Stanford researchers have developed a molecular probe that lights up tumour cells in animals, improving diagnosis and treatment of cancer and other diseases.
The probe's main ingredient is a molecule that labels active proteases, which are protein-destroying enzymes that run in cancerous cells. The molecule is usually invisible to the naked eye but it has a fluorescent tag that glows when it binds to the protease. The tag sends out near-infrared light that passes through skin and is detectable with a special camera.
"Nowadays the detection of cancer, breast cancer for instance, is normally done by mammography, using X-rays - which might actually increase your risk of cancer. We think these probes may ultimately provide a less harmful, non-invasive method of detecting cancer," said the article's lead author Galia Blum, PhD, a postdoctoral scholar in the laboratory of Matthew Bogyo, PhD, assistant professor of pathology.
A key advantage of this enzyme-targeting molecule is its size. About 100 times smaller than other molecular imaging reporters, it can easily slip across the cell membrane and enter living cells. It can also move through the animal quickly, which opens up the possibility of using the technique to light up tumours while surgery is in progress.
"Unlike other enzyme-targeting molecules, it's very specific, sticks to where it binds and does it all very rapidly - in 30 minutes or less," Bogyo said.
And unlike most other molecular probes, this type identifies only active enzymes.
"We went one step beyond just telling if the enzymes are there. We can answer the question, 'Are they active'. That's important because an accumulation of inactive enzymes doesn't necessarily indicate disease," Blum said.
Bogyo, Blum and colleagues designed the probe to bind to a subset of a family of proteases called cysteine cathepsins, which are more active in several types of cancer as well as other diseases. Now they are tinkering with the probe's configuration in an effort to create a variant that recognizes the enzymes involved in apoptosis, the process of cell death.
This could ultimately allow researchers and doctors to visualize response to chemotherapy in tumours, Bogyo said.
And because other diseases besides cancer involve hyped-up proteases - such as Alzheimer's, arthritis, atherosclerosis and osteoporosis - the approach might be of use in diagnosing and treating them as well.
In addition to the potential health-care applications, the approach provides a valuable research tool, the researchers said.
"It allows you to see exactly where enzymes are active within living animals," said Bogyo.
The Stanford researchers' ultimate goal is to test it in humans, though they'll complete more testing in animals before requesting permission from the U.S. Food and Drug Administration to conduct a human trial.
"Since there are currently no fluorescent imaging agents in use in humans, the approval process is likely to require significantly more pre-clinical data," Bogyo said.
In preparation, they are working with James Basilion, PhD, associate professor of biomedical engineering at Case Western Reserve University, who is using the probe in surgical procedures in animals. They are now testing the probe's ability to reveal the presence of glioma tumour cells during brain surgery in mice.
"Because glioma tumour tissue looks nearly identical to normal tissue, it's very difficult for surgeons to remove every last bit of it. We think this will help," said Bogyo.
The study is published in the Sept. 9 advance online issue of Nature Chemical Biology.