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  1. 8 Acta Biochimica Polonica

  2. 5 Cellular and Molecular Biology Letters

  3. 2 Folia Histochemica et Cytobiologica

  4. 2 Polish Journal of Environmental Studies

  5. 1 Acta Biologica Cracoviensia. Series Botanica

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  1. 2 Grieb P.

  2. 2 Skierski J. S.

  3. 1 Anuszewska E. L.

  4. 1 Asici G. S. E.

  5. 1 Bar-Shai M.

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  1. 1 2023

  2. 1 2020

  3. 1 2019

  4. 2 2017

  5. 1 2014

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1

The expression of HSP 27, HSP 70 and HSP 90 in U937 sublines exhibiting different patterns of sensitivity to TNF

100%
Pierzchalski A., Sychowska D., Bartczak M., Bigda J.
Cellular and Molecular Biology Letters
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2002
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tom 07
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nr Suppl.
2

Evaluation of cytotoxicity and pH changes generated by various dental pulp capping materials - an in vitro study

75%
Luczaj-Cepowicz E., Marczuk-Kolada G., Pawinska M., Obidzinska M., Holownia A.
Folia Histochemica et Cytobiologica
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2017
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tom 55
|
nr 2
3

Organometallic iron complexes as potential cancer therapeutics

75%
Mojzisova G., Mojzis J., Vaskova J.
Acta Biochimica Polonica
|
2014
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tom 61
|
nr 4
4

The cytotoxic effect of diphtheria toxin on the actin cytoskeleton

75%
Varol B., Bektas M., Nurten R., Bermek E.
Cellular and Molecular Biology Letters
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2012
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tom 17
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nr 1
Diphtheria toxin (DT) and its N-terminal fragment A (FA) catalyse the transfer of the ADP-ribose moiety of nicotinamide adenine dinucleotide (NAD) into a covalent linkage with eukaryotic elongation factor 2 (eEF2). DT-induced cytotoxicity is versatile, and it includes DNA cleavage and the depolymerisation of actin filaments. The inhibition of the ADP-ribosyltransferase (ADPrT) activity of FA did not affect the deoxyribonuclease activity of FA or its interaction with actin. The toxin entry rate into cells (HUVEC) was determined by measuring the ADP-ribosyltransferase activity. DT uptake was nearly 80% after 30 min. The efficiency was determined as Km = 2.2 nM; Vmax = 0.25 pmol.min−1. The nuclease activity was tested with hyperchromicity experiments, and it was concluded that G-actin has an inhibitory effect on DT nuclease activity. In thepresence of DT and mutant of diphtheria toxin (CRM197), F-actin depolymerisation was determined with gel filtration, WB and fluorescence techniques. In the presence of DT and CRM197, 60–65% F-actin depolymerisation was observed. An in vitro FA-actin interaction and F-actin depolymerisation were reported in our previous paper. The present study thus confirms the depolymerisation of actin cytoskeleton in vivo.
5

The receptors regulating natural cytotoxic effector functions

75%
Nikolova M., Boumsell L., Bensussan A.
Archivum Immunologiae et Therapiae Experimentalis
|
2001
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tom 49
|
nr 2
6

Cytotoxic effects of cladribine and tezacitabine toward HL-60

75%
Stachnik K., Grieb P., Skierski J. S.
Acta Biochimica Polonica
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2005
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tom 52
|
nr 2
The aim of the study was to determine the relation between the cytotoxic and cytostatic effects of tezacitabine and cladribine on a HL-60 cell line and the time of exposure of cells to these drugs. Cell viability and induction of apoptosis were assessed using flow cytometry methods. Apoptosis was confirmed by direct microscopic observation. Growth inhibition was examined by cell counting. After 24 h incubation tezacitabine was equally or less toxic compared to cladribine. However, toxicity of tezacitabine strongly rose after 48 h incubation leading to massive cell death at doses much lower than those of cladribine. Assessment of the effect of increased exposure time on the clinical efficacy of tezacitabine is indicated.
7
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Content available

