ABSTRACTS â ORAL PRESENTATIONS - AMCA, spol. s r.o.
ABSTRACTS â ORAL PRESENTATIONS - AMCA, spol. s r.o.
ABSTRACTS â ORAL PRESENTATIONS - AMCA, spol. s r.o.
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models. As manifested by compromised fertilization parameters, some transgenic boars<br />
of miniature pig line bearing mutated N-terminal part of human huntingtin produce<br />
low quality semen too. Functional spermatozoa mitochondrion plays a substantial role<br />
in oocyte fertilization, therefore the impact of mHtt expression on semen quality and<br />
spermatozoa parameters had been determined using flowcytometry approach.<br />
The mitochondrial mass was estimated by nonyl Acridine Orange (NAO) staining of<br />
cardiolipin. NAO signals do not differ between transgenic (Tg) and wild type (Wt)<br />
spermatozoa. Although defective in motility Tg spermatozoa displayed mitochondrial<br />
membrane potential similar to Wt as assessed by JC-1 staining.<br />
Both Tg and Wt spermatozoa produce ROS spontaneously as determined by MitoSOX TM<br />
Red (MSR) reagent. While there is no difference in maximal levels of MSR signal measured<br />
between Wt and Tg animals, higher ROS production is indicated by sooner development<br />
of detectable MSR signal during Tg spermatozoa staining procedure compared to Wt<br />
spermatozoa.<br />
Acknowledgement<br />
This work was supported by the CHDI Foundation (ID 1035, A5378), The Technical<br />
Agency of the Czech Republic (TA01011466), RVO 67985904, and European Regional<br />
Development Fund CZ.1.05/2.1.00/03.0124.<br />
P10. THE CELL DEATH INDUCED BY TAXANES IN PANCREATIC CANCER CELL LINES<br />
Katerina Kloudova 1,2 , Marie Ehrlichova 1 , Radka Vaclavikova 1 , Veronika Brynychova 1,2 ,<br />
Martin Oliverius 3 , Eva Honsova 3 , Matej Kocik 3 , Iwao Ojima 4 and Pavel Soucek 1<br />
1<br />
Laboratories of Toxicogenomics, National Institute of Public Health in Prague, Czech<br />
Republic; katerina.kloudova@szu.cz<br />
2<br />
3 rd Faculty of Medicine, Charles University in Prague, Czech Republic;<br />
3<br />
Institute for Clinical and Experimental Medicine, Prague, Czech Republic;<br />
4<br />
Institute of Chemical Biology & Drug Discovery and Department of Chemistry, State<br />
University of New York at Stony Brook, New York, USA.<br />
Pancreatic carcinoma is one of the most aggressive tumours with high mortality<br />
worldwide (Jemal et al., 2007). Gemcitabine is primary cytotoxic agent used in the<br />
therapy of pancreatic carcinoma. Unfortunately, treatment with gemcitabine has so far<br />
proved ineffective (Hildago, 2010). Combined therapy together with taxane presents<br />
effort to increase of antitumor effect of gemcitabine (Frese et al., 2012). Taxanes are<br />
successfully used in therapy of various human cancers, mainly of breast and ovarian<br />
carcinomas. However, inherited or acquired resistance of tumour cells to taxanes<br />
(paclitaxel, docetaxel) presents one of the major obstacles in successful therapy. Drug<br />
resistance is a multifactorial process that may be related to drug transport, metabolism<br />
or alterations in apoptosis induction by e.g. taxanes. Certain novel taxanes (i.e. taxanes<br />
of second generation or fluorinated taxanes) possess extremely high potency against<br />
drug-resistant cancer cells expressing the multidrug resistance (MDR) phenotype (Ojima<br />
et al., 1996; Ehrlichova et al., 2012) The aim of our study was to investigate the effect<br />
98 Analytical Cytometry VII