Studies Reveal More Clues on How Pregnancy Protects Against Breast Cancer

SAN DIEGO, CA (April 7, 2014)—Scientists at Fox Chase Cancer Center have unearthed new clues about how pregnancy reduces women's risk of developing breast cancer. The research will be presented at the AACR Annual Meeting 2014.

Taking a detailed look at the genetic material of women who had and had not given birth, the researchers noted differences in elements related to key processes that, when they go awry, can increase the risk of developing cancer.

Ideally, researchers will one day be able to mimic these changes in women who have not been pregnant in order to reduce their risk of developing cancer, says study author Julia Santucci-Pereira, PhD, Research Associate in the Breast Cancer Research Laboratory at Fox Chase.

"We are trying to understand how the natural process of giving birth helps prevent cancer," she says. "If we understand it, we can try to mimic this process somehow, especially in women who are at high risk of developing the disease."

In one study, that will be presented on the afternoon of Monday, April 7, Santucci-Pereira and her colleagues used sophisticated sequencing technology to compare the genetic activity of cancer-free breast tissue samples from more than 100 premenopausal women—30 of whom had never given birth. They spotted differences in the expression of genes that were associated with the process cells undergo to become specialized types, known as differentiation. This isn't a surprise, says Santucci-Pereira, since problems in differentiation can cause cells to become cancerous.

In addition, she and her colleagues noticed clear differences between mothers and non-mothers in the expression of genes related to the development of breast anatomy. This, too, makes sense, says Santucci-Pereira, as this process must be well regulated in order to avoid cancer.

In another study presented during the same session, Santucci-Pereira and her team identify additional genetic changes that may help explain how pregnancy protects against breast cancer. Looking at 10 women who had undergone menopause, they found that mothers and non-mothers displayed differences in how their genes were modified— specifically, by being tagged with chemical groups, which influences how those genes are used by the body. Here, again, they found differences in processes associated with the development of breast anatomy.

“Although this research brings scientists closer to understanding why pregnancy protects the body from cancer, how that happens remains a puzzle,” says Santucci-Pereira. One possibility, she says, is that the hormone produced during pregnancy—human chorionic gonadotropin (HCG)—induces these changes. Indeed, previous research in animals and human cells has found that adding HCG can produce other genetic changes tied to differentiation and development; study author Jose Russo, MD, who heads the Breast Cancer Research Laboratory at Fox Chase, is continuing to study HCG's effects on cancer. "We're trying to mimic pregnancy without making women get pregnant," says Santucci-Pereira.

Finally, in another study that will be presented on the morning of Monday, April 7, Santucci-Pereira and other scientists at Fox Chase looked deeply at differences in stretches of genetic material dubbed "non-coding," meaning they do not contain instructions for making protein. These are regions scientists once thought were "useless," says Santucci-Pereira, but now realize they interact with other parts of the genome and enhance their function. The next step is to try to understand what these non-coding regions actually do, including their role in cancer. "This is a very new field."

In the latest study, Santucci-Pereira and her colleagues identified 42 differences in non-coding regions between 8 mothers and 8 non-mothers. It's possible, she says, that these non-coding regions work with the genes identified in the other two studies to induce changes in the differentiation and development processes, thereby protecting women who have given birth.

Like with the other research, the goal is to find ways that mimic these effects in non-mothers—perhaps by administering compounds that target non-coding regions—they experience the same protection against breast cancer, says Santucci-Pereira. "There are ways, molecularly, to target non-coding regions," she says. "We are just trying to figure out how that would work."

Santucci-Pereira and Russo's co-authors on the gene expression research include Eric A. Ross, Michael Slifker, Suraj Peri, Ricardo López de Cicco, Yubo Zhai, Irma H. Russo, Theresa Nguyen, and Fathima Sheriff from Fox Chase, as well as researchers from New York University and Sunderby Hospital and Umeå University in Sweden. For the other studies, they were joined by Colleen O’Malley, Maria Barton of Fox Chase and researchers at the University of Texas Health Science Center.

Fox Chase Cancer Center (Fox Chase), which includes the Institute for Cancer Research and the American Oncologic Hospital and is a part of Temple Health, is one of the leading comprehensive cancer centers in the United States. Founded in 1904 in Philadelphia as one of the nation’s first cancer hospitals, Fox Chase was also among the first institutions to be designated a National Cancer Institute Comprehensive Cancer Center in 1974. Fox Chase is also one of just 10 members of the Alliance of Dedicated Cancer Centers. Fox Chase researchers have won the highest awards in their fields, including two Nobel Prizes. Fox Chase physicians are also routinely recognized in national rankings, and the Center’s nursing program has received the Magnet recognition for excellence six consecutive times. Today, Fox Chase conducts a broad array of nationally competitive basic, translational, and clinical research, with special programs in cancer prevention, detection, survivorship, and community outreach. It is the policy of Fox Chase Cancer Center that there shall be no exclusion from, or participation in, and no one denied the benefits of, the delivery of quality medical care on the basis of race, ethnicity, religion, sexual orientation, gender, gender identity/expression, disability, age, ancestry, color, national origin, physical ability, level of education, or source of payment.

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