Irina Elcheva, PhD - Penn State Cancer Institute
Researcher Profile
Irina Elcheva, PhD
Division of Hematology and Oncology
Penn State Neuroscience Institute
Research Interests
Dr. Irina Elcheva's research focuses on understanding the regulation of gene expression in human development and cancer. Current projects in Dr. Elcheva's laboratory investigate regulatory pathways of self-renewal and differentiation in normal and malignant stem/progenitors cells with a focus on the hematopoietic system, including regulation of gene expression in leukemia-initiating cells and modeling of myeloid blood development by transcriptional programming of human induced pluripotent stem cells (hiPSCs).
Dr. Elcheva received her training in stem cell biology in the laboratory of Dr. Igor Slukvin at UW-Madison, Wisconsin, where she discovered that co-expression of endothelial and hematopoietic transcription factors e.g., ETV2 and GATA2, induces hiPSCs' differentiation to blood cells with pan-myeloid phenotype. Currently, Dr. Elcheva investigates the application of the direct programming of hiPSC-based systems for disease modeling and drug toxicity screening.
Besides transcriptional programming, Dr. Elcheva's lab investigates RNA-binding proteins (RBPs) that play an important role in maintaining potency and proliferation. Dr. Elcheva, the lead author of the study, showed that Insulin-like growth factor 2 mRNA-binding proteins (IGF2BPs) maintain leukemia stem cell properties by regulating transcriptional and metabolic regulators of stemness: HOXB4, MYB, and ALDH1A1. In a recent collaborative study, Dr. Elcheva's, Dr. Schell's, and Dr. Spiegelman's research teams demonstrated that IGF2BPs suppress innate and adaptive immune responses in cancer cells and tumor microenvironment. Currently, Dr. Elcheva's lab investigates the dual role of IGF2BPs in supporting proliferation and inhibiting immune responses, and mechanisms of IGF2BP-mediated immunogenicity in liquid and solid tumors. The ultimate goal of Dr. Elcheva's research is to develop new and improve existing treatments of refractory and relapsed pediatric cancers by targeting cellular processes of self-renewal and differentiation.
- Messenger RNA
- Neoplasms
- Genes
- Pluripotent Stem Cells
- RNA-Binding Proteins
- Leukemia
- Stem Cells
- Hemangioblasts
- Insulin-Like Growth Factor Binding Protein 2
- Transcription Factors
- Ligases
- Ubiquitin