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
  • [21] Evaluation of DNA damage in COPD patients and its correlation with polymorphisms in repair genes
    Goncalves da Silva, Andrea Lucia
    da Rosa, Helen Tais
    Karnopp, Thais Evelyn
    Charlier, Clara Forrer
    Ellwanger, Joel Henrique
    Moura, Dinara Jaqueline
    Possuelo, Lia Goncalves
    de Moura Valim, Andreia Rosane
    Guecheva, Temenouga Nikolova
    Pegas Henriques, Joao Antonio
    BMC MEDICAL GENETICS, 2013, 14
  • [22] DNA Damage Repair in Huntington’s Disease and Other Neurodegenerative Diseases
    T. Maiuri
    C. E. Suart
    C. L. K. Hung
    K. J. Graham
    C. A. Barba Bazan
    R. Truant
    Neurotherapeutics, 2019, 16 : 948 - 956
  • [23] An evaluation of the differences in DNA damage in lymphocytes and repair efficiencies in patients with schizophrenia and schizoaffective disorder
    Topak, Osman Zulkif
    Ozdel, Osman
    Dodurga, Yavuz
    Secme, Mucahit
    SCHIZOPHRENIA RESEARCH, 2018, 202 : 99 - 105
  • [24] DNA Damage Repair in Huntington's Disease and Other Neurodegenerative Diseases
    Maiuri, T.
    Suart, C. E.
    Hung, C. L. K.
    Graham, K. J.
    Bazan, C. A. Barba
    Truant, R.
    NEUROTHERAPEUTICS, 2019, 16 (04) : 948 - 956
  • [25] Evidence of aberrant DNA damage response signalling but normal rates of DNA repair in dividing lymphoblasts from patients with schizophrenia
    Catts, Vibeke Sorensen
    Catts, Stanley Victor
    Jablensky, Assen
    Chandler, David
    Weickert, Cynthia Shannon
    Lavin, Martin F.
    WORLD JOURNAL OF BIOLOGICAL PSYCHIATRY, 2012, 13 (02) : 114 - 125
  • [26] Altered DNA base excision repair profile in brain tissue and blood in Alzheimer's disease
    Lillenes, Meryl S.
    Rabano, Alberto
    Stoen, Mari
    Riaz, Tahira
    Misaghian, Dorna
    Mollersen, Linda
    Esbensen, Ying
    Gunther, Clara-Cecilie
    Selnes, Per
    Stenset, Vidar T. V.
    Fladby, Tormod
    Tonjum, Tone
    MOLECULAR BRAIN, 2016, 9
  • [27] Expression signatures of DNA repair genes correlate with survival prognosis of astrocytoma patients
    de Sousa, Juliana Ferreira
    Torrieri, Raul
    Serafim, Rodolfo Bortolozo
    Macedo Di Cristofaro, Luis Fernando
    Escanfella, