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Pharmacological prospects of G-quadruplexes for neurological diseases using porphyrins.
Asamitsu, Sefan; Yabuki, Yasushi; Ikenoshita, Susumu; Wada, Takahito; Shioda, Norifumi.
Affiliation
  • Asamitsu S; Department of Genomic Neurology, Institute of Molecular Embryology and Genetics (IMEG), Kumamoto University, 2-2-1 Honjo, Chuo-ku, Kumamoto, 860-0811, Japan.
  • Yabuki Y; Department of Genomic Neurology, Institute of Molecular Embryology and Genetics (IMEG), Kumamoto University, 2-2-1 Honjo, Chuo-ku, Kumamoto, 860-0811, Japan.
  • Ikenoshita S; Department of Genomic Neurology, Institute of Molecular Embryology and Genetics (IMEG), Kumamoto University, 2-2-1 Honjo, Chuo-ku, Kumamoto, 860-0811, Japan; Department of Neurology, Graduate School of Medical Sciences, Kumamoto University, 1-1-1 Honjo, Chuo-ku, Kumamoto, 860-8556, Japan.
  • Wada T; Department of Medical Ethics and Medical Genetics, Kyoto University Graduate School of Medicine, Yoshida-Konoe-cho, Sakyo-ku, Kyoto, 606-8501, Japan.
  • Shioda N; Department of Genomic Neurology, Institute of Molecular Embryology and Genetics (IMEG), Kumamoto University, 2-2-1 Honjo, Chuo-ku, Kumamoto, 860-0811, Japan. Electronic address: shioda@kumamoto-u.ac.jp.
Biochem Biophys Res Commun ; 531(1): 51-55, 2020 10 08.
Article in En | MEDLINE | ID: mdl-31980177
Genomic regions with guanine (G)-rich sequences make non-Watson-Crick base pairs, which result in the formation of unique nucleic acid structures called G-quadruplexes (G4s) in cells. Studies have suggested that abnormal G4s are involved in neurological diseases. For example, the formation of G4s caused by expansion of G-rich sequences is implicated in C9orf72-mediated amyotrophic lateral sclerosis and frontotemporal dementia (C9ALS/FTD), and fragile X-related tremor/ataxia syndrome (FXTAS). In addition, the disruption and/or mutation of G4 binding proteins (G4BPs), such as heterogeneous nuclear ribonucleoproteins (hnRNPs) and DNA/RNA helicases, is related to neurological diseases. For instance, mutations in a G4BP called ATRX lead to a neurodevelopmental disorder, ATR-X syndrome, which is associated with intellectual disability. We found that porphyrins are potential candidate drugs for treating ATR-X syndrome through their G4 binding ability. Importantly, intracellular porphyrins are produced from 5-aminolevulinic acid (5-ALA) in vivo. Oral administration of 5-ALA improved cognitive dysfunction in an ATR-X syndrome model mouse, and language ability in an ATR-X syndrome patient. In this review, we suggest a novel therapeutic strategy targeting G4s using porphyrins in neurological diseases.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Porphyrins / Alpha-Thalassemia / Mental Retardation, X-Linked / G-Quadruplexes Limits: Animals / Humans Language: En Journal: Biochem Biophys Res Commun Year: 2020 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Porphyrins / Alpha-Thalassemia / Mental Retardation, X-Linked / G-Quadruplexes Limits: Animals / Humans Language: En Journal: Biochem Biophys Res Commun Year: 2020 Document type: Article Affiliation country: Country of publication: