
Phd hab Dorota Nowak
professor
Department of Cell Pathology
Head
Department of Cell Pathology
Chair of the scientific discipline board
Faculty of Biotechnology
dorota.nowak@uwr.edu.pl
tel. +48 71 375 62 89
Interested
- biochemistry molecular biology
- melanoma
- general science technology
- adipocytes
- tumor microenvironment
- cancer associated adipocytes
- cancer‑associated adipocytes
- cancer associated adipocytes caas
- targeted therapy
- tumor microenvironment tme
Scientific discipline
- medical sciences
- biotechnology
Latest publications
- Mutual impact of adipocytes and colorectal cancer cells growing in co-culture conditions
- Changes in biomechanical properties of A375 cells due to the silencing of TMSB4X expression are not directly correlated with alterations in their stemness features.
- Gelsolin contributes to the motility of A375 melanoma cells and this activity is mediated by the fibrous extracellular matrix protein profile.
- PARP1 as a marker of an aggressive clinical phenotype in cutaneous melanoma - a clinical and an in vitro study.
- Evaluation of apelin and apelin receptor level in the primary tumor and serum of colorectal cancer patients.
- The impact of cellular elements of TME on melanoma biology and its sensitivity to EGFR and MET targeted therapy
- Characterization of Melanoma Cell Lines Resistant to Vemurafenib and Evaluation of Their Responsiveness to EGFR- and MET-Inhibitor Treatment
- Melanoma Progression under Obesity: Focus on Adipokines
- Melanoma stimulates the proteolytic activity of HaCaT keratinocytes
- The Influence of Tumor Microenvironment on Immune Escape of Melanoma
- Hypoxia and Extracellular Acidification as Drivers of Melanoma Progression and Drug Resistance
- Melanoma cells with diverse invasive potential differentially induce the activation of normal human fibroblasts
- Stromal Cells Present in the Melanoma Niche Affect Tumor Invasiveness and Its Resistance to Therapy
- Melanoma cells induce dedifferentiation and metabolic changes in adipocytes present in the tumor niche
- Combination of selected MET and EGFR inhibitors decreases melanoma cells’ invasive abilities.
- Expression level of EGFR and MET receptors regulates invasiveness of melanoma cells.
- Thymosin β4 regulates focal adhesion formation in human melanoma cells and affects their migration and invasion.
- The two faces of platinum hydrospirophosphorane complexes. Not only relevant catalysts but cytotoxic compounds as well.
- Combinations of EGFR and MET inhibitors reduce proliferation and invasiveness of mucosal melanoma cells
- Alpha-Enolase (ENO1) correlates with invasiveness of cutaneous melanoma - an in vitro and a clinical study.