image: This Brian Callahan, assistant professor of biological chemistry at Binghamton University. view more
Credit: Jonathan Cohen
BINGHAMTON, NY - A Binghamton University biochemist has discovered a new way to fight cancer, one that attacks only the cancer cells and promises fewer side effects. He hunts hedgehogs.
Hedgehogs are proteins that help govern how cells develop. Normally, once a person reaches maturation, the hedgehogs turn off. But in some cancers -- prostate, pancreatic, ovarian and lung in particular -- the hedgehogs somehow turn back on, and force uncontrolled cell growth: cancer.
"Pharmaceutical companies have been after hedgehogs for years," says Brian Callahan, assistant professor of biological chemistry at Binghamton University. One in particular, Erivedge, binds with the same receptors that hedgehogs activate, blocking the cancer development. "We don't want to compete with Big Pharma," Callahan says. "We're trying a new strategy; we're going after hedgehogs directly."
Callahan recently published two papers, one about zinc and hedgehogs in the Journal of Biological Chemistry, and another about phenylarsine oxide in published by Chembiochem, in partnership with researchers from Rensselaer Polytechnic Institute.
Both substances don't simply block hedgehog reception; they shut hedgehogs down, preventing inactive hedgehogs from becoming biologically active and causing malignancies.
Callahan hasn't discovered the medicine, just the method.
"It's a proof of concept," he says of his work, which is funded by a $285,000, three-year Department of Defense "New Idea Development Award. "We can, with a small molecule, prevent the hedgehog from functioning. We think they bind a little differently. The arsenic seems to bind more tightly; it seems to be much more potent."
The next step is a partnership with Michelle Arkin, an associate professor at the University of California San Francisco's School of Pharmacy. During the next year or so, her lab will mirror Callahan's first experiments with 80,000 or so compounds in its library.
"We're looking for molecules that inhibit the functions that Brian found," Arkin says. She expects a hit rate of between 0.1 percent and 0.5 percent -- or maybe 100 or 200 compounds.
"There will be a lot of chemistry, a lot of tweaking," Arkin says. "What we'll get out of this is a puzzle piece," an idea of a molecule that disrupts the hedgehogs without causing undue side effects.
The best candidates will be tested in lab animals, probably sometime in 2017, Callahan says. After that? It's a matter of where the science leads.
"We want to get to molecularly targeted therapy," Callahan says. In essence, a magic bullet that kills the cancer and not the patient.
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Journal
Journal of Biological Chemistry