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1.
Genes (Basel) ; 12(5)2021 05 13.
Article in English | MEDLINE | ID: mdl-34068126

ABSTRACT

An association between the cancer invasive activities of cells and their exposure to advanced glycation end-products (AGEs) was described early in some reports. An incubation of cells with BSA-AGE (bovine serum albumin-AGE), BSA-carboxymethyllysine and BSA-methylglyoxal (BSA-MG) resulted in a significant increase in DNA damage. We examined the genotoxic activity of new products synthesized under nonaqueous conditions. These were high molecular mass MAGEs (HMW-MAGEs) formed from protein and melibiose and low molecular mass MAGEs (LMW-MAGEs) obtained from the melibiose and N-α-acetyllysine and N-α-acetylarginine. We have observed by measuring of micronuclei in human lymphocytes in vitro that the studied HMW-MAGEs expressed the genotoxicity. The number of micronuclei (MN) in lymphocytes reached 40.22 ± 5.34 promille (MN/1000CBL), compared to 28.80 ± 6.50 MN/1000 CBL for the reference BSA-MG, whereas a control value was 20.66 ± 1.39 MN/1000CBL. However, the LMW-MAGE fractions did not induce micronuclei formation in the culture of lymphocytes and partially protected DNA against damage in the cells irradiated with X-ray. Human melanoma and all other studied cells, such as bronchial epithelial cells, lung cancer cells and colorectal cancer cells, are susceptible to the genotoxic effects of HMW-MAGEs. The LMW-MAGEs are not genotoxic, while they inhibit HMW-MAGE genotoxic activity. With regard to apoptosis, it is induced with the HMW-MAGE compounds, in the p53 independent way, whereas the low molecular mass product inhibits the apoptosis induction. Further investigations will potentially indicate beneficial apoptotic effect on cancer cells.


Subject(s)
Apoptosis , Glycation End Products, Advanced/toxicity , Micronuclei, Chromosome-Defective/drug effects , Arginine/analogs & derivatives , Cells, Cultured , DNA Damage , Glycation End Products, Advanced/chemical synthesis , Humans , Lymphocytes/drug effects , Lymphocytes/radiation effects , Lysine/analogs & derivatives , Melibiose/chemistry , Micronucleus Tests , X-Rays
2.
Contemp Oncol (Pozn) ; 20(6): 449-452, 2016.
Article in English | MEDLINE | ID: mdl-28239281

ABSTRACT

Current cancer radiotherapy relies on increasingly high dose rates of ionising radiation (100-2400 cGy/min). It is possible that changing dose rates is not paralleled by treatment effectiveness. Irradiating cancer cells is assumed to induce molecular alterations that ultimately lead to apoptotic death. Studies comparing the efficacy of radiation-induced DNA damage and apoptotic death in relation to varying dose rates do not provide unequivocal data. Whereas some have demonstrated higher dose rates (single dose) to effectively kill cancer cells, others claim the opposite. Recent gene expression studies in cells subject to variable dose rates stress alterations in molecular signalling, especially in the expression of genes linked to cell survival, immune response, and tumour progression. Novel irradiation techniques of modern cancer treatment do not rely anymore on maintaining absolute constancy of dose rates during radiation emission: instead, timing and exposure areas are regulated temporally and spatially by modulating the dose rate and beam shape. Such conditions may be reflected in tumour cells' response to irradiation, and this is supported by the references provided.

