Developing and approving new prescription medications can be a costly and time-consuming process. However, findings from this study could partially change that moving forward. According to investigators, instead of developing new medicines, pharmaceutical companies could save time and money by repurposing drugs that have already been approved by the Food and Drug Administration to treat other disorders.
The human genome is composed of genetic instructions, or DNA that is fundamental to health and disease. In order to carry out these instructions, DNA must be read and expressed, and gene expression will be influenced by genetic variation. The same gene may be expressed higher (or lower) in people with certain mutations, which may cause diseases. Scientists analyze collections of gene readouts — or transcriptome — present in cells on hundreds of thousands of individuals. Transcriptome analyses can identify genes differentially expressed between people with and without diseases, and thus lead to a new understanding of the genes associated with certain conditions.
For the new data method, PUMICE (Prediction Using Models Informed by Chromatin conformations and Epigenomics), Penn State researchers integrated transcriptomic, epigenomic and 3D genomic data using a novel machine learning approach. According to the study, PUMICE was successful at identifying drugs that could reverse the expression level of disease genes and may be repurposed to treat several human diseases.
“Traditional approaches that analyze one drug and one disease at a time can be very inefficient,” said Dajiang Liu, co-senior author and associate professor of public health sciences and biochemistry and molecular biology at Penn State. “In contrast, a machine learning approach based on big data, such as PUMICE, can revolutionize biological and clinical research. It will greatly accelerate the process of identifying promising therapeutic targets, and fast forward drug development.”
Using PUMICE, the researchers identified potential treatments for medical conditions, including COVID-19, Alzheimer’s disease and autoimmune diseases, such as Crohn’s disease, rheumatoid arthritis, ulcerative colitis and vitiligo, a skin pigmentation condition. They noted that some of the identified medications are already being evaluated in clinical trials, including Baracitinib, a drug for treating COVID-19.
“Being able to rediscover drugs that are already in clinical trials showcase the power of our approach,” said Bibo Jiang, co-senior author and assistant professor of public health sciences at Penn State. “We will design follow-up experiments to validate new drugs and identify the most promising ones to further test in cell lines and animal models and eventually in clinical trials.”
Chachrit Khunsriraksakul, an MD/PhD student from Penn State College of Medicine led the study. Fellow Penn State researchers Daniel McGuire, Renan Sauteraud, Fang Chen, Lina Yang, Lida Wang, Jordan Hughey, Scott Eckert, J. Dylan Weissenkampen, Ganesh Shenoy, Olivia Marx and Laura Carrel contributed to this research.
The researchers declare no conflicts of interest or specific funding for this research.
Read the full study in Nature Communications.
About Penn State College of Medicine
Located on the campus of Penn State Health Milton S. Hershey Medical Center in Hershey, Pa., Penn State College of Medicine boasts a portfolio of more than $150 million in funded research. Projects range from development of artificial organs and advanced diagnostics to groundbreaking cancer treatments and understanding the fundamental causes of disease. Enrolling its first students in 1967, the College of Medicine has more than 1,700 students and trainees in medicine, nursing, the health professions and biomedical research on its two campuses.