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Drug development speeds up with more advanced microarray technology

Date:
April 21, 2011
Source:
Technical Research Centre of Finland (VTT)
Summary:
RNA interference technology, which is used in cell biology, has revolutionized functional research of the gene products in the last ten years. Now researchers have developed a method which allows a single microchip to be used to screen the functions of tens of thousands of genes simultaneously by means of RNA interference. Traditional methods only allow a few hundred genes to be screened with each microplate.

RNA interference technology, which is used in cell biology, has revolutionised functional research of the gene products in the last ten years. VTT Technical Research Centre of Finland has developed a method which allows a single microchip to be used to screen the functions of tens of thousands of genes simultaneously by means of RNA interference. Traditional methods only allow a few hundred genes to be screened with each microplate, and therefore the new method will accelerate VTT's service offering in the field of drug development.

"VTT has already tested the method on a panel of almost one hundred cancer cell types and found it to be both efficient and reliable. We have used the method especially in breast cancer and prostate cancer studies," explains Juha Rantala, a research scientist at VTT and the founder of the method.

The primary benefit of the method is that it allows such a large number of samples to be analysed simultaneously, which saves both money and human resources, and speeds up research considerably. The findings of the study were published in March 2011 in BMC Genomics, a journal specialising in the methodologies of genetic research.

Miniaturised cell spot microarray techniques, which are used to analyse the functioning of cells, have featured in drug development at VTT for a few years now, and they are both an important research tool and a development priority. Ultra-high throughput screening (UHTS) techniques are used at VTT to study how one gene or groups of genes regulate the cell activities, and how the cell functions promote health, or cause illnesses. RNA interference technology allows genes to be "silenced" and thereby inhibit protein production of genes. Potential future use of RNAi technology includes also the diagnosis and treatment of illnesses.

The unique method developed by VTT is mostly used in genomic-scale analyses which have previously been very expensive. The new technology is believed to give VTT a competitive advantage in genome research which is of special interest of the drug industry. Other potential applications include studying the combined effects of genes and drugs. Research scientists at VTT have also cited the method previously in a scientific publication focusing on the cell division of breast cancer cells. The method is believed to significantly boost VTT's commercial activities with the drug industry.


Story Source:

The above story is based on materials provided by Technical Research Centre of Finland (VTT). Note: Materials may be edited for content and length.


Journal Reference:

  1. Juha K Rantala, Rami Mไkelไ, Anna-Riina Aaltola, Petra Laasola, John-Patrick Mpindi, Matthias Nees, Petri Saviranta, Olli Kallioniemi. A cell spot microarray method for production of high density siRNA transfection microarrays. BMC Genomics, 2011; 12 (1): 162 DOI: 10.1186/1471-2164-12-162

Cite This Page:

Technical Research Centre of Finland (VTT). "Drug development speeds up with more advanced microarray technology." ScienceDaily. ScienceDaily, 21 April 2011. <www.sciencedaily.com/releases/2011/04/110420081813.htm>.
Technical Research Centre of Finland (VTT). (2011, April 21). Drug development speeds up with more advanced microarray technology. ScienceDaily. Retrieved July 22, 2014 from www.sciencedaily.com/releases/2011/04/110420081813.htm
Technical Research Centre of Finland (VTT). "Drug development speeds up with more advanced microarray technology." ScienceDaily. www.sciencedaily.com/releases/2011/04/110420081813.htm (accessed July 22, 2014).

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