Drug Repurposing, Rare Diseases and Semantic Analytics

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Drug Repurposing, Rare Diseases and Semantic Analytics

Rare diseases affect around 6-7% of the population in the developed world (defined as fewer than 1 in 2,000 in Europe and fewer than 200,000 individuals in the US).

By their very definition of serving a relatively small population of people, the cost of developing brand new drugs for this audience (or orphan drugs) can be prohibitively expensive – yet legislation in the U.S. (FDA Orphan Drug Act, 1983), Japan, Australia and Europe incentivises treatment development.

So what’s a pharmaceutical company to do?  Is there a more cost-effective way to reach cures faster?

Enter drug repurposing

On the surface, drug repurposing promises much – known safety profiles of existing drugs, a reduced development timeline and as a result, a significantly reduced cost to market (we’re talking bringing expenditure down from billions of dollars to millions of dollars here).

There’s still a large amount of research to trawl through, a time-consuming and resource-heavy task.  This is why drug companies are currently focusing on automated literature analysis.

Let’s look at the example of Arteriovenous Malformation (AVM), which has been in the news recently in the UK.  It’s a condition which affects hundreds of thousands of people across the world, causing abnormalities in blood vessels.  These abnormalities can result in dangerous complications and disfigurements.  Now, researchers have identified drugs which could target the underlying cause of the condition.

Take a look at this diagram which simplifies the repurposing pipeline from this piece of research:A simplified repurposing pipeline https://www.jci.org/articles/view/98589

Once these genes were identified, the next step in this particular repurposing study was to screen for drugs that targeted the relevant proteins. In this case there were a number of candidate drugs that were already used in cancer therapy.

Here, the disease in question has been taken as the starting point and faulty genes which have been identified on the RAS/MAPK pathway, which controls cell growth.

A simplified repurposing pipeline part 2

In this case, we see that in the treatment of AVM-BRAF mutant zebrafish with the BRAF inhibitor, Vemurafinib, restored blood flow in AVM.

How could semantic analytics play a part?

Drug repurposing relies on making connections, but as mentioned earlier, this is not easy when you’re faced with millions of documents, all with unstructured text.

Semantic annotation 

Wouldn’t it be helpful if a computer could recognise key scientific information in unstructured text, such as scientific papers?  Of course, the answer is yes, but one of the main hurdles with this approach is getting the computer to do this quickly, whilst being able to process scientific synonyms and ambiguity.

Semantic Search

Building on this is semantic search.  A tool which allows a researcher to find relevant information about their target.  In this case, we’re looking for drugs that inhibit BRAF.  As you can see, the search tool also picks up synonyms, ensuring that you don’t miss out on potentially valuable data.  Contrast this with a conventional search engine, where if you search for “drug”, you’ll get results which mention the word “drug”.  However, with a semantically enriched search engine, the computer knows that this actually means anything which is defined as a drug.

Related Reading: Semantic Search vs. Keyword Search

Extracting associations

Picture5

And the results go beyond just highlighting individual entities, allowing you to extract information about relationships between entities, such as gene-phenotype or drug-target.  Extrapolate this over 28 million Medline abstracts, and you have an incredibly powerful tool.

Building a knowledge network

Image: Lopez-Pajares V et al 2013

These relationships can then be built into networks, providing you with a computer readable framework for searching the data and making new connections.

Labelling the entities in the text with unique identifiers allows you to take this a step further and map to other data systems, connecting related diseases, adverse events, pathways, drug labels.

And of course, this method can be turned on its head to discover new information.  For example, you could compare diseases based on their phenotype profiles.  Once you know that two diseases are strongly related, if there’s a drug which treats one of these conditions, you can hypothesise that you have a potential repurposing candidate on your hands for the other condition. This is a technique we’ve explored before here.

Ready to learn more? Listen to SciBite & CCC’s on-demand webinar: Exploring Drug Repurposing for Rare Diseases Through Semantic Analytics

*Editor’s Note: This blog post was originally published on SciBite’s blog on Feb. 28, 2018. 

Michael Hughes

Author: Michael Hughes

A Biologist at heart, Michael has spent his career mining for gold in scientific literature, having worked at the British Oceanographic Centre, Unilever and Thomson Reuters. Prior to his industry experience, he graduated from the University of Sheffield, UK in Zoology, and completed his Masters in Bioinformatics at the University of Liverpool, UK. At SciBite since 2015, he now brings data to life, working with customers on projects and showcasing SciBite’s tools. When he’s not spending time with his young family, Michael likes to go running and hone his photography skills.
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