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Abstract: Photodynamic therapy (PDT) is a treatment for cancer involving three key components: sensitizer, light and tissue oxygen. A sensitizer is a chemical compound that can be excited by light of a specific wavelength. Phthalocyanine ClAlPcS2, belonging among the promising second generation of sensitizers, was evaluated as an inducer of photodamage on NIH3T3 (mouse fibroblasts), B16 (mouse melanoma), MCF7 (human breast adenocarcinoma) and G361 (human melanoma) cell lines. A semiconductor laser was used as a source for evocation of the photodynamic effect. We report the influence of various concentrations of the sensitizer in combination with laser irradiation on the photodamage of cells. Viability of cells was determined by means of molecular probes (Calcein AM and ethidium homodimer) for fluorescence microscopy. The quantitative changes of cell viability in relation to sensitizer concentrations and laser irradiation were proved by fluorometric measurement. We detected phototoxicity evoked by laser irradiated sensitizer in all studied cell lines. In addition, the viability studies showed that G361 melanoma cells and MCF7 breast adenocarcinoma cells were more sensitive than NIH3T3 mouse fibroblasts and B16 mouse melanoma to photodynamic damage induced by ClAlPcS2. [Copyright &y& Elsevier] more...

We report the phototoxicity of meso-tetrakis(4-sulphonatophenyl)porphine (TPPS4) and zinc metallocomplex (ZnTPPS4) sensitizers in the presence or absence of 2-hydroxypropyl-β-cyclodextrin (HP-β-CD) on G361human melanoma cells. Morphological changes in cell cultures have been evaluated using inversion fluorescent microscope and image analysis. Viability of cells was determined by means of molecular probes for fluorescence microscopy (LIVE/DEAD kit- double staining with Calcein AM and Ethidium Homodimer). The quantitative changes of cell viability in relation to sensitizers concentrations and irradiation doses were proved by fluorometric measurement with fluoroscan Ascent. We found that the most effective sensitizer is ZnTPPS4 bound to HP-β-CD, since the IC50 value was 12.5 g/ml at the dose of light radiation of 10 J/cm2. [Copyright &y& Elsevier] more...

Eleven macroalgae were collected from the KwaZuluNatal coast and nineteen species from the cooler Western Cape coast in March and April 2000. Ethanolic and aqueous extracts were made and tested for biological activity in the Cox-1 anti-inflammatory assay, in a nematode mortality bioassay for anthelminthic activity, an IC50 anticancer assay and a MIC antimicrobial assay. The ethanolic extracts were very active in the COX-1 anti-inflammatory assay for almost all of the species tested. The aqueous extracts were not active. NO anthelminthic mortality was detected in extracts from any of the species tested, Many of the extracts had cytotoxic activity against three cancer cell lines tested, with those from representative species of the Chlorophyta and Rhodophyta being the most effective. The extracts had much lower cytotoxic activity when tested on normal mouse fibroblasta (NIH3T3). Extracts from only a few species had antimicrobial activity with those of the Chlorophyta tested being the most effective against both the Gram-positive and Gram-negative bacteria [ABSTRACT FROM AUTHOR] more...

Aims: Because of the high prevalence of prostatic cancer and the limitations of its treatment, enormous effort has been put into the development of new therapeutic modalities. One potential tool is the use of cyclin dependent kinase (CDK) inhibitors, which are based on the trisubstituted derivatives of purine. The aim of this study was to analyse alterations of the regulatory pathways in both androgen sensitive and androgen insensitive prostatic cancer cell lines (LNCaP and DU-145, respectively) after blockage of the cell cycle by the synthetic CDK inhibitors, olomoucine and bohemine. Methods: The effects of olomoucine and bohemine were studied on the following parameters: (1) cell proliferation, by measurement of DNA content; (2) viability, by the MTT (3-[4,5-dimethylthiazol-2-yl]2,5-diphenyltetrazolium bromide) and/or XTT (2,3-bis[2-methoxy-4-nitro-5-sulfophenyl]-2H-tetrazolium5-carboxanilide) test; and (3) the expression of p53, pRB, Bcl-2, Bax, pl 6, p21, p27, cyclins A, B, D1, E, p34[sup cdc2], and the androgen receptor (AR), by western blot analysis. Results: Both olomoucine and bohemine were potent inhibitors of growth and viability; however, bohemine was two to three times more effective than olomoucine. The sensitivity of LNCaP cells to both agents was significantly higher. After treatment, both cell lines revealed quite different spectra of protein expression. Conclusions: These results indicate the existence of specific cell cycle regulating pathways in both cell lines, which may be associated with both p53 and AR status. CDK inhibitors exhibited valuable secondary effects on the expression of numerous regulators and thus may modulate the responsiveness of tumour cells to treatment, including treatment with hormone antagonists. [ABSTRACT FROM AUTHOR] more...