Early Changes Leading to Breast Tumors Revealed by Spectroscopic Imaging
By MedImaging International staff writers
Posted on 26 Mar 2012
Researchers have created a new imaging technology that reveals slight changes in breast tissue, representing a potential tool to determine a woman’s risk of developing breast cancer and to assess ways of preventing the disease. Posted on 26 Mar 2012
The researchers, using a special three-dimensional (3D) culture that mimics living mammary gland tissue, also showed that a fatty acid found in some foods influences this early precancerous stage. Unlike traditional cell cultures, which are flat, the 3D cultures have the round shape of milk-producing glands and behave like real tissue, according to Dr. Sophie Lelièvre an associate professor of basic medical sciences at Purdue University (West Lafayette, IN, USA).
Researchers are studying changes that take place in epithelial cells, which make up tissues and organs where 90% of cancers occur. The changes in breast tissue are thought to be necessary for tumors to form, she said. “By mimicking the early stage conducive to tumors and using a new imaging tool, our goal is to be able to measure this change and then take steps to prevent it,” Dr. Lelièvre said.
The new imaging technique, called vibrational spectral microscopy, can be used to identify and track certain molecules by measuring their vibration with a laser. Whereas other imaging tools may take days to get results, the new method works at high speed, enabling researchers to measure changes in real time in live tissue, according to Dr. Ji-Xin Cheng, an associate professor of biomedical engineering and chemistry. By monitoring the same three-dimensional (3D) culture before and after exposure to certain risk factors, the new method enables researchers to detect subtle changes in single live cells, he reported.
Findings are detailed in a research paper that appeared March 7, 2012, in the Biophysical Journal. The article was written by doctoral students Shuhua Yue, Juan Manuel Cárdenas-Mora, and Lesley S. Chaboub, Lelièvre and Dr. Cheng. “This work shows the importance of engineering for the development of primary prevention research in breast cancer,” said Mr. Yue, a biomedical engineering student whose work was funded through a fellowship from the US Department of Defense Breast Cancer Research Program.
Researchers evaluated live tissue in a culture that reproduces the mammary epithelium. “This extremely sensitive technique shows the harmful impact of a nutrient called arachidonic acid,” said Dr. Lelièvre, associate director of discovery groups at the Purdue Center for Cancer Research. “This fatty acid has been previously proposed to increase breast cancer risk, but until now there was no biological evidence of what it could do to alter breast epithelial cells."
The imaging method identifies changes in the “basoapical polarity” of epithelial tissues. Specific proteins and other biochemical compounds called lipids are typically located in one of two regions, called the basal and apical membranes. Because only specific proteins and lipids are found in basal membranes, while others are located only in apical membranes, the cells are reported to be polarized.
“This polarity is critical for the proper structure and function of tissue,” Dr. Lelièvre said. “What we have shown previously is that when polarity is altered, tissue that otherwise looks normal can be pushed into a cell cycle necessary to form a tumor. It’s the earliest change in the epithelial tissue that puts the cells at risk to form a tumor. Now, thanks to the vibrational spectral microscopy technique developed by Dr. Cheng, we can measure apical polarity status in live tissues and real time.”
The findings could lead to a way to prevent tumor formation by restoring the correct polarity. “We are mimicking formation of breast epithelium as it is normally polarized, and we can play with it and make it lose apical polarity on demand,” Dr. Lelièvre said. “Then we can mimic an early change thought to be conducive to tumor development.”
The researchers’ goal is to use the imaging technology on live 3D cultures of noncancerous breast tissue to screen for protective and risk factors for breast cancer the same way that tumors are used now in cultures to screen for drugs that can be used for treatment. “Now there is no good way to assess risk for breast cancer,” Dr. Lelièvre said. “Assessments are mainly based on family history and genetic changes, and this only accounts for a very small percentage of women who get breast cancer. We need technologies to assess the risk better and then screen for protective factors that could be used on individual patients because not everybody will be responsive to the same factors.”
An immediate application of the technique is a way to study cell lines created from tissue taken from women at different risk levels, screening for factors that could restore full polarity in the breast tissue to prevent tumor formation. “The state of the art is to take tumor cells, put them in a 3D culture where they form tumors, and then test drugs on these tumors,” Dr. Lelièvre said. “What we want to do now is the same thing but for preventive strategies using a normal tissue.”
In a collaboration with researchers at Indiana University-Purdue University Indianapolis, the team plans to study cell lines from women who are at different risk levels. The new imaging tool was needed because traditional live cell imaging methods are designed for flat cell cultures. Mimicking tissue polarity requires a 3D culture to form the mammary gland structures at the end of the breast ducts. The structures resemble tiny balls about 30 micrometers in diameter and contain approximately 35 cells.
Dr. Cheng reported that his lab will continue to develop a “hyperspectral” imaging system capable of not only imaging a specific area in a culture but also many locations to form a point-by-point map so that tissue polarity can be directly visualized.
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