Scientists develop first drug-like compounds to inhibit elusive cancer-linked enzymes

lab
Credit: CC0 Public Domain

A team of scientists from the University of Michigan Rogel Cancer Center has developed the first drug-like compounds to inhibit a key family of enzymes whose malfunction is associated with several types of cancer, including an aggressive form of childhood leukemia.

The enzymes—known as the -binding SET domain (NSD) family of histone methyltransferases—have long been an attractive drug target, but efforts to attack them have previously proved elusive because the shape of the binding sites in these enzymes makes it difficult for drug-like molecules to bind to it.

The research team—led by Tomasz Cierpicki, Ph.D., and Jolanta Grembecka, Ph.D.—used a variety of techniques including X-ray crystallography and to develop first-in-class inhibitors of a key protein known as NSD1, according to findings published in Nature Chemical Biology.

The team's lead compound—known as BT5—showed promising activity in leukemia cells with the NUP98-NSD1 that is seen in a subset of pediatric leukemia patients.

"Our study, which was years in the making, demonstrates that targeting this key enzyme with small-molecule inhibitors is a feasible approach," says Cierpicki, an associate professor of biophysics and pathology at U-M. "These findings will facilitate the development of the next generation of potent and selective inhibitors of these enzymes, which are overexpressed, mutated or undergo translocations in several types of cancer."


Explore further

Researchers develop new potential drug for rare leukemia

More information: Huang Huang et al, Covalent inhibition of NSD1 histone methyltransferase, Nature Chemical Biology (2020). DOI: 10.1038/s41589-020-0626-6
Journal information: Nature Chemical Biology

Citation: Scientists develop first drug-like compounds to inhibit elusive cancer-linked enzymes (2020, August 31) retrieved 5 August 2021 from https://phys.org/news/2020-08-scientists-drug-like-compounds-inhibit-elusive.html
This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no part may be reproduced without the written permission. The content is provided for information purposes only.
87 shares

Feedback to editors

User comments