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Dive into the research topics where Famulski W is active.

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Featured researches published by Famulski W.


Tumori | 2006

Levels of VE-cadherin increase independently of VEGF in preoperative sera of patients with colorectal cancer.

Mariola Sulkowska; Famulski W; Wincewicz A; Moniuszko T; Kedra B; Koda M; Zalewski B; Baltaziak M; Stanislaw Sulkowski

Aims and Background Vascular endothelial cadherin (VE-cad-herin) preserves the tightness of the mature vascular network as a component of endothelial adherens junctions. Vascular endothelial growth factor (VEGF) makes VE-cadherin dissociate from complexes with β-catenin, so that endothelial cells can loosely proliferate and migrate. We searched for relationships between VEGF and VE-cadherin levels in preoperative sera of patients with colorectal cancer (CRC). We also compared VE-cadherin levels of control and preoperative CRC sera in relation to clinicopathological features. Methods We measured with an ELISA kit the serum levels of the proteins in preoperative samples from 125 CRC patients and in samples from 16 healthy volunteers. Results Serum VE-cadherin was about fourfold higher in CRC patients than in controls (P <0.00001), with similar results being found in subgroups with different clinicopathological features versus controls. VE-cadherin was not correlated with VEGF in the entire group of CRC patients nor in the subgroups of node-positive and node-negative patients, different grades of histological differentiation (G2 or G3), extent of tumor growth (pT1+pT2 or pT3+pT4), histopathological type (adenocarcinoma or mucinous carcinoma), sex, age, and tumor site (colon or rectum). However, the serum levels of VE-cadherin and VEGF in CRC patients, which were higher than the mean values of controls, tended towards a negative correlation in node-positive patients (P = 0.078, r = -0.279). Conclusions VEGF and VE-cadherin seem to be independent markers of angiogenesis in CRC with no significant correlation between their serum levels.


Oncology Letters | 2014

E-cadherin and β-catenin adhesion proteins correlate positively with connexins in colorectal cancer.

Luiza Kanczuga-Koda; Andrzej Wincewicz; Andrzej Fudala; Tomasz Abrycki; Famulski W; Marek Baltaziak; Stanislaw Sulkowski; Mariusz Koda

The majority of solid cancers present with qualitative and quantitative aberrations of adhesion proteins, including E-cadherin and β-catenin, and connexin (Cx) gap junction proteins, which is consistent with alterations in the expression and location of such proteins in neoplastic cells. Since there are no data on the correlation between adhesion proteins and Cxs in human colorectal cancer (CRC), the aim of the present study was to evaluate the expression and correlation between these proteins. Tissue specimens were obtained from 151 cases of surgically removed colorectal adenocarcinomas. The samples were examined by immunohistochemistry with the use of antibodies against E-cadherin, β-catenin and the three Cxs: Cx26, Cx32 and Cx43. The aberrant expression of the studied adhesion proteins (primarily cytoplasmic for E-cadherin and cytoplasmic and/or nuclear for β-catenin) was observed, whereas only a minority of cases revealed normal membranous distribution of the labeling. The present study is the first in the literature to reveal a correlation between the expression of E-cadherin and β-catenin and the examined Cxs in CRC in humans. The positive correlation between the Cxs, particularly Cx26 and Cx32, and the adhesive proteins occurred in patients without lymph node metastases and in the moderately differentiated tumors (G2). Such a dependency was not observed in the analysis of the correlation between Cx43 and E-cadherin. However, a positive correlation between these proteins was observed in patients with lymph nodes metastases. Additionally, a link between the expression of these adhesion proteins was observed. The present study indicates, for the first time, that the expression of adhesion proteins, E-cadherin and β-catenin, is closely associated with the expression of three studied Cxs in CRC, and that this correlation may improve an understanding of the carcinogenic process in this cancer.


Tumori | 2001

Bcl-2 expression in primary uveal melanoma.

