Kari Kurppa
PhD, Principal Investigator
kjkurp@utu.fi ORCID-tunniste: https://orcid.org/0000-0001-8286-2429 |
Principal Investigator 2020 -> ; Institute of Biomedicine, University of Turku
Senior Researcher (erikoistutkija) 2019-2020 ; Institute of Biomedicine, University of Turku
Post-doctoral Fellow 2016-2019 ; Dana-Farber Cancer Institute, Harvard Medical School, Boston, USA. Mentor: Professor Pasi A. Jänne
PhD 2014 ; Medical Biochemistry and Genetics, University of Turku
MSc (Biochemistry) 2008 ; University of Turku
The Cancer Drug Resistance laboratory aims to understand the means cancer cells use to develop resistance to cancer therapies. Our special focus are the mechanisms that enable the establishment of minimal residual disease, or govern the maintenance of residual tumors following targeted cancer therapy. The overarching goal of our research is to develop rational combination strategies that will extend the long-term efficacy of clinically used cancer therapies.
While targeted therapy has transformed the treatment of cancer, the long-term efficacy of these strategies is hampered by acquired drug resistance. In many cases, clinical drug resistance is preceded by minimal residual disease (MRD) state, where residual tumors stay dormant for an extended period of time. Emerging evidence indicates that the establishment of MRD is mainly regulated by non-genetic mechanisms, as cancer cells adapt to treatment by acquiring new phenotypic states that no longer depend on the targeted oncogene. These slow-cycling drug tolerant cells can regain proliferative state upon drug withdrawal or acquisition of additional resistance mechanisms, and as such serve as a reservoir of dormant cells capable of re-initiating the growth of a drug resistant tumor. Understanding the mechanisms underlying the establishment or maintenance of minimal residual disease would enable the development of rational combination strategies aimed to prevent or limit residual disease, leading to prolonged survival of cancer patients.
- Bone marrow failure, somatic rescue by p53 inactivation, and enhanced leukemogenesis in germ line ERCC6L2 disease (2026)
- Blood
(A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä ) - Database of recurrent mutations, an unbiased web resource to browse recurrent mutations in cancers (2026)
- iScience
(A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä ) - Complement components C1r and C1s promote oral squamous cell carcinoma cell proliferation (2025)
- Journal of oral biosciences
(A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä ) - LIMA1-alpha staining predicts curative intent surgery response in HPV negative head and neck cancer (2025)
- Embo molecular medicine
(A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä ) - Recurrent cancer-associated ERBB4 mutations are transforming and confer resistance to targeted therapies (2025)
- Molecular Oncology
(A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä ) - The pathogenesis of therapy-related myeloid neoplasms from TP53-mutant clonal hematopoiesis (2025)
- Leukemia
(A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä ) - The Prolonged Half-Life of the p53 Missense Variant R248Q Promotes Accumulation and Heterotetramer Formation with Wildtype p53 to Exert the Dominant-Negative Effect (2025)
- Cancer Research
(A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä ) - DUSP6 inhibition overcomes neuregulin/HER3-driven therapy tolerance in HER2+ breast cancer (2024)
- Embo molecular medicine
(A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä ) - Immunomodulatory Synthetic Glycocluster Molecule Prevents Melanoma Growth in vivo (2024)
- ChemBioChem
(A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä ) - Targeting the mevalonate or Wnt pathways to overcome CAR T-cell resistance in TP53-mutant AML cells (2024)
- Embo molecular medicine
(A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä )



