Literature DB >> 19914341

P53-mediated G(1)/S checkpoint dysfunction in lymphocytes from Alzheimer's disease patients.

Xiaoying Zhou1, Jianping Jia.   

Abstract

To date, Alzheimer disease (AD) is still difficult to be diagnosed in its earliest stage. The cell cycle aberrations may be the earliest neuropathological events detected in AD thus far. The cell cycle regulatory failure in AD occurring at "G(1)/S transition checkpoint" which is mediated by the tumor suppressor protein p53 has been identified. Herein, we observed the response of activated lymphocytes to G(1)/S transition blocker to assess the G(1)/S checkpoint function and the p53 conformation state adopted in lymphocytes from AD patients and healthy non-AD controls. We found that the activated lymphocytes from AD patients were less sensitive to G(1)/S transition blocker than those from controls, indicating that the G(1)/S checkpoint failed to function well in AD lymphocytes. In addition, AD cells specifically expressed an anomalous conformationally mutant-like p53 that made these cells distinct from lymphocytes of controls. We speculated that the altered conformational p53 probably be responsible for G(1)/S checkpoint dysfunction in AD cells. Our hypothesis was supported by the results that G(1)/S checkpoint dysfunction was not restricted to neurons in AD patients, but also occurred in peripheral lymphocytes. Two potential biomarkers were indicated in blood lymphocytes from AD patients: the G(1)/S checkpoint dysfunction and the conformationally mutant-like p53 protein. Copyright 2009 Elsevier Ireland Ltd. All rights reserved.

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Year:  2009        PMID: 19914341     DOI: 10.1016/j.neulet.2009.11.024

Source DB:  PubMed          Journal:  Neurosci Lett        ISSN: 0304-3940            Impact factor:   3.046


  12 in total

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4.  Conformational altered p53 as an early marker of oxidative stress in Alzheimer's disease.

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5.  Two Blood Monocytic Biomarkers (CCL15 and p21) Combined with the Mini-Mental State Examination Discriminate Alzheimer's Disease Patients from Healthy Subjects.

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6.  CHIP stabilizes amyloid precursor protein via proteasomal degradation and p53-mediated trans-repression of β-secretase.

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7.  Dysfunction of the mTOR pathway is a risk factor for Alzheimer's disease.

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8.  Calmodulin levels in blood cells as a potential biomarker of Alzheimer's disease.

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9.  PARP-1 and p53 Regulate the Increased Susceptibility to Oxidative Death of Lymphocytes from MCI and AD Patients.

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10.  Identification of Methylated Gene Biomarkers in Patients with Alzheimer's Disease Based on Machine Learning.

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Journal:  Biomed Res Int       Date:  2020-03-26       Impact factor: 3.411

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