Sensitive technique makes it possible to study the delivery of RNA drugs

In recent years, RNA molecules, with the ability to affect or turn off pathogenic genes, have become promising drug candidates in several areas. However, it has been a challenge to develop techniques to deliver the RNA molecules into the cells where they have an effect. Researchers at Lund University in Sweden have now developed a sensitive technique that makes it possible to study the delivery into the cell, and have shown a possible way to effectively deliver RNA drugs to tumors. The study has now been published in Nature Communications.

DNA and its chemical relative, RNA, are molecules that all living organisms use for storing information and carrying out different functions in the cell. In the study in question, the researchers have studied a type of RNA drug called siRNA. During the 1990s, researchers discovered that siRNA, small double-stranded RNA molecules, could be used to turn off virtually any gene. The phenomenon was named RNA interference. In 2006, the discovery was awarded the Nobel Prize in Physiology or Medicine. There were considerable hopes that RNA interference could be used in the treatment of virus infections, cancer and other diseases.

"Two siRNA drugs have been approved by the FDA, but as yet, no drug has been approved for clinical use in cancer", says cancer researcher and physician Anders Wittrup at Lund University and Skåne University Hospital who led the study.

One considerable advantage of using RNA molecules is that they can be rapidly developed and produced. The major problem for all sorts of RNA drugs is getting these molecules into the interior of the cell, the so-called cytosol, where they have an effect. The size of the SiRNA molecule - about 50 times larger than a typical drug molecule - is a factor. In the study in question, the researchers studied siRNA molecules linked with cholesterol, which means that they are taken up effectively by most tumor cells.

Even if we can make tumor cells take up siRNA, it has been observed that 99 per cent appears to get caught in a type of cellular waste dump, the so-called lysosome."

Anders Wittrup, cancer researcher and physician, Lund University

The researchers then examined if, among other things, the use of the malaria drug chloroquine could cause damage in the lysosome, so that the siRNA drug could enter further into the cell. Being able to study this required new imaging techniques in order to see what happens in the cell.

"The completely new microscopy methods make it possible to study in detail when lysosomes and other structures in the cell are opened up for RNA delivery. This is a technique that is in high demand in both academic research and within the pharmaceutical industry", says doctoral student Hampus Du Rietz.

"We have shown how chloroquine can be used so that the siRNA molecules enter the cytosol, i.e. the space between the cell membrane and the nucleus of the cell", says Anders Wittrup.

This way of opening the lysosomes, which previously encapsulated the RNA molecules and thus prevented their effect, means that the main obstacle for the use of siRNA and other RNA-based drugs is now potentially on the way to being removed.

"We see a siRNA effect that is 50 times higher in cell culture studies and also effective delivery in the experimental tumors cultivated outside the body, so-called tumor spheroids, that could not previously be reached by siRNA", says Anders Wittrup.

More studies are needed before RNA drugs are put in clinical use. The research team in Lund has now gone on to studies of more tumor types and other methods of delivering RNA into tumor cells.

"Our findings open up exciting possibilities for how RNA can reach into the interior of cells. I think it will play a crucial role in developing RNA drugs for the treatment of diseases for which we currently lack effective drugs", concludes Anders Wittrup.

Journal reference:

Du Rietz, H., et al. (2020) Imaging small molecule-induced endosomal escape of siRNA. Nature Communications.


The opinions expressed here are the views of the writer and do not necessarily reflect the views and opinions of AZoLifeSciences.
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