The gene that allows fireflies to flash is helping researchers track the effectiveness of anti-cancer drugs over time.
UT Southwestern Medical Center researchers are among the first to show that a technique called bioluminescence imaging (BLI) can be used to determine the effectiveness of cancer drugs that choke off a tumor's blood supply.
The technique requires a substrate called luciferin to be added to the bloodstream, which carries it to cells throughout the body. When luciferin reaches cells that have been altered to carry the firefly gene, those cells emit light.
Some cancer drugs, however, work by cutting off the blood supply to tumor cells. Given that luciferin is delivered via the vasculature, the researchers set out to determine the kinetics of luciferin delivery and whether BLI techniques could be used to gauge the effectiveness of drugs that destroy blood vessels that feed tumors.
They tested their theory in mice bearing human breast-cancer tumors. Before being introduced to the animals, the tumor cells had been transfected with the firefly gene, which becomes part of the cells as they divide and grow just like genetically modified, herbicide-resistant food crops.
For the study, researchers used BLI to monitor light emissions from tumors following administration of the luciferin. While the mice didn't visibly glow, the researchers used special light-detecting equipment to observe strong correlations between the amount of light emitted and the size of the tumor as it grew. Detected light emission, however, was severely reduced after the vascular-disrupting drug was administered.
"What we've done is offer proof-of-concept that BLI may be an effective and cheaper method to assess drug development and effectiveness," said Dr. Ralph Mason, professor of radiology, director of the UT Southwestern Cancer Imaging Center and senior author of the study. "The technique is not intended to be used for imaging tumors or diagnosing cancer in humans, but it potentially allows us to do much more efficient pre-clinical experiments."
Dr. Mason stressed that light-emission kinetics depend heavily on tumor location.
The findings are available online and in a future issue of the Journal of the Federation of American Societies for Experimental Biology.
Although magnetic resonance imaging (MRI) remains the gold standard of medical imaging, BLI has its advantages. The noninvasive procedure allows detection of cell viability not accessible by MRI and is less costly, according to researchers at UT Southwestern.
"Ultimately, the MRI is much more sophisticated and can do more, but BLI is very straight-forward," Dr. Mason said. "It's perfect for evaluating new classes of drugs designed to cause acute vascular changes in tumors because the tests are inexpensive and easy to do."
Dr. Mason said it's critically important to develop new chemotherapeutic drugs because existing therapies, when used on their own, are far from ideal. "We're lacking the optimal drugs as demonstrated by the people who are not cured by chemotherapy," he said.
He said many existing drugs kill 99 percent of a tumor but allow a few cells to survive, giving the tumor an opportunity to grow back.
"Therefore, you need to do a lot of tests to optimize dosing, optimize repeat delivery and probably optimize the co-administration of other, more traditional drugs or therapies," he said. "BLI provides an opportunity to do those tests cheaply and efficiently."