Progress in Cancer Research: Characterisation of a New PPAR β/δ Antagonist, GSK3787, with Roche’s xCELLigence System

PENZBERG, Germany--(BUSINESS WIRE)-- The peroxisome proliferator-activated receptors (PPAR α, β/δ and γ) are nuclear receptors that modulate transcription of regulatory pathways involved in diseases ranging from metabolic syndrome to cancer. They therefore hold great potential as therapeutic targets for the treatment and prevention of disease. PPAR β/δ activation has been reported to increase fatty acid catabolism, ameliorate insulin resistance and decrease serum glucose, implicating a potential significance as a target in the treatment of type 2 diabetes. However, this is clouded by controversial reports on the role of PPAR β/δ in cancer, with some reports suggesting that its activation potentiates tumorigenesis while others suggest that cell proliferation is either unaffected or inhibited by PPAR β/δ activation.

The controversial nature of these reports is largely due to the lack of stringency in approaches used to examine cell proliferation, in particular the limited published time course and concentration-dependent studies. To address this, a recent study used Roche’s (SIX: RO, ROG; OTCQX: RHHBY) xCELLigence system to compare the effects of the PPAR β/δ agonist, GW0742, and the PPAR β/δ antagonist, GSK3787, on proliferation of human cancer cell lines (1). The xCELLigence system allows real-time monitoring of adherent cell proliferation, measuring electrical impedance of cells grown on microsensor arrays integrated into the bottom of each well of a tissue culture E-Plate. A major advantage of this system is that the biological status of cells (including cell number, viability, morphology, and cytoskeletal dynamics) can be measured without the need for addition of chemical labels, which might in turn affect cell physiology. In addition, real-time analysis of cell proliferation provides an outstanding approach over standard techniques, yielding accurate assessment of doubling time during the linear growth phase over a broad concentration range of compound.

The cell lines studied in this system were the human squamous cell carcinoma line A431, human liver cancer cell lines HepG2 and Huh7, human lung cancer cell lines A549 and H1838, and the human breast cancer cell line MCF7. Cells were seeded into the wells of a 16-well E-Plate at a density to obtain optimal exponential growth curves. GW0742 or GSK3787 were added to the cells at concentrations of 0.1, 1.0 or 10 μM. Cell proliferation was monitored every 15min using the xCELLigence system for up to 120h, during the log growth phase.

The results revealed that neither the antagonist GSK3787 nor the agonist GW0742 displayed any toxicity in the six human cancer cell lines studied. In addition activation of PPAR β/δ by the agonist had no influence on cell proliferation. Consistent with this, the antagonist, GSK3787, also had no effect on cell proliferation. These results are observed despite the fact that GW0742 upregulates transcription of known PPARβ/δ target genes (angiopoietin-like protein 4 and adipose differentiation-related protein) both in normal and cancer cells. Although GSK3787 failed to decrease basal expression of these genes, in most cases it antagonised their upregulation induced by GW0742. Achieving such modulatory effects, without promoting cancer cell growth, may be beneficial for the future application of these compounds in vivo.

(1) P.S. Palkar, M.G. Borland, S. Naruhn, C. H. Ferry, C. Lee, U. H. Sk, A. K. Sharma, S. Amin, I. A. Murray, C. R. Anderson, G. H. Perdew, F. J. Gonzalez, R. Müller, and J. M. Peters (2010) Cellular and Pharmacological Selectivity of the PPARβ/δ Antagonist GSK3787, Molecular Pharmacology. doi:10.1124/mol.110.065508.

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 2009, Roche had over 80’000 employees worldwide and invested almost 10 billion Swiss francs in R&D. The Group posted sales of 49.1 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.

For life science research only. Not for use in diagnostic procedures.

XCELLIGENCE is a trademark of Roche.

E-PLATE and ACEA are registered trademarks of ACEA Biosciences, Inc. in the US.

Other brands or product names are trademarks of their respective holders.



CONTACT:

Roche Diagnostics
Dr. Burkhard Ziebolz
Phone: +49 8856 604830
Email: [email protected]

KEYWORDS:   United States  Europe  North America  Switzerland

INDUSTRY KEYWORDS:   Health  Biotechnology  Pharmaceutical

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