A team of researchers from USC and NYU has developed and patented a small molecule that interferes with cancer progression with minimal side effects.
The molecule prevents two critical proteins from interacting by mimicking the surface topography of one protein—like wearing a mask— which tricks the other protein into binding with it. This stops a transcription factor that can create aberrant gene expression and contribute to cancer growth.
Because of the molecule’s precision in targeting the protein interaction, it does not appear to produce any side effects when tested on animal tumor models.
Precision to target cancer growth
“This complex represents one of the key focal points in tumor-promotion,” said Bogdan Olenyuk, assistant professor of pharmacology and pharmaceutical sciences at the USC School of Pharmacy and one of two corresponding authors on a paper about the work. “However, targeting it for therapeutic intervention was a major challenge, since transcription factors do not possess the necessary topographical structures to make them good targets for mimicking drugs.”
Instead, the team focused on blocking one of the transcription factor’s binding partners—a large protein with complex topography that makes it an easier, more “druggable” target.
Teams of researchers from USC and NYU collaborated on the study. Olenyuk led the USC group, which included graduate students Ivan Grishagin and researcher Hanah Mesallati. Paramjit Arora, professor of chemistry at NYU and co-corresponding author on the paper, lead the NYU group, which included graduate student Brooke Bullock Lao and Thomas Brewer.
Their study appears this week in the Proceedings of the National Academy of Sciences. The researchers have filed patent applications for the new design, which has already attracted the interest of several pharmaceutical companies.
Transcription factors as targets
Targeting protein-protein interactions has been a longstanding goal of researchers in the field of cancer biology. It’s been the focus of Olenyuk’s research since 2008.
“After completing my postdoctoral project in cancer gene regulation with my mentor Peter Dervan at Caltech and our collaborator Bill Kaelin at Harvard Medical School, I decided to make a major focus of my research on an interdisciplinary problem of targeting oncogenic transcription factors with designed drug-like molecules,” he said.
The researchers used Rosetta Software, a design software for molecular structures, to guide their design. They then designed a strategy to graft the specially textured surface onto a stable scaffold.
So far, the molecules have only been tested in the lab, but the researchers intend to translate the compounds into clinical studies.