Magdalena Bodnar

Dr. Magdalena Bodnar


Research Focus & Metrics

Academic Career Length

18Years (2009-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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12 March 2014 in BioMed Research International
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PSPawel Sadlecki
Pawel Sadlecki
MBMagdalena Bodnar
Magdalena Bodnar
MGMarek Grabiec
Marek Grabiec
AMAndrzej Marszalek
Andrzej Marszalek
PWPawel Walentowicz
Pawel Walentowicz
MWMalgorzata Walentowicz-Sadlecka
Malgorzata Walentowicz-Sadlecka
Hypoxia-inducible factor-1α(HIF-1α), glucose transporter-1 (GLUT-1), and carbon anhydrase IX (CAIX) are important molecules that allow adaptation to hypoxic environments. The aim of our study was to investigate the correlation between HIF-1α, GLUT-1, and CAIX protein level with the clinicopathological features of endometrial cancer patients.Materials and Methods. 92 endometrial cancer patients, aged 37–84, were enrolled to our study. In all patients clinical stage, histologic grade, myometrial invasion, lymph node, and distant metastases were determined. Moreover, the survival time was assessed. Immunohistochemical analyses were performed on archive formalin fixed paraffin embedded tissue sections.Results. High significant differences(P=0.0115)were reported between HIF-1αexpression and the histologic subtype of cancer. Higher HIF-1αexpression was associated with the higher risk of recurrence(P=0.0434). The results of GLUT-1 and CAIX expression did not reveal any significant differences between the proteins expression in the primary tumor and the clinicopathological features.Conclusion. The important role of HIF-1αin the group of patients with the high risk of recurrence and the negative histologic subtype of the tumor suggest that the expression of this factor might be useful in the panel of accessory pathomorphological tests and could be helpful in establishing more accurate prognosis in endometrial cancer patients.

14 January 2016 in PLOS ONE
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JAJan Adamowicz
Jan Adamowicz
MPMarta Pokrywczyńska
Marta Pokrywczyńska
JTJakub Tworkiewicz
Jakub Tworkiewicz
SBShane V. van Breda
Shane V. van Breda
DTDominik Tyloch
Dominik Tyloch
TDTomasz Drewa
Tomasz Drewa
Due to the capacity of the amniotic membrane (Am) to support re-epithelisation and inhibit scar formation, Am has a potential to become a considerable asset for reconstructive urology i.e., reconstruction of ureters and urethrae. The application of Am in reconstructive urology is limited due to a poor mechanical characteristic. Am reinforcement with electrospun nanofibers offers a new strategy to improve Am mechanical resistance, without affecting its unique bioactivity profile. This study evaluated biocomposite material composed of Am and nanofibers as a graft for urinary bladder augmentation in a rat model. Sandwich-structured biocomposite material was constructed from frozen Am and covered on both sides with two-layered membranes prepared from electrospun poly-(L-lactide-co-E-caprolactone) (PLCL). Wistar rats underwent hemicystectomy and bladder augmentation with the biocomposite material. Immunohistohemical analysis (hematoxylin and eosin [H&E], anti-smoothelin and Masson’s trichrome staining [TRI]) revealed effective regeneration of the urothelial and smooth muscle layers. Anti-smoothelin staining confirmed the presence of contractile smooth muscle within a new bladder wall. Sandwich-structured biocomposite graft material was designed to regenerate the urinary bladder wall, fulfilling the requirements for normal bladder tension, contraction, elasticity and compliance. Mechanical evaluation of regenerated bladder wall conducted based on Young’s elastic modulus reflected changes in the histological remodeling of the augmented part of the bladder. The structure of the biocomposite material made it possible to deliver an intact Am to the area for regeneration. An unmodified Am surface supported regeneration of the urinary bladder wall and the PLCL membranes did not disturb the regeneration process. Am reinforcement with electrospun nanofibers offers a new strategy to improve Am mechanical resistance without affecting its unique bioactivity profile.

5 January 2017 in Journal of Cellular Biochemistry
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Anna BajekAnna Bajek
Anna Bajek
NGNatalia Gurtowska
Natalia Gurtowska
JOJoanna Olkowska
Joanna Olkowska
MMMalgorzata Maj
Malgorzata Maj
ŁKŁukasz Kaźmierski
Łukasz Kaźmierski
TDTomasz Drewa
Tomasz Drewa

