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Promising new therapeutic target for aggressive breast cancer

Date:
August 1, 2012
Source:
University of Western Ontario
Summary:
Scientists have identified a new therapeutic target for advanced breast cancer which has shown tremendous promise in mouse models. The study looked at a protein called Nodal that is primarily found in embryonic or stem cells. Researchers discovered high levels of this protein in aggressive breast cancer tumors.
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Scientists at Western have identified a new therapeutic target for advanced breast cancer, which has shown tremendous promise in mouse models.

The study, led by Lynne-Marie Postovit of Western's Schulich School of Medicine & Dentistry, looked at a protein called Nodal that is primarily found in embryonic or stem cells. Postovit discovered high levels of this protein in aggressive breast cancer tumors. Nodal was found to promote vascularization in the tumor, providing nutrients and oxygen to help it grow and spread.

The research is published online in the journal Cancer Research.

"We have determined that breast cancers, specifically those very aggressive, invasive breast cancers that spread, express an embryonic protein called Nodal and the expression of this protein is correlated with more blood vessels in the tumor," said Postovit, of the Department of Anatomy and Cell Biology. "Blood vessels, many studies have shown, help to allow tumors to grow but also to spread throughout the body.

In addition, we have shown that if we can target this embryonic protein, we can cause the blood vessels to collapse within the tumor, leading to decreased oxygen levels and tumor cell death. When tumors lack oxygen and nutrients they become what we call necrotic."

In the study, mouse models were designed to develop breast cancer tumors. Researchers then turned off the expression of Nodal using a genetic modification. When they did that, the blood vessels in the tumor appeared to collapse, and the tumor was less aggressive.

Nodal is on the outside of the cell, so it can be easily targeted by a number of mechanisms including antibodies. Since Nodal isn't expressed in normal tissue in the body, it would be possible to target just the cancer, allowing for better patient outcomes.

"Ultimately it would be nice to target Nodal in patients who already have quite advanced, well-vascularized tumors as a new option for therapy," said Daniela Quail, first author on the research and a PhD candidate in Postovit's lab. "Currently, patients like this don't have many options."

"In Canada, breast cancer continues to be one of the most common forms of cancer in women. Although new treatment methods have improved outcomes, a significant number of women still die from this disease," added Morag Park, Scientific Director of the Canadian Institutes of Health Research. "Research advancements, such as Dr. Postovit's, have contributed and will continue to contribute to the improvements around our understanding of cancer progression and treatment."

The research was funded by the Canadian Institutes of Health Research, the Cancer Research Society and the Canadian Breast Cancer Foundation.


Story Source:

Materials provided by University of Western Ontario. Note: Content may be edited for style and length.


Journal Reference:

  1. D. F. Quail, L. A. Walsh, G. Zhang, S. D. Findlay, J. Moreno, L. Fung, A. Ablack, J. D. Lewis, S. J. Done, D. A. Hess, L.-M. Postovit. Embryonic Protein Nodal Promotes Breast Cancer Vascularization. Cancer Research, 2012; 72 (15): 3851 DOI: 10.1158/0008-5472.CAN-11-3951

Cite This Page:

University of Western Ontario. "Promising new therapeutic target for aggressive breast cancer." ScienceDaily. ScienceDaily, 1 August 2012. <www.sciencedaily.com/releases/2012/08/120801093823.htm>.
University of Western Ontario. (2012, August 1). Promising new therapeutic target for aggressive breast cancer. ScienceDaily. Retrieved April 19, 2024 from www.sciencedaily.com/releases/2012/08/120801093823.htm
University of Western Ontario. "Promising new therapeutic target for aggressive breast cancer." ScienceDaily. www.sciencedaily.com/releases/2012/08/120801093823.htm (accessed April 19, 2024).

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