Author
Listed:
- Frederik Rastfeld
(Research Centre Juelich)
- Marco Hoffmann
(Research Centre Juelich)
- Sylvie Krüger
(Research Centre Juelich)
- Patrick Bohn
(Helmholtz Centre for Infection Research)
- Anne-Sophie Gribling-Burrer
(Helmholtz Centre for Infection Research
UPR9002)
- Laura Wagner
(Research Centre Juelich)
- Nils Hersch
(Research Centre Juelich)
- Carina Stegmayr
(Research Centre Juelich)
- Lukas Lövenich
(Research Centre Juelich)
- Sven Gerlach
(Research Centre Juelich)
- Daniel Köninger
(Research Centre Juelich)
- Christina Hoffmann
(Research Centre Juelich)
- Helene L. Walter
(Research Centre Juelich
Department of Neurology)
- Dirk Wiedermann
(Multimodal Imaging Group)
- Hajaani Manoharan
(Research Centre Juelich)
- Gereon R. Fink
(Research Centre Juelich
Department of Neurology)
- Rudolf Merkel
(Research Centre Juelich)
- Heribert Bohlen
(SRTD biotech GmbH)
- Redmond P. Smyth
(Helmholtz Centre for Infection Research
UPR9002)
- Maria A. Rueger
(Research Centre Juelich
Department of Neurology)
- Bernd Hoffmann
(Research Centre Juelich)
Abstract
Targeting of diseased cells is one of the most urgently needed prerequisites for a next generation of potent pharmaceuticals. Different approaches pursued fail mainly due to a lack of specific surface markers. Developing an RNA-based methodology, we can now ensure precise cell targeting combined with selective expression of effector proteins for therapy, diagnostics or cell steering. The specific combination of the molecular properties of antisense technology and mRNA therapy with functional RNA secondary structures allowed us to develop selectively expressed RNA molecules for medical applications. These seRNAs remain inactive in non-target cells and induce translation by partial degradation only in preselected cell types of interest. Cell specificity and type of functionalization are easily adaptable based on a modular system. In proof-of-concept studies we use seRNAs as platform technology for highly selective cell targeting. We effectively treat breast tumor cell clusters in mixed cell systems and shrink early U87 glioblastoma cell clusters in the brain of male mice without detectable side effects. Our data open up potential avenues for various therapeutic applications.
Suggested Citation
Frederik Rastfeld & Marco Hoffmann & Sylvie Krüger & Patrick Bohn & Anne-Sophie Gribling-Burrer & Laura Wagner & Nils Hersch & Carina Stegmayr & Lukas Lövenich & Sven Gerlach & Daniel Köninger & Chris, 2025.
"Selectively expressed RNA molecules as a versatile tool for functionalized cell targeting,"
Nature Communications, Nature, vol. 16(1), pages 1-17, December.
Handle:
RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-024-55547-6
DOI: 10.1038/s41467-024-55547-6
Download full text from publisher
Corrections
All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-024-55547-6. See general information about how to correct material in RePEc.
If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.
We have no bibliographic references for this item. You can help adding them by using this form .
If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.
For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .
Please note that corrections may take a couple of weeks to filter through
the various RePEc services.