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FOR IMMEDIATE RELEASE: October 14, 2009


CONTACT:

Karen Mallet (media only)
215-514-9751
km463@georgetown.edu


Gene blamed for immunological disorders shown to protect against breast cancer development

Researchers say the findings suggest drug therapy targeted against the gene’s protein may be risky


Washington, DC – Researchers at the Lombardi Comprehensive Cancer Center at Georgetown are voicing alarm that drugs to treat a wide variety of allergies, asthma and autoimmune diseases now in human clinical trials may errantly spur development of breast tumors.

As the researchers report in the October 15 issue of PLoS ONE, the gene SYK and its protein product, Syk*, are crucial for prevention of breast cancer in the mice and human breast cells they studied. The research is the most definitive yet to demonstrate the beneficial function of Syk as a tumor suppressor, but Syk is better known for its negative role in ramping up activity of the immune system, leading to a cornucopia of immunological disorders.

The concern the authors have is that agents for these conditions – which are now being tested in humans – might spur breast cancer development because they are designed to inhibit the activity of Syk. “Our study shows that in normal breast cells, Syk is needed to control growth and thus prevent breast cancer. So if people use a drug that stops Syk activity, they could be at risk for developing this cancer, particularly at a young age during breast development” says the study’s senior author, Susette Mueller, PhD, professor of oncology at Lombardi.

“Years of research has led us to believe that Syk is important in breast cancer, but we still need to find out why and when some women lose Syk function,” she says. “In the meantime, we can only voice concern that inhibiting the protein may have unfortunate consequences.”

She adds that Syk is a complex gene product, and that researchers elsewhere have also shown that it can promote development of other types of cancer, such as head and neck and certain forms of leukemia. “As we are discovering more and more, proteins can have different functions in the human body, depending on the context in which they are used. Syk is a perfect example of this phenomenon,” Mueller says.

Mueller and her collaborators have been studying Syk for about a decade, and have the largest body of work detailing how it functions in the breast. They first showed that Syk protein is present in normal breast cells and its absence correlated with invasion and metastasis in tumor cells and later found that as breast tumors progressed, more and more Syk protein was lost. Now, it is recognized that the amount of Syk present in a tumor is an indicator of risk of metastasis.

In this study, first author You Me Sung, PhD, a postdoctoral researcher in Mueller’s lab, conducted mice studies in which one of two Syk alleles were genetically deleted. (Because Syk is believed to be important in embryonic development as well, deleting both will not sustain life.) The research team demonstrated that loss of the single allele led to “profoundly” increased proliferation and invasion of normal breast cells in the mouse mammary gland during puberty, resulting in development of breast cancer in adulthood. They then studied normal human breast cells in laboratory culture, and showed that knocking out Syk protein dramatically increased cell growth as well, and produced changes that would allow cells to invade through tissue-like barriers.

“Our findings in living mouse and in human breast cells mirrored each other,” Mueller says. “All the data on Syk suggest it is very important in controlling growth as breast tissue develops indicating a potent role as tumor suppressor for breast cancer.”

The researchers are now studying patients who have lost Syk function in order to pinpoint the reason why the gene no longer produces its protein. Ultimately, the goal is to identify the molecules that Syk negatively regulates in order to target them for breast cancer therapy.

The study was funded by the National Institutes of Health and by a postdoctoral research fellowship from the Susan G. Komen Breast Cancer Fellowship. The authors declare no related financial interests.

*Note to editor: When referring to the gene, SYK is written in all caps. The protein is written Syk.

About the Georgetown Lombardi Comprehensive Cancer Center
The Lombardi Comprehensive Cancer Center, part of Georgetown University Medical Center and Georgetown University Hospital, seeks to improve the diagnosis, treatment and prevention of cancer through innovative basic and clinical research, patient care, community education and outreach, and the training of cancer specialists of the future. Lombardi is one of only 40 comprehensive cancer centers in the nation, as designated by the National Cancer Institute, and the only one in the Washington, DC, area. For more information, go to http://lombardi.georgetown.edu.

About Georgetown University Medical Center
Georgetown University Medical Center is an internationally recognized academic medical center with a three-part mission of research, teaching and patient care (through our partnership with MedStar Health). Our mission is carried out with a strong emphasis on public service and a dedication to the Catholic, Jesuit principle of cura personalis -- or "care of the whole person." The Medical Center includes the School of Medicine and the School of Nursing and Health Studies, both nationally ranked, the world-renowned Lombardi Comprehensive Cancer Center and the Biomedical Graduate Research Organization (BGRO), home to 60 percent of the university’s sponsored research funding.
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