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Microsoft word - case_study_drug_combinations.doc


Exploring the molecular basis of combination
drugs using ToxWiz

For further information:
Email: info@camcellnet.com
Tel: +44 1223 703 137 Fax: +44 1223 858 794
Drug combinations represent intriguing possibilities for new therapies. The
basic principle is that two active compounds can lead to effects that are more
than the sum of their parts, possibly by simultaneously blocking two parts of
the same pathway, or by one compound augmenting the activity of another.
Borisy et al (2003), from CombinatoRx systematically screened about 120 000
combinations of reference listed drugs to find combinations that had new
activities. We investigated the handful of combinations for which new
activities were found, to see if we could, using our database and software,
suggest how one drug could complement another.
One of the interesting combination effects they reported was that the
antiplatelet drug dipyridamole, when combined with the glucocorticoid
dexamethasone, prevented TNF-α production in response to stimulation by
phorbol 12-myristate 13-acetate (PMA) or ionomycin. We sought the best
possible paths between these two drugs using ToxWiz and also explored
additional connections between them by exploring the interaction network
around these two compounds (see Figure 1).
Figure 1 Some of the possible biological links between dexamethasone and
dipyridamole suggested by ToxWiz. The targets for the two drugs are boxed in
red. TNF-alpha is boxed in blue.
There are several possibilites for how these two drugs can affect each other
inside the system. As pointed out by Borisy et al (2003), the effects of
steroids, like dexamethasone, on TNF are wel documented (Joyce et al,
1997), and anti-TNF effects of dipyridamole are thought to be due to its
blockage of adenosine uptake. However, their combined mode of action could
not be explained by these prior observations (Borisy et al, 2003).
Interrogation of CCNet’s vast database of protein-protein and protein-
chemical associations, however, suggested other possibilities (Figure 1). One
particularly interesting possibility arises owing to a screening result, where
dipyridamole was one of 220 compounds found to inhibit HSP90 in tumor cell
lysate (Rodina et al, 2007). The relationship between HSP90 like molecules,
such as TRAP-1, and TNF is well understood – complexes involving HSP90
are often critical for TNF mediated signaling (e.g. Chen et al, 2002). It is
compelling to suggest that affects of TNF signaling could be due to the
inhibition of HSP90, thus operating in a manner similar to the well known
HSP90 inhibitor geldenamycin, which itself can decrease TNF secretion in
response to inflammatory stimulants (Vega et al, 2003).
There are several other possibilities for interactions between these two drugs
suggested by the system. These possible relationships became apparent after
just a few minutes of study, thus demonstrating the power of the very fast
synthesis of data from diverse sources to arrive at hypotheses very quickly.
References
Borisy AA, Elliott PJ, Hurst NW, Lee MS, Lehar J, Price ER, Serbedzija G, Zimmermann GR,
Foley MA, Stockwel BR, Keith CT. Systematic discovery of multicomponent therapeutics.
Proc Natl Acad Sci USA. 2003 Jun 24;100(13):7977-82.
Chen G, Cao P, Goeddel DV. TNF-induced recruitment and activation of the IKK complex
require Cdc37 and Hsp90. Mol Cell. 2002 Feb;9(2):401-10.
Joyce DA, Steer JH, Abraham LJ. Glucocorticoid modulation of human
monocyte/macrophage function: control of TNF-alpha secretion. Inflamm Res. 1997
Nov;46(11):447-51.
Rodina A, Vilenchik M, Moulick K, Aguirre J, Kim J, Chiang A, Litz J, Clement CC, Kang Y,
She Y, Wu N, Felts S, Wipf P, Massague J, Jiang X, Brodsky JL, Krystal GW, Chiosis G.
Selective compounds define Hsp90 as a major inhibitor of apoptosis in small-cell lung cancer.
Nat Chem Biol. 2007 Aug;3(8):498-507.
Vega VL, De Maio A. Geldanamycin treatment ameliorates the response to LPS in murine
macrophages by decreasing CD14 surface expression. Mol Biol Cell. 2003 Feb;14(2):764-73.
About Cambridge Cell Networks
Cambridge Cell Networks (CCNet) based in Cambridge, UK supplies a range of industry-
leading content on biological pathways, chemistry and toxicology, combined with an
integrated pathway visualisation and exploration tools to the pharmaceutical and
biotechnology industries. Using cutting-edge biological and computational methods combined
with knowledge management techniques, CCNet offers a novel approach to pathway
analysis, providing effective target validation and predictive toxicology data, which will ensure
the production of safer drugs.
The Company was founded in 2002 by eminent scientific figures from the European
Bioinformatics Institute in Cambridge, UK, the University of Cambridge and the European
Molecular Biology Laboratory in Heidelberg, Germany. CCNet has facilities in three countries
and is staffed by a team of expert biochemists, pharmacologists, bioinformaticians, chemists
and industrial toxicologists.

Source: http://www.camcellnet.com/case_studies/camcellnet_drug_comb_cs1.pdf

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