Kari Kurppa
PhD, Principal Investigator
kjkurp@utu.fi ORCID identifier: 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.
- Syövän täsmälääkehoitojen jälkeinen jäännöstauti (2020)
- Solubiologi
(D1 Article in a professional journal) - The guanine nucleotide exchange factor VAV3 participates in ERBB4-mediated cancer cell migration (2020)
- Journal of Biological Chemistry
(A1 Refereed original research article in a scientific journal) - Treatment-Induced Tumor Dormancy through YAP-Mediated Transcriptional Reprogramming of the Apoptotic Pathway (2020)
- Cancer Cell
(A1 Refereed original research article in a scientific journal) - A dominant-negative effect drives selection of TP53 missense mutations in myeloid malignancies (2019)
- Science
(A1 Refereed original research article in a scientific journal) - An unbiased in vitro screen for activating epidermal growth factor receptor mutations (2019)
- Journal of Biological Chemistry
(A1 Refereed original research article in a scientific journal) - The Mutational Profile of Unicystic Ameloblastoma (2019)
- Journal of Dental Research
(A1 Refereed original research article in a scientific journal) - Activating ERBB4 mutations in non-small cell lung cancer (2016)
- Oncogene
(A1 Refereed original research article in a scientific journal) - Early Dental Epithelial Transcription Factors Distinguish Ameloblastoma from Keratocystic Odontogenic Tumor (2015)
- Journal of Dental Research
(A1 Refereed original research article in a scientific journal) - Novel Targets for the Treatment of Ameloblastoma (2015)
- Journal of Dental Research
(A2 Refereed review article in a scientific journal ) - ERBB4 mutations in cancer and amyotrophic lateral sclerosis (2014) Kurppa Kari J.
(G5 Article dissertation ) - ERBB4 Promoter Polymorphism Is Associated with Poor Distant Disease-Free Survival in High-Risk Early Breast Cancer (2014)
- PLoS ONE
(A1 Refereed original research article in a scientific journal) - High frequency of BRAF V600E mutations in ameloblastoma (2014)
- Journal of Pathology
(A1 Refereed original research article in a scientific journal) - Overexpression of ERBB4 JM-a CYT-1 and CYT-2 isoforms in transgenic mice reveal isoform-specific roles in mammary gland development and carcinogenesis (2014)
- Breast Cancer Research
(A1 Refereed original research article in a scientific journal) - ERBB4 Mutations that Disrupt the Neuregulin-ErbB4 Pathway Cause Amyotrophic Lateral Sclerosis Type 19 (2013)
- American Journal of Human Genetics
(A1 Refereed original research article in a scientific journal) - Proteolytic Processing of ErbB4 in Breast Cancer (2012)
- PLoS ONE
(A1 Refereed original research article in a scientific journal) - Cell Death or Survival Promoted by Alternative Isoforms of ErbB4 (2010)
- Molecular Biology of the Cell
(A1 Refereed original research article in a scientific journal) - Somatic mutations of ErbB4: Selective loss-of-function phenotype affecting signal transduction pathways in cancer (2009)
- Journal of Biological Chemistry
(A1 Refereed original research article in a scientific journal)