Klaus Elenius
MD, PhD, professor
klaele@utu.fi +358 29 450 4393 +358 50 514 2307 Tykistökatu 6 A Turku ORCID identifier: https://orcid.org/0000-0001-5700-0827 |
ACTIONABLE RECEPTOR TYROSINE KINASE SIGNALING
Our goal is to understand how receptor tyrosine kinases (RTK) regulate the pathogenesis of human diseases, such as cancer. This information is needed for the development of molecularly targeted therapies. To recognize aberrations of RTK signaling in diseased tissue our laboratory also works on the molecular mechanism by which RTKs control normal processes, such as embryonic development. The work mainly focuses on the ErbB family of RTKs. Our laboratory has contributed to the field by e.g. by characterizing novel RTK signaling mechanisms, by identifying novel ErbB4 isoforms, and by determining the role of ErbBs and their ligands in angiogenesis.
Current topics
- Screens for predictive RTK mutations
- Novel RTK signaling mechanisms
- Development of preclinical models for development novel RTK inhibitors
- Sequencing of RTK inhibitor drug administration with cytotoxic agents
- In vitro “basket trials” with ErbB inhibitor drugs
- RTK signaling in angiogenesis and cardiovascular diseases
- RTKs in pediatric malignancies
- Biological role of novel ErbB4 isoforms in diseases and development
Elenius Lab members
- Anne Jokilammi, PhD
- Elli Narvi, PhD
- Deepankar Chakroborty, MSc
- Juho Heliste, MD
- Marika Koivu, MSc
- Johannes Merilahti, MSc
- Veera Ojala, MSc
- Janne Nordberg, MD
- Fred Saarinen, MSc
- Katri Vaparanta, MSc
- Kaisa Aalto, BM
- Maria Helkkula, BM
- Matias Mäenpää, BM
- Peppi Kirjalainen, BM
- Jori Torkkila, BM
- Database of recurrent mutations, an unbiased web resource to browse recurrent mutations in cancers (2026)
- iScience
(A1 Refereed original research article in a scientific journal) - Novel Genetic Risk Variants Associated with Oral Tongue Squamous Cell Carcinoma (2025)
- Head and Neck Pathology
(A1 Refereed original research article in a scientific journal) - Phosphoproteomic analysis reveals the diversity of signaling behind ErbB‐inhibitor‐induced phenotypes (2025)
- FEBS Journal
(A1 Refereed original research article in a scientific journal) - Recurrent cancer-associated ERBB4 mutations are transforming and confer resistance to targeted therapies (2025)
- Molecular Oncology
(A1 Refereed original research article in a scientific journal) - De Novo Multi-Omics Pathway Analysis Designed for Prior Data Independent Inference of Cell Signaling Pathways (2024)
- Molecular and Cellular Proteomics
(A1 Refereed original research article in a scientific journal) - DUSP6 inhibition overcomes neuregulin/HER3-driven therapy tolerance in HER2+ breast cancer (2024)
- Embo molecular medicine
(A1 Refereed original research article in a scientific journal) - Immunomodulatory Synthetic Glycocluster Molecule Prevents Melanoma Growth in vivo (2024)
- ChemBioChem
(A1 Refereed original research article in a scientific journal) - Trans-activating mutations of the pseudokinase ERBB3 (2024)
- Oncogene
(A1 Refereed original research article in a scientific journal) - STAT5b is a key effector of NRG-1/ERBB4-mediated myocardial growth (2023)
- EMBO Reports
(A1 Refereed original research article in a scientific journal) - An extracellular receptor tyrosine kinase motif orchestrating intracellular STAT activation (2022)
- Nature Communications
(A1 Refereed original research article in a scientific journal)