Blood platelet secretory activity in the course of giardiosis

75%
Matowicka-Karna J., Panasiuk A.
Wiadomości Parazytologiczne
|
1998
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tom 44
|
nr 3
8

Cytotoxic effects of staphylococcal leukocidins on isolated fish macrophages and lymphocytes in vitro

75%
Bownik A., Siwicki A. K., Szmigielski S., Sobiczewska E., Prevost G., Monteil H., Colin D. A., Studnicka M., Jeljaszewicz J.
Bulletin of the Polish Academy of Sciences. Biological Sciences
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2000
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tom 48
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nr 2
9

Metabolism and cytotoxic effects of 2-chloroadenine, the major catabolite of 2-chloro-2'-deoxyadenosine

75%
Bontemps F., Delacauw A., Cardoen S., Van Den Neste E., Van Den Berghe G.
Cellular and Molecular Biology Letters
|
1999
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tom 04
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nr 3
10
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Content available

Cytotoxic effect of organic dust extracts from different working environments: an in vitro assay

75%
Roepstorff V., Sigsgaard T.
Annals of Agricultural and Environmental Medicine
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1997
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tom 04
|
nr 2
11

Amoebicidal and amoebistatic effects of Artemisia argyi methanolic extracts on Acanthamoeba castellanii trophozoites and cysts

63%
Koloren O., Koloren Z., Sekeroglu Z. A., Colayvaz M., Karanis P.
Acta Parasitologica
|
2019
|
tom 64
|
nr 1
12

Cytotoxic and apoptotic effect of nanoclinoptilolite on canine osteosarcoma cell lines

63%
Ulutas P. A., Kiral F., Ulutas B., Asici G. S. E.
Journal of Veterinary Research
|
2020
|
tom 64
|
nr 4
13

Caspase-3 as an important factor in the early cytotoxic effect of nickel on oral mucosa cells in patients treated orthodontically

63%
Buczko P., Szarmach I., Grycz M., Kasacka I.
Folia Histochemica et Cytobiologica
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2017
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tom 55
|
nr 1
14

Use of cultured cells of mammal and insect origin to assess cytotoxic effects of the pesticide Chlorpyrifos

63%
Pollakova J., Pistl J., Kovalkovicova N., Csank T., Kocisova A., Legath J.
Polish Journal of Environmental Studies
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2012
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tom 21
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nr 4
In the present study four different cell cultures, derived from rabbit kidney (RK13), rat, and murine liver (WBF344 and Hepa 1c1c7) and insect origin (Sf21) were used to examine the effects of chlorpyrifos. Sf21 cells were the most sensitive to chlorpyrifos, with significant suppression of their proliferative activity ranging from 10⁻¹-10⁻⁵ M. However, significant suppression of proliferative activity also was recorded in mammalian cell cultures Hepa 1c1c7 (10⁻¹-10⁻³ M), WBF344 (10⁻¹-10⁻² M), and RK13 ( 10⁻¹ M). A cytopathic effect and LDH leakage into the medium was observed in RK 13 ( 10⁻¹-10⁻³ M) > WBF344 and Hepa 1c1c7 cells ( 10⁻¹-10⁻² M) > Sf21 ( 10⁻¹ M) compared to solvent control. Our results indicate that chlorpyrifos exposure caused a species-dependent decrease in cell proliferation and cell membrane damage.
15
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Content available

Exploring the potential of Inula viscosa extracts for antioxidant, antiproliferative and apoptotic effects on human liver cancer cells and a molecular docking study

63%
Kheyar-Kraouche N., Boucheffa S., Bellik Y., Farida K., Brahmi-Chendouh N.
BioTechnologia. Journal of Biotechnology Computational Biology and Bionanotechnology
|
2023
|
tom 104
|
nr 2
16

Cytotoxic and mutagenic effects of hydrogen peroxide in murine L5178Y sublines

63%
Kruszewski M., Szumiel I.
Acta Biochimica Polonica
|
1993
|
tom 40
|
nr 1
17

The effect of melatonin on the cytotoxic effects of doxorubicin on the myocardium and on transplantable Morris hepatoma in rats

