Largest census of cancer genes to help understand drug targets
Cancer Gene Census paves the way for improvements in personalised medicine
Researchers at the Wellcome Sanger Institute have created the first comprehensive summary of all genes known to be involved in human cancer, the “Cancer Gene Census”. Describing all genes strongly implicated in causing cancer, the Census also describes how they function across all forms of this disease. Reported in Nature Reviews Cancer, the resource catalogues over 700 genes, to help scientists understand the causes of cancers, find drug targets and design treatments.
The study characterises the increasing understanding that many genes have multiple different roles in different cancers. This paves the way for improvements in personalised medicine, and building combinations of anti-cancer drugs for any given set of genetic functions or mutations.
To address this, researchers working with the Catalogue of Somatic Mutations in Cancer (COSMIC) have created the Cancer Gene Census. While the COSMIC database characterises over 1,500 different forms of human cancer and types of mutations, the Cancer Gene Census describes which genes are fundamentally involved and describes how these genes cause disease.
For the first time ever, functional changes to these genes are summarised in terms of the ten Cancer Hallmarks – biological processes that drive cancer. Mutations in some genes lead to errors in repairing DNA, whereas mutations in other genes can suppress the immune system or promote tumour invasion or spreading. Across the 700 genes in the Cancer Gene Census, many have two or more different ways of causing cancer. These are often different and sometimes contradictory depending on the tumour type, and are all described in this single resource.
The scientists have manually condensed almost two thousand papers to draw together strong evidence of a gene’s role in cancer, and describe which genetic functions go wrong to cause cancer. This knowledge is crucial to developing new therapeutics. When combined with the COSMIC database, it is now possible to characterise exactly which cancers are impacted by which genes, and which mutations are likely involved.
Cancer is a genetic disease, and mutations in DNA can affect cells so that they are able to grow uncontrollably. Cancer can form in over 200 parts of the body and hundreds of different genes are known to be involved. To understand individual cancers and design specific treatments, many complex details need to be combined. However, this information is often spread out across thousands of different scientific publications and public databases.
“Scientific literature is very compartmentalised. With the Cancer Gene Census, we’re breaking down all those compartments and putting everything together to reveal the full complexity of cancer genetics. This is the broadest and most detailed review of human cancer genes and their functions ever created and will be continually updated and expanded to keep it at the forefront of cancer genetics research.”
Dr Zbyslaw Sondka The lead author on the project from the Wellcome Sanger Institute
“The combination of the Cancer Gene Census with COSMIC will enable researchers to investigate individual mutations and try to find good targets for anti-cancer drugs based on the actual processes involved. It will also allow biologists and pharmaceutical scientists to see patterns and target particular pathways with anti-cancer drugs, not solely single genes. We hope that this resource will help to make precision medicine even more precise.”
Simon Forbes Senior author on the paper who heads COSMIC, at the Wellcome Sanger Institute
Some genes have a particular function in one type of cancer cell, but a completely different and opposite mode of action in another cancer. This affects what drugs would be effective against each individual cancer. By bringing all the information together, the Cancer Gene Census makes it easier for researchers to see all the different functions of each gene and target only the desired effect. This could also help delay drug resistance.
“One of the biggest problems in treating cancer is the emergence of drug resistance. By showing the similarities of functions across different genes, the Cancer Gene Census could help reveal which combinations of drugs could be effective in any particular cancer, and possibly prevent some cases of resistance. This is a fabulous resource and could underpin precision oncology development.”
Dr Ian Dunham An author on the paper from Open Targets, a public-private partnership that uses genetics and genomics data for systematic drug target identification and prioritisation
Zbyslaw Sondka et al. (2018) The COSMIC Cancer Gene Census: describing genetic dysfunction across all human cancers. Nature Reviews Cancer. DOI: 10.1038/ s41568-018-0060-1
This study was supported by Wellcome and the Open Targets program OTAR007.
COSMIC – the Catalogue of Somatic Mutations in Cancer
A key resource underpinning cancer genetic research, COSMIC provides large high-quality datasets, methods and graphics to scrutinise the genetics causing this disease, giving insights to pharmaceutical design and patient therapies. Built within the world-leading Wellcome Trust Sanger Institute (UK) to support global research, millions of mutations across thousands of diseases can be explored at http://cancer.sanger.ac.uk
Open Targets covers all aspects of human health and disease. The cornerstone of the collaboration is an agreement that experimental data and information gathered within the initiative will be shared openly, to benefit the broader scientific community. Open Targets welcomes new interest from companies and academic institutions that wish to accelerate the discovery of drug targets through open innovation.
The Wellcome Sanger Institute
The Wellcome Sanger Institute is one of the world's leading genome centres. Through its ability to conduct research at scale, it is able to engage in bold and long-term exploratory projects that are designed to influence and empower medical science globally. Institute research findings, generated through its own research programmes and through its leading role in international consortia, are being used to develop new diagnostics and treatments for human disease. To celebrate its 25th year in 2018, the Institute is sequencing 25 new genomes of species in the UK. Find out more at www.sanger.ac.uk or follow @sangerinstitute
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