An international research team has compiled the first catalogue of tissue-specific pathologies underlying hundreds of inherited diseases.
Researchers compile ‘molecular manual’ for hundreds of inherited diseases
First catalog of tissue-specific changes could improve understanding, help treatment
BOSTON -- An international research team has compiled the first catalogue of tissue-specific pathologies underlying hundreds of inherited diseases. These results provide information that may help treat conditions such as breast cancer, Parkinson’s disease, heart disease and autism. The report from scientists at the Technical University of Denmark and Massachusetts General Hospital (MGH) will appear in the Proceedings of the National Academy of Sciences and has been published online.
"Disease processes in humans are far from being exhaustively understood and characterized, in part because they are the result of complex interactions between many molecules that may take place only in specific tissues or organs. Experiments to directly study these interactions in human patients would not be possible, which limits our understanding of how diseases arise and which molecules and genes are involved," says co-lead author Kasper Lage, PhD, of the MGH Pediatric Surgical Research Laboratories.
Co-lead author Niclas Tue Hansen, MSc, from the Center for Biological Sequence Analysis, Technical University of Denmark, adds, "We let supercomputers model biological processes in tissues across the human organism, based on the knowledge from millions of already published articles. In this way we were able to create an extensive map of the interactions of molecules in many diseases – a sort of molecular manual – without carrying out experiments in patients." The catalogue, which is freely available on the , should help physicians and researchers investigating many serious disorders, he notes.
"It has been extremely exciting to integrate the disease expertise of researchers at MGH and Harvard Medical School with the work of leading systems biologists at the Technical University of Denmark," says Patricia Donahoe, MD, director of Pediatric Surgery Research at MGH and co-corresponding author of the PNAS study. "This current study brought together the strengths of both teams and resulted in a unique way of analyzing inherited diseases. Our findings have the potential to advance the knowledge of pathways, genes and proteins involved in hundreds of human disorders and perhaps contribute to better treatment strategies for some of these serious diseases," Donahoe is the Marshall K. Bartlett Professor of Surgery at Harvard Medical School.
Søren Brunak, PhD, director of the Center for Biological Sequence Analysis at the Technical University of Denmark is co-corresponding author of the PNAS report. Additional authors are Olof Karlberg, PhD, Aron Eklund, PhD, Francisco Roque, MSc, Zoltan Szallasi, MD, and Thomas Skøt Jensen, PhD, all affiliated with the Technical University of Denmark. The study was supported by grants from the Villum Kann Rasmussen Foundation, the Simon Spies Foundation, the National Institute of Child Health and Development, and the National Institutes of Health.
Massachusetts General Hospital, established in 1811, is the original and largest teaching hospital of Harvard Medical School. The MGH conducts the largest hospital-based research program in the United States, with an annual research budget of more than $500 million and major research centers in AIDS, cardiovascular research, cancer, computational and integrative biology, cutaneous biology, human genetics, medical imaging, neurodegenerative disorders, regenerative medicine, systems biology, transplantation biology and photomedicine.
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