Clinical OMICS

NOV-DEC 2018

Healthcare magazine for research scientists, labs, pathologists, hospitals, cancer centers, physicians and biopharma companies providing news articles, expert interviews and videos about molecular diagnostics in precision medicine

Issue link:

Contents of this Issue


Page 35 of 51

34 Clinical OMICs November/December 2018 A team of researchers from Duke University School Med- ical Center is taking a new approach to developing a treatment for Parkinson's Disease (PD), and it could have implications for developing therapies for other diseases. For the first time, reserachers have successfully modified the expression regulation of the gene that encodes α-synu- clein, SNCA, using an epigenetically based system. Their work provides a proof-of-concept that manipulation of gene expression programs, and more specifically reversing over- expression, by epigenome editing may lead to valuable ther- apeutics for neurological disorders such as PD. The lab of Ornit Chiba-Falek, Ph.D., associate professor in the department of neurology at the Bryan Alzheimer 's Disease Research Center and the Center for Genomic and Computational Biology at Duke University Medical Center studies how dysregulation of gene expression contributes to age related neurodegenerative diseases. Boris Kantor, Ph.D., assistant research professor and director of the Viral Vector Core at Duke develops novel viral vector tools to be used in translational science. The two groups combined their efforts, one on the side of technology and the other focused on the premise, to accomplish this work. They published their results in the August 28th edition of Molecular Therapy in a paper entitled "Downregulation of SNCA expression by targeted editing of DNA-methylation: A potential strategy for precision therapy in PD." Kantor told Clinical OMICs it is incredibly exciting that "an epigenome editing–based system can be applied as a new approach to modify the phenotype of PD, which has no cure." The work is based on the accumulating evidence that ele- vated levels of wild type α-synuclein are causative in the pathogenesis of PD. However, some levels of SNCA are nec- essary to maintain neuronal function which makes a com- plete shutdown of SNCA an unfeasible therapy option and why efforts such as RNAi have come up short. Taking a new approach to an old problem, Chiba-Falek and Kantor sought to develop new therapeutic strategies that intervene with the regulation of SNCA expression, looking to the epigenetic control of gene expression to find their answer. Based on the link between increased SNCA expression and demethylation at SNCA intron 1 and lower methylation levels observed in postmortem samples from PD patients, the team targeted this area to fine tune expres- sion of SNCA. To do this, they developed an all-in-one lentiviral vector, for targeted DNA-methylation editing within intron 1. The By Julianna LeMieux, Ph.D. A 'More Precise' Precision Therapy for Parkinson's Disease Ornit Chiba-Falek, Ph.D., (front) of Duke University Medical Center and her colleague Boris Kantor, Ph.D., are the authors of a paper "Downreg- ulation of SNCA expression by targeted editing of DNA-methylation: A potential strategy for precision therapy in PD" that suggests a potential new approach to developing diagnostics for Parkinson's disease. "Delivery platforms based on lentiviral vectors are highly efficient for CRISPR-dCas9 delivery." —Boris Kantor, Ph.D. Viral Vector Core, Duke University

Articles in this issue

Links on this page

Archives of this issue

view archives of Clinical OMICS - NOV-DEC 2018