A compound extracted from the Christmas berry primrose plant may stops the growth of uveal melanoma, according to preliminary tests.
With further testing, the discovery could lead to new therapeutic options for patients with uveal melanoma, report researches from the Sidney Kimmel Cancer Center (SKCC) -- Jefferson Health and the Icahn School of Medicine at Mt. Sinai
“I’m very optimistic,” says Jeffrey Benovic, PhD, Thomas Eakins Endowed Professor of Biochemistry & Molecular Biology at Thomas Jefferson University and an Associate Director with the SKCC, who led the new work. “If the results are confirmed in animal models and eventually humans, it could offer a new way to treat metastatic uveal melanoma patients down the road,” he adds.
The researchers tested whether a compound derived from an ornamental plant in the primrose family known as Ardisia crenata, might be able to fight the disease.
The compound, dubbed FR900359, or simply FR, was discovered 30 years ago from the plant’s leaves. FR works by blocking a particular type of G protein that sits on a cell’s membrane, called Gq – an important signaling molecule. But a subset of these proteins are mutated in uveal melanoma, turning on a molecular pathway that leads to cancer growth.
Dominic Lapadula, a graduate student in Dr. Benovic’s lab, grew three different types of uveal melanoma cells that have the cancer-spurring mutations in the lab. Then he treated the cells with FR.
“We didn’t expect it would work because previous research suggested a related compound called YM-254890 did not inhibit the mutated forms of the proteins found in uveal melanoma,” says Lapadula. “But lo and behold, FR very effectively blocked the growth of the uveal melanoma cells.” When the uveal melanoma cells were treated with small amounts of FR, the cells appeared to revert from cancer cells to typical melanocytes. “FR appears to be able to help reset the cells back to their normal state,” Dr. Benovic adds. “Ideally that’s what you want.”
Higher doses of FR killed the cells, the researchers report in the new study. The results suggest the compound could be an effective drug to treat uveal melanoma one day.
This study emanated from a team effort within the Cancer Cell Biology and Signaling program in the SKCC in collaboration with Dr. Julio Aguirre-Ghiso at the Icahn School of Medicine at Mt. Sinai. Next, Dr. Benovic would like to repeat the findings in a mouse model of uveal melanoma. To do so, he’ll team up with Takami Sato, MD, PhD, Director of the Metastatic Uveal Melanoma Program at Jefferson.
“I’m hopeful FR and related compounds will reset the cancer cells in the mouse model as it did in the cells we grew in the lab,” Dr. Benovic says, “getting it one step closer to testing in humans.”
“This outstanding work is part of a larger effort within our Center to develop new strategies for combating uveal melanoma. As one of the few cancer centers specializing in this aggressive cancer type, Dr. Benovic and team work closely with clinical partners within SKCC to fast track discoveries into the translational setting,” says Karen E. Knudsen, PhD, Enterprise Director of the Sidney Kimmel Cancer Center.
About Uveal Melanoma
Uveal melanoma forms in melanocytes. It accounts for about 5 percent of all melanoma cases. Surgery or radiation is the go-to treatment for patients with primary uveal melanoma that has not spread to other parts of the body. But metastases occur in about half of cases. The cancer most often travels to the liver. Once the cancer has spread, patients often only have a year or so to live as no effective therapies yet exist.
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