http://dspace.nbuv.gov.ua:80/handle/123456789/133119 2026-04-17T23:28:43Z http://dspace.nbuv.gov.ua:80/handle/123456789/135114 Influence of two pt(iv) complexes on viability, apoptosis and cell cycle of B16 mouse melanoma tumors Kaznica, A.; Drewa, T.; Lakomska, I.; Ryta-Stamirowska, P.; Debski, R.; Styczynski, J.; Drewa, G.; Szłyk, E. Several platinum(IV) complexes are showing considerable promise in initial trials, producing reactive intermediates that then interact with DNA. Aim: To perform in vitro study of two new platinum(IV) complexes cytotoxic effect on B16 mouse melanoma cells. Methods: PtCl₄ (dbtp)₂ and PtCl₂ (6mp)₂ complexes were prepared. PtCl₄ (dbtp)₂ was created as modification of PtCl₄ (dmtp) test previously.Apoptosis and necrosis were examined using flow cytometry, upon Annexin V/PI staining. Results: LC₁₀,LC₅₀ andLC₉₀ parameters established for PtCl₄ (dbtp)₂ were as following: 2.6, 17.0, 58.0 μmol/L. However LC₁₀ andLC₅₀ established for PtCl₂ (6mp)₂ were 1.2 and 14.0μmol/l respectively. The both complexes induced apoptosis. PtCl₂ (6mp)₂ induced cell cycle arrest in G0/G1, while PtCl₄ (dbtp)₂ — in S-phase. Conclusions: PtCl₄ (dbtp)₂ appeared to be more cytotoxic against B16 cells than PtCl₂ (6mp)₂ . Apoptosis was the main mechanism of cell loss in cultures incubated with both tested complexes. 2009-01-01T00:00:00Z http://dspace.nbuv.gov.ua:80/handle/123456789/135113 Polymorphisms of the dna base excision repair gene mutyh in head and neck cancer Sliwinski, T.; Markiewicz, L.; Rusin, P.; Pietruszewska, W.; Olszewski, J.; Morawiec-Sztandera, A.; Mlynarski, W.; Majsterek, I. Background: Head and neck squamous cell carcinomas (HNSCC) comprise about 6% of all malignant neoplasms. The major risk factors of HNSCC are smoking and alcohol consumption. Genetic polymorphisms of DNA repair enzymes may lead to genetic instability and carcinogenesis. MUTYH gene encodes a DNA glycosylase that can initiate the base excision repair (BER) pathway and prevent G:C > T:A transversion by excising adenine mispaired with 8-hydroxyguanine produced by reactive oxygen species (ROS). Aim: to perform a case-control study to test the association between polymorphism in the MUTYH gene: Tyr165Cys and head and neck cancer risk progression. Methods: Genotypes were determined in DNA from peripheral blood lymphocytes of 193 patients (among them 97 subjects with precancerous hyperplastic laryngeal lesions and 96 subjects with head and neck cancer) and 140 age, sex and ethnic-matched cancer-free controls by tetra-primer amplification refractory mutation system PCR (T-ARMS-PCR). Results: We found an association between head and neck cancer risk and the Tyr165Tyr variant of the MUTYH gene (OR 2.18; 95% CI 1.19–3.97). For Tyr165Tyr genotype we also observed positive correlation with cancer progression assessed by tumor size (OR 4.56; 95% CI 1.60–12.95). We did not observe any correlation between Tyr165Cys polymorphism of MUTYHgene and precancerous hyperplastic laryngeal lesions risk. Conclusion: The Tyr165Tyr polymorphic variant of the MUTYHgene may be associated with head and neck cancer in Polish population. 2009-01-01T00:00:00Z http://dspace.nbuv.gov.ua:80/handle/123456789/135111 Tyrosine kinase inhibitors in treatment of fibrous histiocytoma Maur, D.; Panou, C.; Valachis, A.; Kamposioras, K.; Tsali, L. Aim: To describe potential beneficial effects of tyrosine kinase inhibitor in the treatment of unresectable/metastatic fibrous histiocytoma. Methods: We report a case of advanced stage fibrous histiocytoma with locally recurrent disease plus lung and bone metastatic deposits. Patient was treated with the tyrosine kinase inhibitor sunitinib. Results: Treatment with Sunitinib resulted in disease stabilization in the regional lesion and in good partial response for metastatic foci (reduction in number and size). After 13 months of treatment the patient is doing well with no tumor progression. Conclusions: This case appears to be one of the first documentations of beneficial effect and potential long-term benefit of TKIs in the treatment of fibrous histiocytoma. 2009-01-01T00:00:00Z http://dspace.nbuv.gov.ua:80/handle/123456789/135107 Limiting effect of diazepam on lewis lung carcinoma metastasis in anxious male mice Kaledin, V.I.; llnitskaya, S.I.; Nikolin, V.P.; Popova, N.A.; Smagin, D.A.; Kudryavtseva, N.N. Aim: It has been shown previously that chronic social defeat stress produces development ofstrong anxiety and increases intensity of experimental metastasis in the losers in comparison with the winners and control mice. The question was: isit possible to decrease the number ofmetastases inthe losers by chronic or acute diazepam treatment. Materials and Methods: Sensory contact model was used for generating male mice with repeated experience of social victories or defeats in daily agonistic interactions. Tumor cells of Lewis Lung Carcinoma (LLC) were injected into the tail vein of animals after 10 days of agonistic interactions. Then mice were treated acutely or chronically (7 days) with diazepam (1 mg/kg, i. p). Number ofmetastases in the lung was calculated in 16 days after tumor cell transplantation. Results: Diazepam decreased the number of LLC metastases in anxious losers, whereas in the winners and control mice, without anxiety state, diazepam was ineffective. Conclusion: Well-known anxiolytic diazepam may decrease intensity of metastasis in anxious mice. 2009-01-01T00:00:00Z