebrae, ovaries, adrenal glands and the brain and progressive tumour growth in control mice resulted in spinal cord invasion and subsequent paralysis. In mice treated with OPG, however, metastasis into bones and vertebrae was significantly reduced and none of the OPG-treated mice developed paralysis. The researchers noted that metastases into other organs were not slowed in OPG-treated mice.
Drugs that inhibit RANKL or its receptor might also block human metastases in bone, the researchers suggest. "Since there are novel inhibitors of RANKL far along in clinical development the idea is that people who have cancer that is known to spread to bone can start taking this drug when they are diagnosed," says Jones. "It would inhibit how much bone metastases they would have. Depending on the stage of cancer, it could be a preventive measure but it also may be something that would alleviate a lot of the pain that is produced by tumours within the bone."
"The findings are based on mouse studies and one always has to be careful to translate such studies to humans," cautions Penninger. However, the drug that blocks RANKL is already in late-stage clinical trials, meaning that it could be directly tested in humans with cancer in the near future. "Cancer metastases into bones are a huge problem. The estimate is that every year one million people develop metastases to the bones, in particular women with breast cancer," says Penninger. "The problem is that such metastases trigger severe cancer pain. With our findings we might not make people live longer but, if we are right, patients with cancer might have a much better quality of life."
The study was funded by the Canadian Institutes of Health Research, the Canadian Arthritis Network, the National Cancer Institute of Canada, IMBA, the Austrian National Bank, a European Union Marie Curie Excellence Grant and a European Union Marie Curie Mobility Fellowship.
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CONTACT:
D. Holstead Jones
University of Ontario Institute of Technology
905-721-3111 ext. 2539
Holly.JonesTaggart@uoit.ca
Josef Penninger
Institute of Molecular Biotechnology of the Austrian Academy of Sciences
University of Vienna
University of Toronto
011- 43-1-79044 ext. 4700
Josef.penninger@imba.oeaw.ac.at
Nicolle Wahl
U of T Public Affairs
416-978-6974
nicolle.wahl@utoronto.ca
Journal
Nature