Immune System May Impact Tumor Blood Supply
December 15, 2010
· Early research suggests that the immune system can affect angiogenesis.
· Manipulation of angiogenesis is a key therapeutic strategy for cancer.
PHILADELPHIA — Scientists at the Dana-Farber Cancer Institute may have uncovered a mechanism for blocking tumor angiogenesis that involves the patient’s immune system, according to findings published in Cancer Research, a journal of the American Association for Cancer Research.
Angiogenesis is the process by which tumors acquire and process blood, which is needed for their continued growth. Anti-angiogenesis drugs block blood flow and are an important part of cancer treatment.
“Substantial evidence indicates that inhibiting angiogenesis is a validated strategy for cancer therapy, but current approaches are in need of further improvements,” said Glenn Dranoff, M.D., associate professor of medicine at the Dana-Farber Cancer Institute.
Dranoff and colleagues analyzed blood and tumor samples from patients who showed clinical responses to treatment with a combination of immune stimulants and regulatory molecules. Unexpectedly, the study showed that these immunotherapies stimulated a host response that targeted the selective destruction of tumor blood vessels. A key step in this process was the ability of patients to generate antibodies that neutralized factors that produce and sustain tumor blood vessels.
Overall, the immune treatments activated cellular processes in the tumor microenvironment that achieved an anti-angiogenic response.
“It appears that the body’s own immune system can be used to develop a new way to block angiogenesis,” said Dranoff. “Angiogenesis involves multiple factors, and our studies suggest that it may be advantageous to target several of these at the same time, rather than only focus on one factor, such as vascular endothelial growth factor.”
Mark Smyth, Ph.D., head of the Cancer Immunology Program at Peter MacCallum Cancer Center in Australia, and a section editor of Cancer Research, believes this research represents important new information in the angiogenesis arena.
“It has long been recognized that anti-angiogenesis is a worthwhile therapeutic approach to cancer treatment and a number of molecules have been defined as potential targets,” said Smyth.
“The important issue here is that combination therapy does, in fact, raise host antibodies to these angiogenic targets. Future efforts to generate immunotherapies to cancer need to keep this information in mind.”
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The mission of the American Association for Cancer Research is to prevent and cure cancer. Founded in 1907, the AACR is the world’s oldest and largest professional organization dedicated to advancing cancer research. The membership includes 33,000 basic, translational and clinical researchers; health care professionals; and cancer survivors and advocates in the United States and more than 90 other countries. The AACR marshals the full spectrum of expertise from the cancer community to accelerate progress in the prevention, diagnosis and treatment of cancer through high-quality scientific and educational programs. It funds innovative, meritorious research grants, research fellowships and career development awards. The AACR Annual Meeting attracts more than 18,000 participants who share the latest discoveries and developments in the field. Special conferences throughout the year present novel data across a wide variety of topics in cancer research, treatment and patient care. Including Cancer Discovery, the AACR publishes seven major peer-reviewed journals: Cancer Research; Clinical Cancer Research; Molecular Cancer Therapeutics; Molecular Cancer Research; Cancer Epidemiology, Biomarkers & Prevention; and Cancer Prevention Research. AACR journals represented 20 percent of the market share of total citations in 2009. The AACR also publishes CR, a magazine for cancer survivors and their families, patient advocates, physicians and scientists.