3.
Food Chem ; 168: 546-53, 2015 Feb 01.
Article in English | MEDLINE | ID: mdl-25172746

ABSTRACT

The antioxidant and radioprotective effects of the phenolic glycosides from Capsicum annuum L. were examined. There were: sinapoyl-E-glucoside, quercetin-3-O-rhamnoside-7-O-glucoside, quercetin-3-O-rhamnoside and luteolin-7-O-(2-apiosyl)-glucoside. To the best of our knowledge, this is the first study to assay these compounds for their radioprotective effect on human cell lymphocytes in response to oxidative damage induced by X radiation and their antioxidant abilities. Investigated compounds showed weaker antiradical activities, but their radioprotective potentials were higher than those of their aglycones. Quercetin-3-O-rhamnoside showed the highest radioprotective activity (50% according to control). Furthermore, quercetin and luteolin derivatives, in contrast to free aglycones, were not cytotoxic against human lymphocytes for all concentrations tested. The best correlation between radioprotective and antiradical activities of the investigated compounds was observed in the relationship to O2(-) generated using the NADH/PMS method (R(2)=0.859). Thus, we propose that superoxide radical scavenging activity is a useful method for screening for compounds with promising radioprotective potential.


Subject(s)
Antioxidants/pharmacology , Capsicum/chemistry , Glycosides/chemistry , Lymphocytes/drug effects , Oxidative Stress/drug effects , Phenols/pharmacology , Protective Agents/pharmacology , Antioxidants/chemistry , Antioxidants/isolation & purification , Capsicum/metabolism , Chromatography, High Pressure Liquid , Fruit/chemistry , Fruit/metabolism , Glycosides/isolation & purification , Glycosides/pharmacology , Humans , Lymphocytes/radiation effects , Oxidative Stress/radiation effects , Phenols/chemistry , Phenols/isolation & purification , Protective Agents/chemistry , Protective Agents/isolation & purification , X-Rays
4.
Acta Biochim Pol ; 59(4): 627-30, 2012.
Article in English | MEDLINE | ID: mdl-23189278

ABSTRACT

Vitamin D3 (1,25(OH)2D3 (1,25-dihydroxyvitamin D3)) is a hormone playing a crucial role in numerous biological processes in the human body, including induction and control of cell proliferation and differentiation. Numerous data relate the vitamin D3 level with various types of cancer. It has been suggested that SNPs in the vitamin D3 receptor (VDR) gene might influence both the risk of cancer occurrence and cancer progression. The aim of this study was to search for genetic correlations between individual SNPs in the VDR gene and the risk of oral cavity carcinoma. Two SNPs were selected based on the literature and our previous results. Seventy-three patients with squamous cell carcinoma of the head and neck and one hundred control subjects were investigated. Two SNPs in the VDR gene were genotyped in minisequencing reactions followed by capillary electrophoresis. Hardy-Weinberg equilibrium (HWE), the χ(2) test and logistic regression were used for statistical analysis. The SNP rs2238135 in the VDR gene displayed statistical differences in frequency between the tested groups (p=0,0007). Furthermore, the G/C genotype of the rs2238135 in the VDR gene was characterized by a 3.16 fold increased risk of oral cavity carcinoma. The obtained results provide evidence for a genetic association between rs2238135 in the VDR gene and the occurrence and risk of oral cavity cancer.


Subject(s)
Carcinoma, Squamous Cell , Mouth Neoplasms/genetics , Mouth , Receptors, Calcitriol/genetics , Adult , Carcinoma, Squamous Cell/genetics , Carcinoma, Squamous Cell/pathology , Cholecalciferol/genetics , Cholecalciferol/metabolism , Female , Genetic Association Studies , Genotype , Humans , Male , Mouth/metabolism , Mouth/pathology , Mouth Neoplasms/pathology , Polymorphism, Single Nucleotide , Risk Factors
5.
Rep Pract Oncol Radiother ; 16(6): 256-61, 2011.
Article in English | MEDLINE | ID: mdl-24376990

