Literature DB >> 22387408

Is seladin-1 really a selective Alzheimer's disease indicator?

Laura J Sharpe1, Jenny Wong, Brett Garner, Glenda M Halliday, Andrew J Brown.   

Abstract

Selective Alzheimer's Disease Indicator-1 (Seladin-1) was originally identified by its down-regulation in the brains of Alzheimer's disease (AD) patients. Here, we re-examine existing data and present new gene expression data that refutes its role as a selective AD indicator. Furthermore, we caution against the use of the name "Seladin-1" and instead recommend adoption of the approved nomenclature, 3β-hydroxysterol Δ24-reductase (or DHCR24), which describes its catalytic function in cholesterol synthesis. Further work is required to determine what link, if any, exists between DHCR24 and AD.

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Year:  2012        PMID: 22387408     DOI: 10.3233/JAD-2012-111955

Source DB:  PubMed          Journal:  J Alzheimers Dis        ISSN: 1387-2877            Impact factor:   4.472


  12 in total

1.  The terminal enzymes of cholesterol synthesis, DHCR24 and DHCR7, interact physically and functionally.

Authors:  Winnie Luu; Gene Hart-Smith; Laura J Sharpe; Andrew J Brown
Journal:  J Lipid Res       Date:  2015-01-31       Impact factor: 5.922

2.  Signaling regulates activity of DHCR24, the final enzyme in cholesterol synthesis.

Authors:  Winnie Luu; Eser J Zerenturk; Ika Kristiana; Martin P Bucknall; Laura J Sharpe; Andrew J Brown
Journal:  J Lipid Res       Date:  2013-12-20       Impact factor: 5.922

3.  Alzheimer's disease: brain desmosterol levels.

Authors:  Thomas Wisniewski; Kia Newman; Norman B Javitt
Journal:  J Alzheimers Dis       Date:  2013       Impact factor: 4.472

4.  Altered expression of 3-betahydroxysterol delta-24-reductase/selective Alzheimer's disease indicator-1 gene in Huntington's disease models.

Authors:  Athina Samara; Mariarita Galbiati; Paola Luciani; Cristiana Deledda; Elio Messi; Alessandro Peri; Roberto Maggi
Journal:  J Endocrinol Invest       Date:  2014-06-11       Impact factor: 4.256

5.  Subcellular localization of sterol biosynthesis enzymes.

Authors:  Katalin Koczok; Channabasavaiah B Gurumurthy; István Balogh; Zeljka Korade; Károly Mirnics
Journal:  J Mol Histol       Date:  2018-12-08       Impact factor: 3.156

Review 6.  Liver X receptors and cholesterol metabolism: role in ventral midbrain development and neurodegeneration.

Authors:  Spyridon Theofilopoulos; Ernest Arenas
Journal:  F1000Prime Rep       Date:  2015-04-02

7.  3 β-hydroxysteroid-Δ 24 reductase (DHCR24) protects neuronal cells from apoptotic cell death induced by endoplasmic reticulum (ER) stress.

Authors:  Xiuli Lu; Yang Li; Weiqi Wang; Shuchao Chen; Ting Liu; Dan Jia; Xiaoping Quan; Deliang Sun; Alan K Chang; Bing Gao
Journal:  PLoS One       Date:  2014-01-29       Impact factor: 3.240

8.  Expression and function of Abcg4 in the mouse blood-brain barrier: role in restricting the brain entry of amyloid-β peptide.

Authors:  Agnès Dodacki; Matthew Wortman; Bruno Saubaméa; Stéphanie Chasseigneaux; Sophie Nicolic; Nathalie Prince; Murielle Lochus; Anne-Laure Raveu; Xavier Declèves; Jean-Michel Scherrmann; Shailendra B Patel; Fanchon Bourasset
Journal:  Sci Rep       Date:  2017-10-17       Impact factor: 4.379

Review 9.  Regulation of Brain Cholesterol: What Role Do Liver X Receptors Play in Neurodegenerative Diseases?

Authors:  Kevin Mouzat; Aleksandra Chudinova; Anne Polge; Jovana Kantar; William Camu; Cédric Raoul; Serge Lumbroso
Journal:  Int J Mol Sci       Date:  2019-08-08       Impact factor: 5.923

10.  DHCR24 exerts neuroprotection upon inflammation-induced neuronal death.

Authors:  Henna Martiskainen; Kaisa M A Paldanius; Teemu Natunen; Mari Takalo; Mikael Marttinen; Stina Leskelä; Nadine Huber; Petra Mäkinen; Enni Bertling; Hiramani Dhungana; Mikko Huuskonen; Paavo Honkakoski; Pirta Hotulainen; Kirsi Rilla; Jari Koistinaho; Hilkka Soininen; Tarja Malm; Annakaisa Haapasalo; Mikko Hiltunen
Journal:  J Neuroinflammation       Date:  2017-11-07       Impact factor: 8.322

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