Study identifies novel Parkinsonís disease drug target
Researchers at the MassGeneral Institute for Neurodegenerative Disease (MGH-MIND) have identified a potential new drug target for the treatment of Parkinsonís disease and possibly for other degenerative neurological disorders. In an upcoming issue of the journal Science, the investigators describe finding, in cellular and animal models, that blocking the action of an enzyme called SIRT2 can protect the neurons damaged in Parkinsonís disease from the toxic effects of alpha-synuclein, a protein that accumulates in the brains of Parkinsonís patients. The study, which also suggests that inhibiting this pathway could help in the treatment of other conditions in which abnormal proteins accumulate in the brain, is receiving early online release on the Science Express website.
ďWe have discovered a compelling new therapeutic approach for Parkinsonís disease, which we expect will allow our scientists - as well as those at pharmaceutical and biotech companies - to pursue innovative new drugs that will treat and perhaps even cure this disorder,Ē says Aleksey Kazantsev, PhD, director of MGH-MIND Drug Discovery Laboratory, who led the Science study. ďSince the same sort of aggregation of misfolded proteins has been reported in Huntingtonís and Alzheimerís diseases - as well as Lewy body dementia, which also involves alpha-synuclein deposits - we plan to test this approach in those conditions as well.Ē
Parkinsonís disease - characterized by tremors, rigidity, difficulty walking and other symptoms - is caused by the destruction of brain cells that produce the neurotransmitter dopamine. In recent years researchers at several centers have been studying the role of alpha-synuclein accumulations in dopamine-producing neurons, observed in patients with both inherited and sporadic Parkinsonís disease. MGH-MIND investigators have discovered that, in Parkinsonís, the alpha-synuclein molecule folds abnormally and form aggregates called inclusion bodies. Such inclusions of other abnormal proteins are seen in several disorders, but whether inclusions are toxic or protective to neurons has been controversial.
In a paper published last year in the Proceedings of the National Academy of Sciences, a research team led by Kazantsev analyzed ways to reduce the size of inclusions containing misfolded versions of alpha-synuclein or of the Huntingtonís disease-associated protein huntingtin. They found that a compound called B2, which promotes the formation of larger inclusions, paradoxically appeared to reduce toxicity in cellular disease models, possibly by reducing the overall number of inclusions.
In the current study, the investigators began by seeking the mechanism underlying the observed effects of B2. Assays of the compoundís activity against a panel of key enzymes identified only one significant association - a weak but selective inhibition of SIRT2, which is known to regulate the cell cycle and may have a role in aging. An experiment using RNA interference to suppress SIRT2 and a related enzyme in human cell lines expressing alpha-synuclein confirmed that only the inhibition of SIRT2 reduced alpha-synuclein toxicity.
Kazantsevís team then developed and identified more powerful inhibitors of SIRT2, based on the structure of B2. One of these novel inhibitors called AGK2 had 10 times the potency of B2 and was shown to protect dopamine-producing neurons from alpha-synuclein toxicity in cultured rat neurons and in an insect model of PD. Several additional compounds that act on the SIRT2 pathway have been identified, some which may be even better than AGK2 as candidates for drug development.
SIRT2 is known to act on a major protein component of microtubules, cellular structures that help move objects within cells, among other functions. The researchers theorize that inhibiting SIRT2 might promote microtubule-dependent transportation of alpha-synuclein into large aggregates; or it could strengthen microtubules that have been destabilized by misfolded alpha-synuclein.
Kazantsev explains, ďFor Parkinsonís disease, we can now pursue a straightforward drug development process by identifying potent and selective candidates from this class of compounds that can be tested in animal studies and eventual human trials. One of the most satisfying aspects is how this discovery validates our approach to drug discovery, which incorporates both the most advanced tools for screening candidate compounds and outstanding collaboration with our clinical and scientific experts in human disease.Ē Kazantsev is an assistant professor of Neurology at Harvard Medical School.
Co-authors of the Science report are first author Tiago Outeiro, PhD, and co-authors Steve Altman, Allison Amore, Michele Maxwell, PhD, Pamela McLean, PhD, Anne Young, MD, PhD, and Bradley Hyman, MD, PhD, of MGH-MIND; Eirene Kontopoulos and Mel Feany, MD, PhD, Brigham and Womenís Hospital; Irina Kufareva, PhD, and Ruben Abagyan, PhD, Scripps Research Institute; and Katherine Strathearn, Catherine Volk, and Jean-Christophe Rochet, PhD, Purdue University. The study was supported by private donations to MGH-MIND and grants from the National Institutes of Health and the Massachusetts Biomedical Research Corporation.
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. MGH and Brigham and Womenís Hospital are founding members of Partners HealthCare HealthCare System, a Boston-based integrated health care delivery system.
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