New tissue-imaging technology could enable real-time diagnostics, map cancer progression

Simultaneous label-free autofluorescence multi-harmonic microscopy.

Illinois researchers developed a tissue-imaging microscope that can image living tissue in real time and molecular detail, allowing them to monitor tumors and their environments as cancer progresses. Image courtesy of Stephen Boppart

Illinois researchers have developed a new microscope system that holds the potential of capturing living tissue in real time and in molecular detail. The most fascinating is that it don’t require additional chemicals or dyes.

Using this system, scientists can easily study concurrent processes within cells and tissue. It can also mimic as a tool that provides insights on tumor progression.

Scientists named this microscope as simultaneous label-free autofluorescence multi-harmonic microscopy. It uses precisely tailored pulses of light to simultaneously image with multiple wavelengths.

SLAM microscopy follows a white blood cell called a leukocyte as it travels through a blood vessel.  Video courtesy of Stephen Boppart
SLAM microscopy follows a white blood cell called a leukocyte as it travels through a blood vessel.
Video courtesy of Stephen Boppart

The microscope is utilized on living tissue, even inside a living being, giving it the possibility to be utilized for clinical diagnosis or to control medical procedure in the working room. Second, it utilizes no colors or synthetic concoctions, just light.

In addition, the microscopy at the same time gathers different differentiations from cells and tissues, catching sub-atomic level points of interest and elements, for example, digestion.

During the study, scientists observed mammary tumors in rats, alongside the encompassing tissue condition. Because of the concurrent information, they could watch the range of dynamics as the tumors advanced and how different procedures interact.

Sixian You, the first author of the paper said, “We know the tumor is there, but tumors support a whole ecosystem in the tissue. They recruit healthy cells to support them. SLAM allows us to have a comprehensive picture of this ever-evolving tumor microenvironment at subcellular,  molecular and metabolic levels in living animals and human tissue. Monitoring that process can help us better understand cancer progression, and in the future could lead to better diagnosis of how advanced a tumor is, and better therapeutic approaches aimed at halting the progression.”

The researchers saw that the cells near the tumor had differences in metabolism and morphology, indicating that the cells had been recruited by cancer. In addition, they observed surrounding tissues creating an infrastructure to support the tumor, such as collagen and blood vessels. They also saw communication between the tumor cells and the surrounding cells in the form of vesicles, tiny transport packages released by cells and absorbed by other cells.

Now, scientists will use their technique to compare healthy tissue and cancer tissue in both rats and humans, focusing particularly on vesicle activity and how it relates to cancer aggressiveness. They are also working to make portable versions of the SLAM microscope that could be used clinically.

Dr. Stephen Boppart, a professor of bioengineering and electrical and computer engineering at Illinois and a medical doctor said, “There is a wealth of new data, information, and biomarkers in the images we collect from fresh tissue that is still metabolically active, or in living organisms, where we can visualize the dynamics of individual cells and their collective behaviors.”

” These, we expect, will become new markers for diseases such as cancer, and our imaging technology will help detect these for disease screening, diagnostics, and monitoring applications. We believe that this technology will open the possibility of complementing, or even replacing, standard histopathology processing, which is time- and labor-intensive and can only be done on removed, fixed, dead tissue.”

Scientists detailed their technique in the journal Nature Communications.