Experimental drug could stop melanoma, other cancers, research suggests
Battling Melanoma
The critical protein blocked by pevonedistat is produced by the gene CDT2, and it is vital for malignant cancer cells to survive. Without it, the cells stop replicating and begin to fall apart. "We have great understanding now for how the drug works," Abbas said. "And we think the drug works not because of its intended target, but rather because it works on [the CDT2 protein] way downstream of that."
Excessive amounts of the protein are produced in melanoma cells, and patients with high levels of it are less likely to survive. "These tumors, and not necessarily just melanoma, they are addicted to this gene," Abbas said. "And that makes them very susceptible to the drug. In fact, we showed, that melanoma cells that have higher levels of expression of CDT2 are much more susceptible to the drug."
High levels of the CDT2 protein are also found in many other tumors, he noted, including brain, breast and liver tumors. Doctors may one day use the level of the protein as a way to gauge disease prognosis.
'We Have Great Hope'
The safety and effectiveness of pevonedistat in people is still being tested, and it is not yet available as a treatment. But Abbas, who has not been involved in the drug's testing, is optimistic based on his findings. "We have great hope that this drug will have very significant impact on melanoma in general. ... In fact, the drug is very effective on all melanomas, including those for which an effective therapeutic is lacking," he said. "We actually show this drug can work on melanoma that resisted treatment, which is a major challenge in melanoma therapy. ... If approved by the FDA and it moves forward, this drug could potentially be a good second-line therapy for those patients that fail initial treatment."
The findings have been published online by the scientific journal EBioMedicine. The research team consisted of Mouadh Benamar, Fadila Guessous, Kangping Du, Patrick Corbett, Joseph Obeid, Daniel Gioeli, Craig L. Slingluff Jr. and Abbas.
This work was supported by the National Cancer Institute, grant R00CA140774.
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