Communication between lung tumors and bones contributes to tumor progression
Massachusetts General Hospital (MGH) investigators have identified a way in which a type of lung cancer co-opts a portion of the immune system to increase tumor progression. In the Dec. 1 issue of Science, the team from the MGH Center for Systems Biology describes a "crosstalk" between lung tumors and bone marrow, which leads to the generation of a type of immune cell that travels to the tumor and promotes its progression.
"Immune cells play critical roles in cancer. For example, we already know that T cells can eliminate tumors and be activated with immunotherapies. Tumors are home to diverse immune cell types, some of which remain much less explored than T cells and could also control cancer progression" says Mikael Pittet, PhD, director of the Cancer Immunology Program in the MGH Center for Systems Biology and senior author of the Science paper. "Myeloid cells are immune cells that are attracting attention because they can infiltrate a broad range of tumors. These cells include neutrophils and macrophages and seem to modulate key cancer-associated activities."
Recent research has suggested that tumor-infiltrating myeloid cells are initially produced in the bone marrow. For the current study the MGH team further explored whether bone marrow activity was altered in the presence of cancer in another part of the body, in this instance lung cancer. Their initial experiments found increased bone activity in two mouse models of a common form of lung cancer and in 70 lung cancer patients, even in absence of bone metastasis. Both the number and activity of osteoblasts – cells that produce and reshape bone tissue – were increased within the bone marrow of mice with lung tumors compared with cancer-free animals; and reducing the number of osteoblasts in mice not only limited neutrophil infiltration of tumors but also interrupted tumor progression.
Examination of tumor-associated neutrophils revealed two populations, which could be distinguished based on the expression of a protein called SiglecF. The accumulation of neutrophils expressing high levels of SiglecF, compared to other neutrophils, depended on the numbers of osteoblasts in the bones. And these SiglecFhigh neutrophils were found to promote cancer infiltration. The cells exhibited many functions associated with tumor progression; their presence within mouse tumors substantially accelerated cancer growth, and in human lung tumors, a SiglecFhigh neutrophil signature was associated with poor patient survival. A search for factors that could carry an activating signal from lung tumors to osteoblasts, inducing the production of SiglecFhigh neutrophils, revealed the molecule called sRAGE. This soluble factor was found at higher levels in the blood of animals with lung tumors, could increase the activation of osteoblasts and contributed to the maturation of neutrophils in cultured cells.
"Our findings indicate the existence of long-distance interactions between lung tumors and bones: lung tumors remotely activate osteoblasts, and those bone cells, in turn, shape immunity by supplying tumors with cancer-promoting neutrophils," says Pittet, who is an associate professor of Radiology at Harvard Medical School. "Since patients with many types of cancer have elevated levels of myeloisd cells in their blood, it's possible that other tumors could have a similar interaction with bone to increase myeloid cell production."
Pittet adds that this study "shows the importance of studying cancer as a systemic disease. Investigating how organs far from tumors contribute to cancer progression should lead us to ways of manipulating those systemic activities in therapy. We have started to study the complexity of myeloid responses to cancer and to identify molecular and cellular components that promote the disease. With the ultimate goal of improving patients' quality of life, we hope that modulating myeloid pathways will overcome some of the limitations of current treatment options."
Camilla Engblom, PhD, and Christina Pfirschke, PhD, of the MGH Center for Systems Biology, are co-lead authors of the Science paper. Additional co-authors include Ralph Weissleder, MD, PhD, MGH Center for Systems Biology; David Scadden, MD, MGH Center for Regenerative Medicine, Miriam Bredella, MD, MGH Department of Radiology; Marie Demay, MD, MGH Department of Medicine; Allon Klein, PhD, Harvard Medical School; and Richard Hynes, PhD, Massachusetts Institute of Technology. The study was supported in part by the Samana Cay MGH Research Scholar Fund, the Robert Wenner Award from the Swiss Cancer League, and National Institutes of Health grants R01-AI084880 and R01-CA206890.
Massachusetts General Hospital, founded in 1811, is the original and largest teaching hospital of Harvard Medical School. The MGH Research Institute conducts the largest hospital-based research program in the nation, with an annual research budget of more than $900 million and major research centers in HIV/AIDS, cardiovascular research, cancer, computational and integrative biology, cutaneous biology, genomic medicine, medical imaging, neurodegenerative disorders, regenerative medicine, reproductive biology, systems biology, photomedicine and transplantation biology. The MGH topped the 2015 Nature Index list of health care organizations publishing in leading scientific journals and earned the prestigious 2015 Foster G. McGaw Prize for Excellence in Community Service. In August 2017 the MGH was once again named to the Honor Roll in the U.S. News & World Report list of "America's Best Hospitals."