DNA binding is essential for effectiveness of steroids
Finding cortisone alternatives with fewer side effects
A group of scientists around Henriette Uhlenhaut, Professor for Metabolic Programming at TUM School of Life Sciences in Freising-Weihenstephan and researcher in the field of Molecular Endocrinology at Helmholtz Zentrum München is working with so-called glucocorticoids. These are steroidal hormones such as cortisone, which are released by the adrenal glands every day before waking up or whenever a person is subjected to stress. These steroids are bound to their glucocorticoid receptor and control not only our body’s immune reaction but also our sugar and fat metabolism.
As glucocorticoid receptors are so efficient at disabling immune reactions, synthetic steroid medication is among the most prescribed drugs overall and it has been for decades.
The goal: Finding molecules with anti-inflammatory effects
“Unfortunately, this useful property leads to severe side effects as one hormone or drug causes different effects in other non-immune cells,” explained the professor. Among these effects are the reduction of muscle mass or the deposition of fat.
“We still don’t fully understand the effects of steroid compounds,” said Uhlenhaut. With her team, she wants to discover the molecular mechanisms that steroids such as cortisone utilize to stop inflammatory reactions.
As soon as researchers know how cortisone works, so how it mutes inflammation genes in immune system cells, they can begin looking for molecules that possess the same anti-inflammatory properties as cortisone, but with fewer side effects.
Common theory refuted
Until recently, scientists believed that the steroids‘ anti-inflammatory effect was based on protein-to-protein interaction. It was assumed that the glucocorticoid receptor – in other words, the protein that binds these drugs or hormones – would connect to other inflammation inducing proteins without any DNA contact.
Using a new preclinical model, the team of researchers could now demonstrate that DNA binding is required for these drugs to have an effect; for years, scientists had assumed that this was not the case. Without the glucocorticoid receptor (the protein that binds these drugs or hormones) enabling DNA binding to chromosomes, chromatin or genes, there is no biological effect.
A milestone for drug development
“Now we know that DNA binding plays a major role, yet we have not found a way to separate side effects from the desired effects,” explained Prof. Uhlenhaut. Regarding COVID-19, researchers do not have a clear answer either as to why these kinds of treatments are successful. Further research in this area is required.
Until now, various approaches focused on protein-to-protein contact, which might explain why these have not been successful. As this basic approach can now be discarded, further research regarding drug development of cortisone alternatives can now focus on the DNA.
Laura Escoter-Torres, Franziska Greulich, Fabiana Quagliarini, Michael Wierer, Nina Henriette Uhlenhaut (2020): Anti-inflammatory functions of the glucocorticoid receptor require DNA binding
Nucleic Acids Research, DOI:10.1093/nar/gkaa565
This research paper was created by researchers at TUM in cooperation with colleagues from Helmholtz Zentrum München and the Max Planck Institute of Biochemistry (MPIB) in Martinsried near Munich.
Henriette Uhlenhaut, Professor for Metabolic Programming, is a member of ZIEL – Institute for Food & Health, an interdisciplinary corporate research center at TUM.
Technical University of Munich
Corporate Communications Center
- Dr. Katharina Baumeister
- katharina.baumeister@tum.de
- presse@tum.de
- Teamwebsite
Contacts to this article:
Prof. Dr. Henriette Uhlenhaut
Chair for Metabolic Programming
Technical University of Munich
TUM School of Life Sciences
ZIEL – Institute for Food & Health
Tel.: +49 (0) 8161 71 4322
henriette.uhlenhaut@tum.de