63%
Dziegiel P., Podhorska-Okolow M., Surowiak P., Ciesielska U., Rabczynski J., Zabel M.
Cellular and Molecular Biology Letters
|
2002
|
tom 07
|
nr Suppl.
18

Studies on the nature of genotoxic and cytotoxic effects induced by hydralazine

63%
Marczewska J., Koziorowska J. H.
Acta Biochimica Polonica
|
1997
|
tom 44
|
nr 2
The nature of genotoxic and cytotoxic effects induced by hydralazine was analyzed taking into account possible protection of cells by catalase, superoxide dismutase and dimethyl sulfoxide. For the experiments designed to evaluate the influence of scavengers on the genotoxicity expressed as the SOS induction factor the E. coli PQ37 strain was used. The cytotoxic effects were investigated in V3 cells cultured in vitro. The genotoxicity and cytotoxicity of hydralazine were suppressed by catalase in a dose-dependent manner but they were enhanced by superoxide dismutase. No protective effect of dimethyl sulfoxide was observed. Our results indicate that H2O2 plays an essential role in the genotoxicity and cytotoxicity of hydralazine.
19

Pioglitazone, a PPAR-gamma ligand, exerts cytostatic-cytotoxic effects against cancer cells, that do not result from inhibition of proteasome

63%
Mrowka P., Glodkowska E., Mlynarczuk-Bialy I., Bialy L., Kuckelkorn U., Nowis D., Makowski M., Legat M., Golab J.
Acta Biochimica Polonica
|
2008
|
tom 55
|
nr 1
Thiazolidinediones are oral antidiabetic agents that activate peroxisome proliferator-activated receptor-gamma (PPAR-γ) and exert potent antioxidant and anti-inflammatory properties. It has also been shown that PPAR-γ agonists induce G0/G1 arrest and apoptosis of malignant cells. Some of these effects have been suggested to result from inhibition of proteasome activity in target cells. The aim of our studies was to critically evaluate the cytostatic/cytotoxic effects of one of thiazolidinediones (pioglitazone) and its influence on proteasome activity. Pioglitazone exerted dose-dependent cytostatic/cytotoxic effects in MIA PaCa-2 cells. Incubation of tumor cells with pioglitazone resulted in increased levels of p53 and p27 and decreased levels of cyclin D1. Accumulation of polyubiquitinated proteins within cells incubated with pioglitazone suggested dysfunction of proteasome activity. However, we did not observe any influence of pioglitazone on the activity of isolated proteasome and on the proteolytic activity in lysates of pioglitazone-treated MIA PaCa-2 cells. Further, treatment with pioglitazone did not cause an accumulation of fluorescent proteasome substrates in transfected HeLa cells expressing unstable GFP variants. Our results indicate that pioglitazone does not act as a direct or indirect proteasome inhibitor.
20

Cytotoxic effect of nitric oxide on human hematological malignant cells

63%
Tsumori M., Tanaka J., Koshimura K., Kawaguchi M., Murakami Y., Kato Y.
Acta Biochimica Polonica
|
2002
|
tom 49
|
nr 1
We investigated the cytotoxic effect of nitric oxide (NO) on primary culture of human hematological malignant cells. Sodium nitroprusside (SNP), an NO donor, had cytotoxic effects on the cells of some patients with malignant lymphoma (ML), acute myelocytic leukemia (AML) or chronic myelomonocytic leukemia (CMMoL), but not with multiple myeloma. Cultured cells from the ML patient remained sensitive to SNP after the cells became resistant to anti-cancer drugs. In contrast, the cells from the pa­tients with AML and CMMoL became resistant to SNP while anti-cancer drugs re­mained effective. In samples of the cells of the patients with ML and AML, the number of CD3 positive lymphoma cell was decreased by SNP and the number of CD33 nega­tive cells and normal B lymphocytes (CD19 positive cells) were increased. In the cells of the patient with ML, apoptosis was induced by SNP. SNP had no effect on lympho­cytes of healthy volunteers. These results suggest that SNP had an anti-tumor effect on human hematological malignant cells.
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