Lymphocytes of Patients with Alzheimer's Disease Display Different DNA Damage Repair Kinetics and Expression Profiles of DNA Repair and Stress Response Genes

被引:19
作者
Leandro, Giovana S. [1 ]
Lobo, Romulo R. [2 ]
Oliveira, Douglas V. N. P. [1 ]
Moriguti, Julio C. [2 ]
Sakamoto-Hojo, Elza T. [1 ,3 ]
机构
[1] Univ Sao Paulo, Fac Med Ribeirao Preto, Dept Genet, BR-14049900 Ribeirao Preto, SP, Brazil
[2] Univ Sao Paulo, Fac Med Ribeirao Preto, Dept Clin Med, BR-14049900 Ribeirao Preto, SP, Brazil
[3] Univ Sao Paulo, Fac Philosophy Sci & Letters Ribeirao Preto, Dept Biol, BR-14040901 Ribeirao Preto, SP, Brazil
来源
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES | 2013年 / 14卷 / 06期
基金
巴西圣保罗研究基金会;
关键词
Alzheimer's disease; DNA repair; oxidative stress; FANCONI-ANEMIA PROTEINS; OXIDATIVE DAMAGE; COMET ASSAY; PERIPHERAL LYMPHOCYTES; HYDROGEN-PEROXIDE; ELEVATED LEVELS; MUTT PROTEIN; IN-VIVO; P53; GENETICS;
D O I
10.3390/ijms140612380
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Alzheimer's disease (AD) is a progressive neurodegenerative disorder, characterized by loss of memory and cognitive capacity. Given the limitations to analyze brain cells, it is important to study whether peripheral lymphocytes can provide biological markers for AD, an interesting approach, once they represent the overall condition of the organism. To that extent, we sought to find whether lymphocytes of AD patients present DNA damage and repair kinetics different from those found in elderly matched controls (EC group) under in vitro treatment with hydrogen peroxide. We found that AD patient cells indeed showed an altered DNA repair kinetics (comet assay). Real-time quantitative analysis of genes associated with DNA stress response also showed that FANCG and CDKN1A are upregulated in AD, while MTH1 is downregulated, compared with the control group. In contrast, the expression of ATM, ATR and FEN1 genes does not seem to differ between these groups. Interestingly, TP53 protein expression was increased in AD patients. Therefore, we found that kinetics of the stress response in the DNA were significantly different in AD patients, supporting the hypothesis that repair pathways may be compromised in AD and that peripheral lymphocytes can reveal this condition.
引用
收藏
页码:12380 / 12400
页数:21
相关论文
共 50 条
  • [31] Polymorphisms of DNA repair and oxidative stress genes in B-cell lymphoma patients
    Fabisiewicz, Anna
    Pacholewicz, Katarzyna
    Paszkiewicz-Kozik, Ewa
    Walewski, Jan
    Siedlecki, Janusz A.
    BIOMEDICAL REPORTS, 2013, 1 (01) : 151 - 155
  • [32] Oxidative Stress, DNA Damage and DNA Repair in Female Patients with Diabetes Mellitus Type 2
    Grindel, Annemarie
    Guggenberger, Bianca
    Eichberger, Lukas
    Poeppelmeyer, Christina
    Gschaider, Michaela
    Tosevska, Anela
    Mare, George
    Briskey, David
    Brath, Helmut
    Wagner, Karl-Heinz
    PLOS ONE, 2016, 11 (09):
  • [33] Expression of DNA repair and metabolic genes in response to a flavonoid-rich diet
    Guarrera, Simonetta
    Sacerdote, Carlotta
    Fiorini, Laura
    Marsala, Rosa
    Polidoro, Silvia
    Gainberini, Sara
    Saletta, Federica
    Malaveille, Christian
    Talaska, Glenn
    Vineis, Paolo
    Matullo, Giuseppe
    BRITISH JOURNAL OF NUTRITION, 2007, 98 (03) : 525 - 533
  • [34] NAD+ supplementation normalizes key Alzheimer's features and DNA damage responses in a new AD mouse model with introduced DNA repair deficiency
    Hou, Yujun
    Lautrup, Sofie
    Cordonnier, Stephanie
    Wang, Yue
    Croteau, Deborah L.
    Zavala, Eduardo
    Zhang, Yongqing
    Moritoh, Kanako
    O'Connell, Jennifer F.
    Baptiste, Beverly A.
    Stevnsner, Tinna V.
    Mattson, Mark P.
    Bohr, Vilhelm A.
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2018, 115 (08) : E1876 - E1885
  • [35] DNA damage and repair in lymphocytes of normal individuals and cancer patients: Studies by the comet assay and micronucleus tests
    Palyvoda, O
    Polanska, J
    Wygoda, A
    Rzeszowska-Wolny, J
    ACTA BIOCHIMICA POLONICA, 2003, 50 (01) : 181 - 190
  • [36] DNA Damage/Repair and Polymorphism of the hOGG1 Gene in Lymphocytes of AMD Patients
    Wozniak, Katarzyna
    Szaflik, Jacek P.
    Zaras, Malgorzata
    Sklodowska, Anna
    Janik-Papis, Katarzyna
    Poplawski, Tomasz R.
    Blasiak, Janusz
    Szaflik, Jerzy
    JOURNAL OF BIOMEDICINE AND BIOTECHNOLOGY, 2009,
  • [37] Decreased expression level of BER genes in Alzheimer's disease patients is not derivative of their DNA methylation status
    Sliwinska, Agnieszka
    Sitarek, Przemyslaw
    Toma, Monika
    Czarny, Piotr
    Synowiec, Ewelina
    Krupa, Renata
    Wigner, Paulina
    Bialek, Katarzyna
    Kwiatkowski, Dominik
    Korycinska, Anna
    Majsterek, Ireneusz
    Szemraj, Janusz
    Galecki, Piotr
    Sliwinski, Tomasz
    PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 2017, 79 : 311 - 316
  • [38] Gypenosides Causes DNA Damage and Inhibits Expression of DNA Repair Genes of Human Oral Cancer SAS Cells
    Lu, Kung-Wen
    Chen, Jung-Chou
    Lai, Tung-Yuan
    Yang, Jai-Sing
    Weng, Shu-Wen
    Ma, Yi-Shih
    Tang, Nou-Ying
    Lu, Pei-Jung
    Weng, Jing-Ru
    Chung, Jing-Gung
    IN VIVO, 2010, 24 (03): : 285 - 289
  • [39] Paternal exposure to cyclophosphamide induces DNA damage and alters the expression of DNA repair genes in the rat preimplantation embryo
    Harrouk, W
    Codrington, A
    Vinson, R
    Robaire, B
    Hales, BF
    MUTATION RESEARCH-DNA REPAIR, 2000, 461 (03): : 229 - 241
  • [40] Oxidative DNA damage and reduced expression of DNA repair genes: Role in primary open angle glaucoma (POAG)
    Mohanty, Kuldeep
    Dada, Rima
    Dada, Tanuj
    OPHTHALMIC GENETICS, 2017, 38 (05) : 446 - 450