4.3 Article

mTOR, a Potential Target to Treat Autism Spectrum Disorder

Journal

CNS & NEUROLOGICAL DISORDERS-DRUG TARGETS
Volume 15, Issue 5, Pages 533-543

Publisher

BENTHAM SCIENCE PUBL
DOI: 10.2174/1871527315666160413120638

Keywords

Autophagy; fragile X syndrome; mammalian target of rapamycin; metabotropic glutamate receptor 5; neurofibromatosis; phosphatase and tensin homolog; tuberous sclerosis complex

Funding

  1. Ministry of Education, Culture, Sports, Science and Technology (MEXT) KAKENHI [26860836]
  2. Practical Research Project for Rare/Intractable Diseases Program from Japan Agency for Medical Research and Development [H27-Itaku(Nan)-Ippan-015]

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Mammalian target of rapamycin (mTOR) is a key regulator in various cellular processes, including cell growth, gene expression, and synaptic functions. Autism spectrum disorder (ASD) is frequently accompanied by monogenic disorders, such as tuberous sclerosis complex, phosphatase and tensin homolog tumor hamartoma syndrome, neurofibromatosis 1, and fragile X syndrome, in which mTOR is hyperactive. Mutations in the genes involved in the mTOR-mediated signaling pathway have been identified in some cases of syndromic ASD. Evidences indicate a pathogenic role for hyperactive mTOR-mediated signaling in ASD associated with these monogenic disorders, and mTOR inhibitors are a potential pharmacotherapy for ASD. Abnormal synaptic transmission through metabotropic glutamate receptor 5 may underlie in a part of ASD associated with hyperactive mTOR-mediated signaling. In this review, the relationship between mTOR and ASD is discussed.

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