1,721,003 research outputs found
Proteomics as a tool to disclose the cellular and molecular mechanisms of selected anticancer gold compounds
Gold compounds form an attractive class of cytotoxic metal compounds of potential application as anticancer agents. Notably, the mode of action of cytotoxic gold compounds appears to differ from that of the widely used anticancer Pt drugs -to which they were initially inspired- and to be basically DNA-independent. However, mechanistic details are still largely lacking for this class of metal-based drugs. To shed light on these issues we have developed a proteomic strategy that is capable of highlighting the perturbations in protein expression elicited by gold drugs in a selected cancer cell line with the final aim to disclose the underlying molecular mechanisms. In recent years, this type of strategy has been systematically applied, in our laboratory, to a representative panel of gold compounds including seven outstanding cytotoxic agents, i.e. six experimental gold(III) and gold(I) compounds and the clinical gold(I) drug, auranofin. A2780 human ovarian cancer cells were used as the standard cellular model for these studies. Proteins differentially expressed upon treatment were separated by 2-DE and identified by MALDI TOF and their meaning tentatively assessed through bioinformatic analysis. The occurrence of various and often overlapping molecular mechanisms was revealed. The affected proteins were found to belong -in most cases- to redox control systems and/or to the proteasome machinery implying that the severe cellular damage induced by gold compounds predominantly originates at these two distinct levels. However, for one Au(III) and one Au(I) compound, i.e. [(bipydmb-H)Au(OH)][PF6] (bipydmb-H = deprotonated 6-(1,1-dimethylbenzyl)-2,2′-bipyridine) (Aubipyc) and the bis(1-butyl-3-methyl-imidazole-2-ylidene) gold(I) [Au(NHC)2]PF6, a substantially greater number of proteomic alterations were detected pointing out, in both cases, to glucose metabolism as an additional target process of the cytotoxic action. The results that were obtained with the seven gold complexes are discussed in the frame of the available knowledge on anticancer gold drugs and their mechanisms. In general, our studies underscore the large amount of information that proteomic measurements may provide on the mode of action of metal-based drugs at the cellular level and delineate a very effective methodology for the identification of the respective cytotoxic mechanisms. We propose that the interpretation of the proteomic data in terms of the main affected cellular processes is further supported and validated through the implementation of complementary metabolomics and metallomics experiments
Going Beyond Counting First Authors in Author Co-citation Analysis
The present study examines one of the fundamental aspects of author co-citation analysis (ACA) - the way co-citation
counts are defined. Co-citation counting provides the data on which all subsequent statistical analyses and mappings
are based, and we compare ACA results based on two different types of co-citation counting - the traditional type that
only counts the first one among a cited work's authors on the one hand and a non-traditional type that takes into
account the first 5 authors of a cited work on the other hand. Results indicate that the picture produced through this non-traditional author co-citation counting contains more coherent author groups and is therefore considerably clearer. However, this picture represents fewer specialties in the research field being studied than that produced through the traditional first-author co-citation counting when the same number of top-ranked authors is selected and analyzed. Reasons for these effects are discussed
Variations on the Author
“Variations on the Author” discusses two of Eduardo Coutinho’s recent films (Um Dia na Vida, from 2010, and Últimas Conversas, posthumously released in 2015) and their contribution to the general question of documentary authorship. The director’s filmography is characterized by a consistent yet self-effacing form of authorial self-inscription: Coutinho often features as an interviewer that rather than express opinions propels discourses; an interviewer that is good at listening. This mode of self-inscription characterizes him as an author who is not expressive but who is nonetheless markedly present on the screen. In Um Dia na Vida, however, Coutinho is completely absent form the image, while Últimas Conversas, on the contrary, includes a confessional prologue that moves the director from the margins to the center of his films. This article examines the ways in which these works stand out in the filmography of a director who offers new insights into the notion of cinematic authorship
Appropriate Similarity Measures for Author Cocitation Analysis
We provide a number of new insights into the methodological discussion about author cocitation analysis. We first argue that the use of the Pearson correlation for measuring the similarity between authors’ cocitation profiles is not very satisfactory. We then discuss what kind of similarity measures may be used as an alternative to the Pearson correlation. We consider three similarity measures in particular. One is the well-known cosine. The other two similarity measures have not been used before in the bibliometric literature. Finally, we show by means of an example that our findings have a high practical relevance.information science;Pearson correlation;cosine;similarity measure;author cocitation analysis
Dispelling the Myths Behind First-author Citation Counts
We conducted a full-scale evaluative citation analysis study of scholars in the XML research field to explore just how different from each other author rankings resulting from different citation counting methods actually are, and to demonstrate the capability of emerging data and tools on the Web in supporting more realistic citation counting methods. Our results contest some common arguments for the continued
use of first-author citation counts in the evaluation of scholars, such as high correlations between author rankings by first-author citation counts and other citation
counting methods, and high costs of using more realistic citation counting methods that are not well-supported by the ISI databases. It is argued that increasingly available digital full text research papers make it possible for citation analysis studies to go beyond what the ISI databases have directly supported and to employ more
sophisticated methods
koamabayili/VECTRON-author-checklist: VECTRON author checklist
We have done our best to complete the author checklist relating to the use of animals in the hut study. Note that the objective for the hut study was to evaluate the IRS treatment applications for residual efficacy against Anopheles mosquitoes, including the local An. coluzzii mosquito population. Cows were only used to attract mosquitoes into the huts and no tests were carried out directly on the cows. The author checklist is intended for use with studies where experiments are carried out on animals, which is why we have had such difficulty in completing this for the hut study, as many of the questions do not relate to how the cows were used
Protein expression profiles in Saccharomyces Cerevisiae committed to programmed cell death
Reduced expression of thyroid hormone receptors and beta-adrenergic receptors in human failing cardiomyocytes
An altered thyroid hormone profile has been reported in patients with congestive heart failure. However, information regarding the status of thyroid hormone receptors in human failing cardiomyocytes is lacking. Therefore the expression of thyroid hormone and beta-adrenergic receptors was investigated in human ventricular cardiomyocytes isolated from patients with end-stage heart failure (FM, n=12), or from tentative donors (C, n=4). The expression of thyroid (TRalpha1, and TRbeta1) and beta-adrenergic receptors (ARB1 and ARB2) was measured at both the gene, and at the protein level. In FM the reduced mRNA expression of ARB1 (p<0.05, -37%) and ARB2 (p<0.05, -42%) was associated with a reduction of the messenger for TRalpha1 (p<0.05, -85%) and TRalpha2 (p<0.05, -73%). These findings were confirmed at the protein level for ARB1, ARB2 and TRalpha1. These data reveal that in human heart failure the reduction of beta-adrenergic receptors is associated with reduced expression of both TRalpha1 and TRalpha2 isoforms of thyroid hormone receptors
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