This is what it’s all about
- The goal is to identify cellular mechanisms underlying hereditary mitochondrial diseases and to establish therapies for people with these diseases.
- Using self-built disease models, researchers are testing the effect of promising molecules developed by pharmaceutical companies on disease progress.
- These efforts will increase understanding of mitochondrial diseases and related therapeutic opportunities.
When pharmaceutical companies on the other side of the world are looking for a research partner for their projects, they may look to Finland and Academy Professor Anu Wartiovaara. A research group head at the University of Helsinki, Wartiovaara is a global leader in the
“This really is extremely interesting work,” Wartiovaara sums up.
Mitochondrial diseases affect an estimated
Wartiovaara’s group investigates the mechanisms of mitochondrial diseases. Recently, they
“Our research has helped to provide diagnoses for thousands of patients around the world, and even treatments for some.”
So far, mitochondrial diseases cannot be cured, but new therapies are being investigated. Wartiovaara’s research has in fact provoked interest in international pharmaceutical companies, of which several have approached her over the years.
At the moment, Wartiovaara’s team is collaborating with two California-based pharmaceutical companies.
“Businesses make it possible to develop therapies in a way that would not be possible for an academic group on its own.”
Pharmaceutical companies are interested in disease models designed by Wartiovaara’s group, which have identified potential drug targets. In the collaborative projects, Wartiovaara and her colleagues are testing promising molecules developed by the companies to determine whether they affect disease progression. The results are published in scholarly articles, promoting research on mitochondrial diseases more broadly.
Wartiovaara and her group have also demonstrated that, at times, cellular metabolism can be redirected by relying on the body’s own regulators.
“You don’t always have to develop drug molecules for years on end.”
Tools for metabolic research have significantly advanced in the past three to five years.
Wartiovaara has also been involved in Finnish collaborative projects. In 2018, a working group she headed also received a
“Project results are published in a number of articles.”
Recently, Wartiovaara and her group received two grants from international foundations that give a significant boost to their research activities: €1.2 million from the
“We are very well known around the world.”
A couple of years ago, Wartiovaara and her colleagues established
“We already have customers on four continents.”
NADMED’s board includes Juha Tuominen, former CEO of HUS, and Ilkka Salonen, former CFO of the construction company YIT. Indeed, diving into the world of startups with the support of an expert group has been rewarding.
“For me, it’s been a tremendous learning experience,” Wartiovaara notes.
Please contact us and we will tailor a project to your needs: