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Bayer AG: New Stakes in Stem Cells

Prof. Andreas Busch, Member of the Bayer HealthCare Executive Committee, responsible for Global Drug Discovery

Prof. Andreas BuschJanuary 2011. An unmasked account of decisions about investing into cancer stem cell research and the fate of regenerative medicine projects in Japan. Dr Busch summarises results and evaluates technology platforms like novel antibodies and wnt mechanisms. He voices his expectations from current key drug development partnerships, in particular with Oncomed and Micromet. Will these include companion diagnostics? To what extent does Bayer retain respective intellectual property rights? A comment on personalised medicine and cancer stem cells research pursued by Merck KGaA and others. What are prospects for classic oncology drugs?

 

 

 

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Drug Testing with Embryonic Stem Cells

– Towards Standards For Assays

(C) David C Hay 2009As stem cell derived models of human liver biology move closer to diagnostic implementation there is an imperative for model standardization. Fresh experimental data is provided.

 

 

 

 

 

Reference
Hay DC (2009): Drug Testing with Embryonic Stem Cells – Towards Standards For Assays. published online September 12, B2Bioworld.com.



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Methods, reviewed, 3 pages

Stem Cell Insights Collection 2010

Issues and Evaluation from Pharma Leaders

How does the pharma industry view application of stem cell technologies? Where are R&D efforts needed, and where does academic research not fulfill expectations? What is the role of suppliers in the field?

Read fresh answers from the leaders, provided exclusively to readers of B2Bioworld. Published only here, and all in one.

 

(C) Boehringer Ingelheim(C) Wolf G Kroner 2009(C) Wolf G Kroner 2009(C) Hoffmann-La Roche 2009

 

We are obliged to more and more move away from animal models
- Prof. Andreas Barner, Boehringer Ingelheim


Preparing for Another Level of Innovation
- Dr Mark Fishman, Novartis


Clear away complete confusion of terms
- Dr Bernhard Kirschbaum, Merck Serono


Stem Cells: a discovery tool and a potential therapeutic modality
- Dr Jonathan Knowles, Hoffmann-La Roche

 

(C) R.McKernan 2009(C) Wolf G Kroner 2009(C) M. Krogsgaard(C) K. Stoeckli

 

It really started last year…
- Dr Ruth McKernan, Pfizer Regenerative Medicine


Stem Cells and Vaccines Production
- Dr Majid Mehtali, Vivalis


Doing our business a little bit differently than the others in the industry
- Dr Mads Krogsgaard, Novo Nordisk


Triggering Regenerative Functions with Transplanted Cells and Small Molecules
- Dr Kurt Stoeckli, Biological Sciences/Discovery Sanofi-Aventis

 

(C) P. Vallance(C) Hugh Ilyine 2009(C) S. Tegethoff 2009(C) D. Hay 2009


Stem Cell Research in GlaxoSmithKline and Beyond
- Dr Patrick Vallance, GlaxoSmithKline Drug Discovery


Stem Cells – Failings and Deliveries
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Patenting Stem Cells
- Dr. Sebastian Tegethoff, 24IP


Drug Testing with Embryonic Stem Cells – Towards Standards For Assays
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L’Oréal avance dans les cellules souches
- Report by Hélène Guyot (with summary in English)


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Related Article 

Bayer AG: New Stakes in Stem Cells
- Prof. Andreas Busch, Bayer AG



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Pfizer Regenerative Medicine: “It really started last year…”

Ruth McKernan (c) Pfizer Inc.Pfizer is rapidly expanding work on stem cell applications. A first hand account by Dr Ruth McKernan, the global CSO of Pfizer’s activities in the field, an evaluation of toxicity screening with embryonic stem cells and needs to move forward.

 

 

 

 

 



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exclusive interview, 3 pages

xCELLigence System for Cell Analysis

xCelligence RTCA DPThe extent to which protein targets are modulated by drugs or small molecule compounds depends on a number of factors, including the expression levels of the target, the effective concentration of the compound, and the time needed for the compound to perturb the target. One of the limitations of current multidimensional phenotypic profiling approaches is that typically a single time point is chosen to assess the effect of compounds. The conclusion, regarding the compounds´ mechanism of action, is based on the time point at which the samples are processed.

To address these restrictions, researchers Abassi et al. (1) have devised a live cell morphological profiling approach for dynamic monitoring of the effect of small molecule compounds that was based on impedance measurement of cells with the xCELLigence RTCA System of Roche Applied Science (SIX: RO, ROG; OTCQX: RHHBY). The approach was tested by screening a library containing FDA approved drugs, experimental compounds, and natural compounds. Compounds with similar activity produced similar impedance-based Time-dependent Cell Response Profiles (TCRPs). The compounds were clustered then based on TCRP similarity.

The researchers identified novel mechanisms for existing drugs, confirmed previously reported calcium modulating activity for COX-2 inhibitor celecoxib, and discovered an additional mechanism for the experimental compound monastrol. They also recognized and characterized a new antimitotic agent. This approach will also help to detect the off target effect of a given compound.

The TCRP technique described by Abassi et al. can overcome the limitations of current approaches, because the profile generated is time dependent. In combination with measurement of cell number, morphology, and adhesion, the TCR technique allows greater expansion of the ‘‘biological space’’ at which compounds are screened. It provides ample opportunity to detect and identify biological activity associated with small molecules.

In conclusion, these findings indicate that the time-dependant resolution, provided by the TCRP approach, can be used in conjunction with phenotypic profiling approaches to obtain additional data associated with small molecule compounds. TCRP approach provides predictive mechanistic information for small molecule compounds.

The non-invasive and label-free xCELLigence analysis method, originally invented by ACEA Biosciences in San Diego, USA is based on measuring the impedance of cells. The technique utilizes an electronic readout of impedance to non-invasively quantify cellular status in real-time. Cells are seeded in E-Plate microtiter plates, which are integrated with microelectronic sensor arrays. The interaction of cells with the microelectrode surface generates a cell-electrode impedance response, which not only indicates cell viability but also correlates with the number of the cells seeded in the well. In conjunction with its user-friendly data collection and analysis capabilities, the xCELLigence System makes a unique platform for continuous, real-time cell-based assays and provides a huge opportunity for cellular and molecular biology.

 

For more information on the technology, please visit www.roche-applied-science.com.

Literature:

(1) Abassi YA et al.: Kinetic cell-based morphological screening: prediction of mechanism of compound action and off-target effects. Chem Biol 2009; 16:712-723.

 

More information: www.xCELLigence.roche.com.

All trademarks used or mentioned in this release are protected by law.XCELLIGENCE is a trademark of Roche.E-PLATE and ACEA BIOSCIENCES are registered trademarks of ACEA Biosciences, Inc. in the US.

 

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