ABSTRACT

BACKGROUND: The biological effects of ionizing radiation have long been thought to results from direct targeting of the nucleus leading to DNA damage. Over the years, a number of non-targeted or epigenetic effects of radiation exposure have been reported where genetic damage occurs in cells that are not directly irradiated but respond to signals transmitted from irradiated cells, a phenomenon termed the "bystander effects". AIM: We compared the direct and bystander responses of human A 549, BEAS-2-B and NHDF cell lines exposed to both photon (6 MV) and electron (22 MeV) radiation inside a water phantom. The cultures were directly irradiated or exposed to scattered radiation 4 cm outside the field. In parallel, non-irradiated cells (termed bystander cells) were incubated in ICM (irradiation conditioned medium) collected from another pool of irradiated cells (termed donor cells). MATERIALS AND METHODS: In directly irradiated cells as well as ICM-treated cells, the frequency of micronuclei and condensation of chromatin characteristic for the apoptotic process were estimated using the cytokinesis-block micronucleus test. RESULTS: In all tested cell lines, radiation induced apoptosis and formation of micronuclei. A549 and BEAS-2B cells cultured in ICM showed increased levels of micronuclei and apoptosis, whereas normal human fibroblasts (NHDF line) were resistant to bystander response. In A549 and BEAS-2B cells placed outside the radiation field and exposed to scattered radiation the formation of micronuclei and induction of apoptosis were similar to that after ICM-treatment. CONCLUSION: Results suggest that the genetic damage in cells exposed to scattered radiation is caused by factors released by irradiated cells into the medium rather than by DNA damage induced directly by X rays. It seems that bystander effects may have important clinical implications for health risk after low level radiation exposure of cells lying outside the radiation field during clinical treatment.

6.
Int J Radiat Oncol Biol Phys ; 77(1): 244-52, 2010 May 01.
Article in English | MEDLINE | ID: mdl-20394856

ABSTRACT

PURPOSE: Cells exposed to ionizing radiation release factors that induce deoxyribonucleic acid damage, chromosomal instability, apoptosis, and changes in the proliferation rate of neighboring unexposed cells, phenomena known as bystander effects. This work analyzes and compares changes in global transcript levels induced by direct irradiation and by bystander effects in K562 (human erythroleukemia) cells. METHODS AND MATERIALS: Cells were X-irradiated with 4 Gy or transferred into culture medium collected from cells 1 h after irradiation (irradiation-conditioned medium). Global transcript profiles were assessed after 36 h of growth by use of Affymetrix microarrays (Affymetrix, Santa Clara, CA) and the kinetics of change of selected transcripts by quantitative reverse transcriptase-polymerase chain reaction. RESULTS: The level of the majority (72%) of transcripts changed similarly (increase, decrease, or no change) in cells grown in irradiation-conditioned medium or irradiated, whereas only 0.6% showed an opposite response. Transcript level changes in bystander and irradiated cells were significantly different from those in untreated cells grown for the same amount of time and were confirmed by quantitative reverse transcriptase-polymerase chain reaction for selected genes. Signaling pathways in which the highest number of transcripts changed in both conditions were found in the following groups: neuroactive ligand-receptor, cytokine-cytokine receptor interaction, Janus Kinase-Signal Transducers and Activators of Transcription (JAK-STAT) and Mitogen-Activated Protein Kinase (MAPK) In control cells more transcripts were downregulated than in irradiated and bystander cells with transcription factors YBX1 and STAT5B, heat shock protein HSPA1A, and ribonucleic acid helicase DDX3X as examples. CONCLUSIONS: The transcriptomes of cells grown in medium from X-irradiated cells or directly irradiated show very similar changes. Signals released by irradiated cells may cause changes in the transcriptome of neighboring cells that sustain their survival.