Mariola Sulkowska; Famulski W; Alina Bakunowicz-Lazarczyk; Lech Chyczewski; Stanislaw Sulkowski

Aims Uveal malignant melanoma is the most common intraocular tumor. The aim of this study was the analysis of bcl-2 oncoprotein expression in this tumor type. The melanomas were evaluated according to tumor location and patient age and sex. The relationship between bcl-2 expression and histological type, clinicopathologic stage and the presence of a set of predetermined morphological parameters was analyzed. Methods The study involved 39 patients with ocular melanomas treated with surgery alone between 1983 and 1997. Formalin-fixed, paraffin-embedded tissues were treated with anti-bcl-2 antibody (Dako No M0887). Immunolocalization of the bcl-2 oncoprotein was performed using the labeled streptavidin biotin (LSAB) method. bcl-2 expression in neoplastic cells was evaluated in a semiquantitative manner: lack of reactivity was defined as bcl-2 negative, reactivity present in less than 30% of cells as low bcl-2, and reactivity in more than 30% of cells as high bcl-2. The percentage of cells with a positive reaction was assessed independently by two pathologists, and the results were subjected to statistical analysis using Fischers exact test. Results and conclusion No statistically significant correlation was found between the expression of bcl-2 oncoprotein and the clinicopathologic features analyzed. However, the high percentage of tumors with positive expression of this oncoprotein suggests that it plays a significant role in the biology of uveal melanoma.


Clinical Chemistry and Laboratory Medicine | 2009

Hypoxia related growth factors and p53 in preoperative sera from patients with colorectal cancer - evaluation of the prognostic significance of these agents

Stanislaw Sulkowski; Andrzej Wincewicz; Bogdan Zalewski; Famulski W; Joanna Maria Lotowska; Mariusz Koda; Maria Elzbieta Sobaniec-Lotowska; Michal Mysliwiec; Marek Baltaziak; Krystyna Pawlak; Mariola Sulkowska

Abstract Background: Insulin-like growth factor-I (IGF-I) and vascular endothelial growth factor (VEGF) belong to a group of hypoxia related proteins. IGF-I induces expression of VEGF and decomposes wild type p53 in cancer cell lines. The goal of our study was to evaluate serum IGF-I, VEGF and p53 with respect to overall and disease free survival of patients with colorectal cancer (CRC) patients compared with healthy volunteers. Methods: Preoperative blood samples from 125 patients with CRC and 16 healthy volunteers were examined using ELISA for serum IGF-I, p53 and VEGF concentrations. Results: Concentrations of p53 and VEGF were significantly higher in CRC patients than in controls (p<0.0006 and p<0.0001, respectively). IGF-I was not statistically different between both groups. Serum IGF-I showed negative correlation with p53 in CRC patients (p<0.04, r=−0.193). IGF-I and VEGF showed negative correlation in poorly differentiated cancers (G3) (p<0.03, r=−0.339). Patients with VEGF concentrations that were above average for the cancer population survived for a shorter period of time (p=0.065 in evaluation of overall survival and 0.071 in estimation of disease-free survival during a 3-year follow-up) compared with patients with serum VEGF lower than the highest values seen in controls. Conclusions: Comparisons between serum IGF-I and p53 appear to confirm the metabolism of p53 by IGF-I. Serum VEGF showed prognostic significance in our study. Serum concentrations of IGF-I and VEGF did not show positive correlation, as expected due to IGF-I induction of VEGF in malignant colon cell lines. Clin Chem Lab Med 2009;47:1439–45.


Oncology Letters | 2017

Stromal and intraepithelial tumor‑infiltrating lymphocytes in colorectal carcinoma

Katarzyna Jakubowska; Kisielewski W; Luiza Kańczuga‑Koda; Mariusz Koda; Famulski W

