Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Cancer chemotherapy and pharmacology 45 (2000), S. 502-508 
    ISSN: 1432-0843
    Keywords: Key words Malignant mesothelioma ; Chemotherapy ; Gemcitabine ; Irinotecan ; Interleukin-6
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Purpose: The benefits of chemotherapy can be assessed in terms of tumour shrinkage, prolongation of life or simply palliation of symptoms. In the study reported here, in vitro correlates of these parameters were sought as a rational guide to the choice of newer agents in the clinic. Methods: The cytotoxicity and effects on IL-6 production of ten chemotherapy agents representing four different classes of drugs were tested against a panel of five mesothelioma cell lines. Results: The mesothelioma cells were more sensitive to the action of irinotecan (and its active metabolite SN38) and gemcitabine than the control cell lines. Gemcitabine and to a lesser extent irinotecan inhibited the secretion of the proinflammatory cytokine IL-6 at concentrations of each drug that produced only small decreases in cell viability. This effect was not seen in cells treated with docetaxel or vindesine. Higher doses of gemcitabine and irinotecan caused a surge in IL-6 release and this was not due to release of intracellular stores of IL-6 through lysis of the cells. Conclusions: These results suggest that irinotecan and gemcitabine are not only more likely to be active against mesothelioma than other new chemotherapy agents but may also produce a palliative effect in nonresponders to these agents by decreasing the secretion of IL-6.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    ISSN: 1573-6792
    Keywords: Brain Topography ; Statistics ; Evoked Potentials ; Electroencephalography (EEG) ; Positron Emission Tomography (PET) ; Magnetic Resonance Imaging (MRI)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Statistical methods for testing differences between neural images (e.g., PET, MRI or EEG maps) are problematic because they require (1) an untenable assumption of data sphericity and (2) a high subject to electrode ratio. We propose and demonstrate an exact and distribution-free method of significance testing which avoids the sphericity assumption and may be computed for any combination of electrode and subject numbers. While this procedure is rigorously rooted in permutation test theory, it is intuitively comprehensible. The sensitivity of the permutation test to graded changes in dipole location for systematically varying levels of signal/noise ratio, intersubject variability and number of subjects was demonstrated through a simulation of 70 different conditions, generating 5,000 different data sets for each condition. Data sets were simulated from a homogenous single-shell dipole model. For noise levels commonly encountered in evoked potential studies and for situations where the number of subjects was less than the number of electrodes, the permutation test was very sensitive to a change in dipole location of less than 0.75 cm. This method is especially sensitive to localized changes that would be “washed-out‘ by more traditional methods of analysis. It is superior to all previous methods of statistical analysis for comparing topographical maps, because the test is exact, there is no assumption of a multivariate normal distribution or of the correlation structure of the data requiring correction, the test can be tailored to the specific experimental hypotheses rather than allowing the statistical tests to limit the experimental design, and there is no limitation on the number of electrodes that can be simultaneously analyzed.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...