There are thousands of genes in the human genome that all have different purposes. At least 3,000 of these genes are known to express proteins that can be altered by different medications, however, the FDA has only approved drugs that target around 10 percent of these genes. That means that there are still thousands of genes that have not been thoroughly studied that, with the help of the right medication, could be targeted to help improve human health. The National Institutes of Health Common Fund has awarded 8 U.S. institutions $5.8 million for a new collaborative three-year program called Illuminating the Druggable Genome (IDG) that will study different genes and their potential to be modified by different medicines.
(Image courtesy of Wikimedia)
There are 8 institutions that have been chosen to participate in this collaboration which will all receive the NIH grant:
*Data collected from the NIH RePORTER.
(Image courtesy of Wikmedia)
The IDG program will allow researchers at these 8 institutions to study these genes to see hoe they can be modified by medicines to treat different diseases and disorders. The focus of the program will be on studying genes in the four important druggable families of nuclear receptors, ion channels, protein kinasese, and G-protein coupled receptors (GPRCs).
James M. Anderson, M.D., Ph.D., Director of the NIH Division of Program Coordination, Planning, and Strategic Initiatives, said that “we have a gap in the drug development pipeline between what gene activities we know could be modified by medication and what currently is targeted. By focusing on understudied genes, we hope to find potential targets for medications to treat or cure some of our most burdensome diseases—and then share what we learn so that all can build on this knowledge."
Researchers will explore these so far uncharacterized genes and share their finding with the scientific community so others will be able to use their findings to further both research and clinical translation. With further research into these genes, there is the possibility that new drug targets can be developed that, once they become FDA-approved, will be able to treat more diseases.
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