Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/24498
Title: Evaluation of GammaH2AX in Buccal Cells as a Molecular Biomarker of DNA Damage in Alzheimer's Disease in the AIBL Study of Ageing.
Austin Authors: Siddiqui, Mohammad Sabbir;Francois, Maxime;Rainey-Smith, Stephanie;Martins, Ralph;Masters, Colin L ;Ames, David;Rowe, Christopher C ;Macaulay, Lance S;Fenech, Michael F;Leifert, Wayne R
Affiliation: CSIRO Health and Biosecurity, Molecular Diagnostic Solutions, Adelaide SA5005, Australia
School of Agriculture, Food & Wine, the University of Adelaide, Urrbrae 5064, Australia
School of Biological Sciences, the University of Adelaide, Adelaide SA 5005, Australia
Centre of Excellence for Alzheimer's Disease Research & Care, School of Medical Sciences, Edith Cowan University, Joondalup 6027, Australia
Sir James McCusker Alzheimer's Disease Research Unit (Hollywood Private Hospital), Nedlands 6009, Australia
The Florey Institute of Neuroscience and Mental Health, The University of Melbourne, Parkville 3052, Australia
National Ageing Research Institute, Parkville 3052, Australia
Molecular Imaging and Therapy
Issue Date: 6-Aug-2020
metadata.dc.date: 2020-08-06
Publication information: Life 2020; 10(8): 141
Abstract: In response to double-stranded breaks (DSBs) in chromosomal DNA, H2AX (a member of histone H2A family) becomes phosphorylated to form γH2AX. Although increased levels of γH2AX have been reported in the neuronal nuclei of Alzheimer's disease (AD) patients, the understanding of γH2AX responses in buccal nuclei of individuals with mild cognitive impairment (MCI) and AD remain unexplored. In the current study, endogenous γH2AX was measured in buccal cell nuclei from MCI (n = 18) or AD (n = 16) patients and in healthy controls (n = 17) using laser scanning cytometry (LSC). The γH2AX level was significantly elevated in nuclei of the AD group compared to the MCI and control group, and there was a concomitant increase in P-trend for γH2AX from the control group through MCI to the AD group. Receiver-operating characteristic curves were carried out for different γH2AX parameters; γH2AX in nuclei resulted in the greatest area under the curve value of 0.7794 (p = 0.0062) with 75% sensitivity and 70% specificity for the identification of AD patients from control. In addition, nuclear circularity (a measure of irregular nuclear shape) was significantly higher in the buccal cell nuclei from the AD group compared with the MCI and control groups. Additionally, there was a positive correlation between the nuclear circularity and γH2AX signals. The results indicated that increased DNA damage is associated with AD.
URI: https://ahro.austin.org.au/austinjspui/handle/1/24498
DOI: 10.3390/life10080141
ORCID: 0000-0003-1317-1506
0000-0003-0535-7327
PubMed URL: 32781776
ISSN: 2075-1729
Type: Journal Article
Subjects: Alzheimer’s disease
DNA damage
mild cognitive impairment
senescence
γH2AX
Appears in Collections:Journal articles

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