Subject(s)
Bystander Effect/radiation effects , Culture Media, Conditioned/pharmacology , Gene Expression Profiling/methods , K562 Cells/radiation effects , Signal Transduction/radiation effects , Bystander Effect/drug effects , DNA Damage , Down-Regulation , Humans , K562 Cells/metabolism , Radiation Dosage , Reverse Transcriptase Polymerase Chain Reaction/methods , Signal Transduction/drug effects , Time Factors , Up-Regulation
7.
Endokrynol Pol ; 57 Suppl A: 45-51, 2006.
Article in Polish | MEDLINE | ID: mdl-17091456

ABSTRACT

INTRODUCTION: The aim of the study was estimation of occurrence of SNP (single nucleotide polymorphism) sites in LGALS3BP gene in patients with benign and malignant thyroid tumors and analysis of correlation between their frequency and the histological type of thyroid lesions. MATERIAL AND METHODS: The studied group consisted of 58 patients, 24 with papillary thyroid carcinomas, 19 with nodular goiters and 15 with follicular adenomas. Control group included 180 healthy volunteers. Four different SNP polymorphisms were analysed in PCR products using the SNaPshot test, on genetic analyser ABI Prism 310; these can be found in NCBI database under rs numbers: 1803938 (a/g), 11024 (g/c), 1801463 (a/c) and 1131516 (c/t). RESULTS: In all patients analysis of SNP sites revealed: lack of polymorphism in a/g rs 18039380; polymorphism identical to database in g/c rs 11024 and polymorphism different from database in a/g rs 1801463 and c/g rs 131516. There were no significant differences between patients with thyroid lesions and group of healthy controls. CONCLUSION: Single nucleotide polymorphism (SNP) of LGALS3BP gene (found in NCBI) database are not characteristic for papillary thyroid cancer, follicular adenomas and nodular goiter.


Subject(s)
Adenoma/genetics , Antigens, Neoplasm/genetics , Biomarkers, Tumor/genetics , Carrier Proteins/genetics , Glycoproteins/genetics , Goiter, Nodular/genetics , Polymorphism, Single Nucleotide , Thyroid Neoplasms/genetics , Adult , Aged , Case-Control Studies , Female , Humans , Male , Middle Aged
8.
Pol J Microbiol ; 54 Suppl: 47-52, 2005.
Article in English | MEDLINE | ID: mdl-16457380

ABSTRACT

This study investigates the toxic effect of E(2)nonenal (trans-2-nonenal, T2N) and its conjugate with horse muscle myoglobin (Mb) tested on murine cell line L929 and human cell line A549, as well as the genotoxic effect of these compounds assayed by measuring of micronuclei in human cells K562. It is an aldehyde, which is occurring as the substance responsible for an off flavour in aged beers, but originates also from lipid oxidation in heat processed food. T2N is an aldehyde formed from linoleic acid as a secondary oxidation product. The modification of Mb with T2N was analyzed with the use of SDS-polyacrylamide gel electrophoresis (SDS-PAGE), and electrospray ionization mass spectrometry (ESI-MS). Results from SDS-PAGE suggest that T2N substitutes Mb and additionally causes cross-linking with polymerization of Mb resulting in an insoluble fraction. The ESI-MS spectrum of the soluble fraction used in the toxicity tests, demonstrated that conjugation of T2N with Mb yielded Mb adducts with one residue of trans-2-nonenal per myoglobin molecule as the major fraction and adducts with different numbers of T2N molecules as minor fractions. In the cytotoxicity assay the T2N and its Mb conjugate causes 50% destruction of cells at the concentration 95-125 microg/ml and 200 microg/ml respectively, when L929 and A549 cell lines were used, whereas Mb control tested up to 2000 mg/ml was without any cytotoxic effect. In genotoxicity in vitro assay we have observed that the T2N and its Mb conjugate expressed the genotoxicity. The number of micronuclei in human K562 cells reached 26 +/- 2.16 promille (MN/1000 cells), comparing to 62 +/- 8.64 MN/1000 cells for the reference free T2N, whereas a control value was 10.33 +/- 1.25 MN/1000 cells. The studied compounds expressed also the apoptotic effect in K562 cells as the number of apoptotic cells increased to 44.67 +/- 4.92 promille for T2N-Mb, comparing to 168.67 +/- 37.28 promille for free T2N, whereas a control value was 30.33 +/- 1.36 promille for Mb. In these assays the T2N-Mb conjugate is several times more toxic in relation to control protein. Results indicate that T2N adducts with protein are potent to induce various cytotoxic and apoptotic effects when assayed in vitro tests. It suggests that higher level of such aldehyde might create in organism severe potential of toxicity.


