Cancer cells can now be spotted accurately with a new imaging technique that uses laser light to identify cancer cells.
The research team demonstrated the novel microscopy technique, called nonlinear interferometric vibrational imaging (NIVI), on rat breast-cancer cells and tissues. It produced easy-to-read, color-coded images of tissue, outlining clear tumor boundaries, with more than 99 percent confidence - in less than five minutes.
AdvertisementThe research was led by professor and physician Stephen A. Boppart,.
In addition to taking a day or more for results, current diagnostic methods are subjective, based on visual interpretations of cell shape and structure. A small sample of suspect tissue is taken from a patient, and a stain is added to make certain features of the cells easier to see. A pathologist looks at the sample under a microscope to see if the cells look unusual, often consulting other pathologists to confirm a diagnosis.
"The diagnosis is made based on very subjective interpretation - how the cells are laid out, the structure, the morphology," said Boppart, who is also affiliated with the university's Beckman Institute for Advanced Science and Technology.
"This is what we call the gold standard for diagnosis. We want to make the process of medical diagnostics more quantitative and more rapid."
Rather than focus on cell and tissue structure, NIVI assesses and constructs images based on molecular composition. Normal cells have high concentrations of lipids, but cancerous cells produce more protein. By identifying cells with abnormally high protein concentrations, the researchers could accurately differentiate between tumors and healthy tissue - without waiting for stain to set in.
Each type of molecule has a unique vibrational state of energy in its bonds. When the resonance of that vibration is enhanced, it can produce a signal that can be used to identify cells with high concentrations of that molecule. NIVI uses two beams of light to excite molecules in a tissue sample.
"The analogy is like pushing someone on a swing. If you push at the right time point, the person on the swing will go higher and higher. If you don't push at the right point in the swing, the person stops," Boppart said.
"If we use the right optical frequencies to excite these vibrational states, we can enhance the resonance and the signal."
One of NIVI's two beams of light acts as a reference, so that combining that beam with the signal produced by the excited sample cancels out background noise and isolates the molecular signal. Statistical analysis of the resulting spectrum produces a color-coded image at each point in the tissue: blue for normal cells, red for cancer.
Another advantage of the NIVI technique is more exact mapping of tumor boundaries, a murky area for many pathologists. The margin of uncertainty in visual diagnosis can be a wide area of tissue as pathologists struggle to discern where a tumor ends and normal tissue begins. The red-blue color coding shows an uncertain boundary zone of about 100 microns - merely a cell or two.
"Sometimes it's very hard to tell visually whether a cell is normal or abnormal," Boppart said. "But molecularly, there are fairly clear signatures."
The findings will be published in the journal Cancer Research.