A molecule that would inhibit the action of yeast genes was being searched by Cha, a graduate student in cell and molecular biology at the university. She found that thiabendazole did the trick.
She then tested the drug in developing frog embryos. These are fast growing vertebrates in which scientists can watch blood vessel growth in living animals.
Cha found that frog embryos grown in water with the drug either didn't grow blood vessels or grew blood vessels that were then dissolved away by the drug. Interestingly, when the drug was removed, the embryos' blood vessels grew back.
"We didn't set out to find a vascular disrupting agent, but that's where we ended up," said Wallingford, associate professor of developmental biology and Cha's graduate advisor with Marcotte. "This is an exciting example of the power of curiosity-driven research and the insights that can come from blending disciplines in biology."
The scientists' goal is now to move the drug into clinical trials with humans. They are talking with clinical oncologists about next steps.
"We hope the clinical trials will be easier because it is already approved by the FDA for human use," said Marcotte.