1 January 2015 in Mediators of Inflammation
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AWAldona Wierzbicka-Rucińska
Aldona Wierzbicka-Rucińska
AHAnna Helmin-Basa
Anna Helmin-Basa
RGRenata Henryka Grzywa-Czuba
Renata Henryka Grzywa-Czuba
MCMieczyslawa Czerwionka-Szaflarska
Mieczyslawa Czerwionka-Szaflarska
ASAnna Szaflarska-Poplawska
Anna Szaflarska-Poplawska
KDKatarzyna Dzierzanowska-Fangrat
Katarzyna Dzierzanowska-Fangrat
Purpose. To investigate the expression of innate immunity components and cytokines in the gastric mucosa among H. pylori infected and uninfected children. Materials and Methods. Biopsies of the antral gastric mucosa from children with dyspeptic symptoms were evaluated. Gene expressions of innate immunity receptors and cytokines were measured by quantitative real‐time PCR. The protein expression of selected molecules was tested by immunohistochemistry. Results. H. pylori infection did not lead to a significant upregulation of MyD88, TLR2, TLR4, CD14, TREM1, and TREM2 mRNA expression but instead resulted in high mRNA expression of IL-6, IL-10, IFN-γ, TNF-α, and CD163. H. pylori cagA(+) infection was associated with higher IL-6 and IL-10 mRNA expression, as compared to cagA(−) strains. H. pylori infected children showed increased IFN‐γ and TNF‐α protein levels. IFN‐γ mRNA expression correlated with both H. pylori density of colonization and lymphocytic infiltration in the gastric mucosa, whereas TNF‐α protein expression correlated with bacterial density. Conclusion. H. pylori infection in children was characterized by (a) Th1 expression profile, (b) lack of mRNA overexpression of natural immunity receptors, and (c) strong anti‐inflammatory activities in the gastric mucosa, possibly resulting from increased activity of anti‐inflammatory M2 macrophages. This may explain the mildly inflammatory gastric inflammation often observed among H. pylori infected children.

27 August 2014 in PLOS ONE
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MPMarta Pokrywczyńska
Marta Pokrywczyńska
AJArkadiusz Jundzill
Arkadiusz Jundzill
JAJan Adamowicz
Jan Adamowicz
Tomasz KowalczykTomasz Kowalczyk
Tomasz Kowalczyk
KBKarolina Buchholz
Karolina Buchholz
TDTomasz Drewa
Tomasz Drewa
The purpose of this study was to compare: a new five-layered poly (L–lactide–co–caprolactone) (PLC) membrane and small intestinal submucosa (SIS) as a control in rat urinary bladder wall regeneration. The five-layered poly (L–lactide–co–caprolactone) membrane was prepared by an electrospinning process. Adipose tissue was harvested from five 8-week old male Wistar rats. Adipose derived stem cells (ADSCs) were seeded in a density of 3×106 cells/cm2 onto PLC membrane and SIS scaffolds, and cultured for 5-7 days in the stem cell culture medium. Twenty male Wistar rats were randomly divided into five equal groups. Augmentation cystoplasty was performed in a previously created dome defect. Groups: (I) PLC+ 3×106ADSCs; (II) SIS+ 3×106ADSCs; (III) PLC; (IV) SIS; (V) control. Cystography was performed after three months. The reconstructed urinary bladders were evaluated in H&E and Masson's trichrome staining. Regeneration of all components of the normal urinary bladder wall was observed in bladders augmented with cell-seeded SIS matrices. The urinary bladders augmented with SIS matrices without cells showed fibrosis and graft contraction. Bladder augmentation with the PLC membrane led to numerous undesirable events including: bladder wall perforation, fistula or diverticula formation, and incorporation of the reconstructed wall into the bladder lumen. The new five-layered poly (L–lactide–co–caprolactone) membrane possesses poorer potential for regenerating the urinary bladder wall compared with SIS scaffold.

20 December 2011 in Journal of Applied Genetics
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SHSylvia Hartmann
Sylvia Hartmann
MSMarcin Szaumkessel
Marcin Szaumkessel
ISItziar Salaverria
Itziar Salaverria
RSRonald Simon
Ronald Simon
GSGuido Sauter
Guido Sauter
MGMaciej Giefing
Maciej Giefing
Although down-regulation of GNG7 in cancer was reported before, its role in carcinogenesis is poorly understood. It belongs to a family of large G-proteins that may be involved in cell-contact-induced growth arrest and function in tumor suppression. In the present study, we stained immunohistochemically 188 tumors derived from larynx or floor of the mouth for GNG7 protein and confronted it with clinicopathologic data. Moreover, we performed bisulfite pyrosequencing to analyze GNG7 promoter methylation. We identified recurrent loss of GNG7 protein expression in 68/188 (36%) cases and promoter hypermethylation in (42/98; 43%) primary tumors, predominantly in young patients (p < 0.001). Loss of GNG7 expression correlated with hypermethylation of GNG7 promoter region (p < 0.001). Moreover, loss of GNG7 protein expression correlated with tumor size (p = 0.012) and lack of cervical metastasis (p = 0.02) whereas sustained expression correlated with keratinization (p = 0.008). Taken together, loss of GNG7 protein expression is a frequent event in head and neck cancer. Moreover, our data suggest that hypermethylation of the promoter region of GNG7 is probably the mechanism of the observed inactivation.