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Change in INSR, APBA2 and IDE Gene Expressions in Brains of Alzheimer's Disease Patients.

Title: Change in INSR, APBA2 and IDE Gene Expressions in Brains of Alzheimer's Disease Patients.
Authors: da Costa IB; Marília School of Medicine (Faculdade de Medicina de Marília), Marília Sao Paulo. Brazil.; de Labio RW; Marília School of Medicine (Faculdade de Medicina de Marília), Marília Sao Paulo. Brazil.; Rasmussen LT; Universidade do Sagrado Coracao, Bauru, Sao Paulo. Brazil.; Viani GA; Marília School of Medicine (Faculdade de Medicina de Marília), Marília Sao Paulo. Brazil.; Chen E; Federal University of Sao Paulo (Universidade Federal de Sao Paulo), Sao Paulo. Brazil.; Villares J; Federal University of Sao Paulo (Universidade Federal de Sao Paulo), Sao Paulo. Brazil.; Turecki G; Bell Canada Brain Bank, Douglas Mental Health University Institute, Montreal Quebec. Canada.; Smith MAC; Federal University of Sao Paulo (Universidade Federal de Sao Paulo), Sao Paulo. Brazil.; Payao SLM; Laboratório de Genética, Hemocentro, FAMEMA, Rua Lourival Freire, 240, Bairro Fragata, CEP 17519-050, Marília, Sao Paulo. Brazil.
Source: Current Alzheimer research [Curr Alzheimer Res] 2017; Vol. 14 (7), pp. 760-765.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Language: English
Journal Info: Publisher: Bentham Science Publishers Country of Publication: United Arab Emirates NLM ID: 101208441 Publication Model: Print Cited Medium: Internet ISSN: 1875-5828 (Electronic) Linking ISSN: 15672050 NLM ISO Abbreviation: Curr Alzheimer Res Subsets: MEDLINE
Imprint Name(s): Original Publication: Saif Zone, Sharjah, U.A.E. ; San Francisco, CA : Bentham Science Publishers, c2004-
MeSH Terms: Alzheimer Disease/*pathology ; Antigens, CD/*metabolism ; Brain/*metabolism ; Cadherins/*metabolism ; Carrier Proteins/*metabolism ; Gene Expression/*physiology ; Insulysin/*metabolism ; Nerve Tissue Proteins/*metabolism ; Receptor, Insulin/*metabolism; Antigens, CD/genetics ; Apolipoprotein E4/genetics ; Cadherins/genetics ; Carrier Proteins/genetics ; Insulysin/genetics ; Nerve Tissue Proteins/genetics ; RNA, Messenger/metabolism ; Receptor, Insulin/genetics ; Aged ; Aged, 80 and over ; Analysis of Variance ; Female ; Humans ; Male
Abstract: Background: Alzheimer's disease (AD) is defined as a progressive and irreversible neurodegenerative disorder, the onset of which is mainly characterized by decreased cognition, memory loss, and mental confusion.; Objective: This study sought to quantify mRNA expression of the APBA2, INSR and IDE genes in brain samples from patients with AD and controls.; Methods: We investigated the mRNA expression of the APBA2, INSR and IDE genes in 150 RNA samples from entorhinal cortex, auditory cortex, and the hippocampus of individuals with AD and elderly controls using real time PCR. APOE genotypes were determined by PCR-RFLP.; Results: When the total brain samples were analyzed collectively, a decrease in IDE gene expression was found in AD patients relative to healthy elderly controls. However, when the samples were analyzed separately according to the region of the brain, there was a significant upregulation of INSR expression in the hippocampus and the entorhinal cortex in the AD patient group. We did not observe any statistical differences when gene expression was compared in the different regions of the brain of AD patients. When the E4 allele of apolipoprotein-E was considered in AD patients, the presence of this allele was found to be associated with decreased APBA2 gene expression. The same analysis using the INSR and IDE genes showed no significant statistical differences.; Conclusion: These results support the hypothesis that APBA2, IDE, and particularly INSR gene expression in different areas of Alzheimer's patient's brains could represent new markers for use in clinical diagnoses in the near future.; (Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.org.)
Contributed Indexing: Keywords: APBA2; Alzheimer's disease; IDE; INSR; brain; gene expression
Substance Nomenclature: 0 (APBA2 protein, human); 0 (Antigens, CD); 0 (Apolipoprotein E4); 0 (Cadherins); 0 (Carrier Proteins); 0 (Nerve Tissue Proteins); 0 (RNA, Messenger); EC 2.7.10.1 (INSR protein, human); EC 2.7.10.1 (Receptor, Insulin); EC 3.4.24.56 (Insulysin)
Entry Date(s): Date Created: 20170207 Date Completed: 20180410 Latest Revision: 20180510
Update Code: 20260130
DOI: 10.2174/1567205014666170203100734
PMID: 28164769
Database: MEDLINE

Journal Article; Research Support, Non-U.S. Gov't