Subject(s)
Aldehydes/toxicity , Beer , Cytotoxins/toxicity , Lipid Peroxidation , Mutagens/toxicity , Aldehydes/chemistry , Animals , Apoptosis , Cell Line , Electrophoresis, Polyacrylamide Gel , Food Preservation , Hot Temperature , Humans , Mice , Micronucleus Tests , Myoglobin/chemistry , Spectrometry, Mass, Electrospray Ionization
9.
Acta Biochim Pol ; 51(3): 839-43, 2004.
Article in English | MEDLINE | ID: mdl-15448744

ABSTRACT

The effects of thiamine (vitamin B1) on the level of spontaneous or radiation-induced genetic changes in human lymphocytes in vitro were studied. Cultured lymphocytes were exposed to increasing concentrations of thiamine (0-500 microg/ml) and irradiated with X-rays. The DNA damage was estimated as the frequency of micronuclei and apoptotic or necrotic morphological changes in fixed cells. The results show that thiamine alone did not induce genetic changes. A significant decrease in the fraction of apoptotic and necrotic cells was observed in lymphocytes irradiated in the presence of vitamin B1 at concentrations between 1-100 microg/ml compared to those irradiated in the absence of thiamine. Vitamin B1 at 1 and 10 microg/ml decreased also the extent of radiation-induced formation of micronuclei. Vitamin B1 had no effect on radiation-induced cytotoxicity as measured by nuclear division index. The results indicate that vitamin B1 protects human cells from radiation-induced genetic changes.


Subject(s)
Lymphocytes/drug effects , Lymphocytes/radiation effects , Thiamine/pharmacology , Apoptosis/drug effects , Apoptosis/radiation effects , Cell Nucleus Division/drug effects , Cell Nucleus Division/radiation effects , DNA Damage , Humans , In Vitro Techniques , Lymphocytes/metabolism , Lymphocytes/pathology , Micronucleus Tests , Necrosis
10.
Cell Mol Biol Lett ; 9(1): 153-65, 2004.
Article in English | MEDLINE | ID: mdl-15048159

ABSTRACT

In our previous study, a 454 bp DNA fragment was isolated from rat genomic DNA as an element which interacts with nuclear matrix proteins, i.e. a Matrix Associated Region (MAR). Computer analyses revealed that the right half of this fragment, named RME (Rat MAR Element), possesses a high matrix association potential and is likely to be responsible for the matrix association of the whole sequence. RME was used as a probe in an electrophoretic mobility shift assay (EMSA), and with the use of Southwestern blotting, a rat liver nuclear protein which binds specifically to it was identified. Its molecular mass was estimated by SDS-PAGE as 30 kDa (p30). Polyclonal antibodies raised against protein-RME complexes caused a super-shift of specific complexes in EMSA, and bound to p30 in nuclear extracts of rat liver in Western blotting. The immunofluorescence labelling of a rat embryonic fibroblast cell monolayer with anti-p30 antibody revealed a mainly intranuclear pattern of staining.


Subject(s)
Cell Nucleus/genetics , DNA-Binding Proteins/genetics , Matrix Attachment Regions/genetics , Nuclear Matrix/genetics , Nuclear Proteins/genetics , Animals , Cell Nucleus/metabolism , Cells, Cultured , Chromatin/genetics , Chromatin/metabolism , DNA-Binding Proteins/metabolism , Electrophoretic Mobility Shift Assay , Fibroblasts/metabolism , Liver/metabolism , Nuclear Matrix/metabolism , Nuclear Proteins/metabolism , Rats
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