Cardiotoxicity, which results when drugs adversely affect the heart,
explains why roughly one third of new pharmaceuticals are withdrawn from
the market and why many compounds fail in late-stage clinical testing.
To address this, a research team led by Kyle Kolaja, PhD, in the
Department of Early and Investigative Safety, Nonclinical Safety, at
Roche (SIX:
RO, ROG; OTCQX: RHHBY), in Nutley, New Jersey, USA, reported in the
June issue of Toxicological
Sciences
the identification of a model that more
accurately detects drug-induced cardiac abnormalities. The novelty of
this work is that it integrates two emerging technologies, stem cell
derived tissues and impedance-based real-time cell monitoring.
Using the Roche xCELLigence Cardio Instrument, they discovered that
changes in cell impedance of stem cell derived cardiomyocytes treated
with different compounds were comparable to results from more
established low throughput in vitro technology (e.g.,
measuring electric field potentials via microelectrode arrays).
The xCELLigence Cardio System uses proprietary software and E-Plates 96
to measure electronic cell impedance using sensor electrodes.
Computer-controlled signal generation, automatic frequency scanning, and
a measurement rate of 12.9 milliseconds per 96-well plate, enable
high-speed precise detection of changes in cardiac cell behavior.
Kolaja and his team calculated an index of drug-induced arrhythmias
based on the cytotoxic effects of the drugs tested, enabling the
calculation of a given drug's "predicted proarrhythmic score” (PPS), a
measure of potential cardiotoxicity. According to Kolaja, "We found that
measuring impedance provides a rapid means of interrogating a drug’s
deleterious effect on human cardiac function, and not only helps us in
early discovery safety assessment, but opens up new opportunities for
investigating, cardiac biology, cell signaling and disease pathogenesis.
More importantly, human pluripotent stem cell-based predictive toxicity
assays will help researchers predict potential safety issues of
promising drug candidates early in the development process and provide
insight into the mechanisms of drug-induced organ toxicity.”
The authors of this study raise the possibility that this new model
system may be amenable to high throughput approaches that go beyond hERG
mediated-QT prolongation and delve directly in the functional interplay
of the many ion channels used by human heart muscle to affect normal
function.
About Roche
Headquartered in Basel, Switzerland, Roche is a leader in
research-focused healthcare with combined strengths in pharmaceuticals
and diagnostics. Roche is the world’s largest biotech company with truly
differentiated medicines in oncology, virology, inflammation, metabolism
and CNS. Roche is also the world leader in in-vitro diagnostics,
tissue-based cancer diagnostics and a pioneer in diabetes management.
Roche’s personalised healthcare strategy aims at providing medicines and
diagnostic tools that enable tangible improvements in the health,
quality of life and survival of patients. In 2010, Roche had over 80’000
employees worldwide and invested over 9 billion Swiss francs in R&D. The
Group posted sales of 47.5 billion Swiss francs. Genentech, United
States, is a wholly owned member of the Roche Group. Roche has a
majority stake in Chugai Pharmaceutical, Japan. For more information: www.roche.com.
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