The local mechanisms of antitumor immune defense determine the development and organization of the tumor microenvironment, and the composition and relative proportions of the inflammatory cell population affect the quality and characteristics of the immune response. The aim of the present study was to conduct a quantitative morphological evaluation of two types of tumor-infiltrating lymphocyte (TILs) populations, including those located in the stroma and intraepithelial cancer structures, in the invasive front and the center of the tumor in patients with colorectal cancer (CRC). The study included 160 patients with CRC who had undergone surgery. The tissue material was stained with hematoxylin and eosin, as used in routine histopathological diagnosis, and the two TIL populations were observed and counted with light microscopy. The relative extent of infiltration of stromal and intraepithelial TILs into the front and center of the primary tumors was similar. The extent of infiltration by stromal TILs was negatively correlated with the morphological features of tumor progression including the cancer infiltration of blood vessels (P=0.016), the invasion of lymph vessels (P=0.007), perineural invasion (P=0.036), lymph node involvement (P=0.047) and distant metastases (P=0.032). The infiltration by intraepithelial TILs was positively correlated with a desmoplastic reaction (P=0.002). Disease-free survival time was statistically shorter in patients without intraepithelial TILs in the center of the primary tumor mass (P=0.049; hazard ratio = 1.45). These results confirm that the infiltration of TILs into the invasive front and center of the tumor in patients with CRC serves an important role in the invasion and progression of the disease, and should be considered in routine histopathological examinations.


Molecular and Clinical Oncology | 2018

Squamous cell carcinoma of the breast as a clinical diagnostic challenge

Katarzyna Jakubowska; Luiza Kańczuga‑Koda; Kisielewski W; Mariusz Koda; Famulski W

Squamous cell carcinoma (SqCC) of the breast should be differentiated between the primary skin keratinizing squamous carcinoma and squamous metaplastic cancer. In the current study, the cases of two patients who were diagnosed with SqCC originated from skin and the breast were discussed. A fine-needle aspiration biopsy confirmed the presence of atypical squamous cells. In both cases, the microscopic examination of the surgical specimen revealed a malignant neoplasm differentiated into SqCC characterized by keratinizing cancer cells with abundant eosiphilic cytoplasm with large, hyperchromatic vesicular nuclei. Immunohistochemical studies showed negative for progesterone and estrogen receptors and human epidermal growth factor receptor 2. Moreover, negative expression of cytokeratin 7 and 20 was confirmed. The diagnosis of the both tumors was established based on the detailed analysis of clinical, macroscopical and microscopical information. SqCC localized in the breast is a great diagnostic challenge in pathomorphology and more attention should be paid for analysis of such lesions in daily practice.


European Journal of Internal Medicine | 2007

STAT1 and STAT3 as intracellular regulators of vascular remodeling.

Andrzej Wincewicz; Mariola Sulkowska; Ryszard Rutkowski; Stanislaw Sulkowski; Musiatowicz B; Tomasz Hirnle; Famulski W; Mariusz Koda; Grzegorz Sokol; Przemyslaw Szarejko


Folia Morphologica | 2003

Expression of connexin 43 in breast cancer in comparison with mammary dysplasia and the normal mammary gland

Luiza Kanczuga-Koda; Mariola Sulkowska; Mariusz Koda; Joanna Reszec; Famulski W; Marek Baltaziak; Stanislaw Sulkowski


Folia Histochemica Et Cytobiologica | 2013

Immunohistochemical expression of MMP-7 protein and its serum level in colorectal cancer

Anna Pryczynicz; Mariusz Gryko; Katarzyna Niewiarowska; Violetta Dymicka-Piekarska; Marek Ustymowicz; Maciej Hawryluk; Dariusz Cepowicz; Agnieszka Borsuk; Andrzej Kemona; Famulski W; Katarzyna Guzińska-Ustymowicz


Folia Histochemica Et Cytobiologica | 2001

CD44 expression in colorectal cancer. An immunohistochemical study including correlation with cathepsin D immunoreactivity and some tumour clinicopathological features.

Zalewski B; Famulski W; Mariola Sulkowska; Maria Elzbieta Sobaniec-Lotowska; Z Piotrowski; Kisielewski W; Stanislaw Sulkowski

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Mariola Sulkowska

Medical University of Białystok

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Stanislaw Sulkowski

Medical University of Białystok

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Mariusz Koda

Medical University of Białystok

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Kisielewski W

Medical University of Białystok

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Marek Baltaziak

Medical University of Białystok

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Musiatowicz B

Medical University of Białystok

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Katarzyna Jakubowska

Medical University of Białystok

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Anna Pryczynicz

Medical University of Białystok

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Dziecioł J

Medical University of Białystok

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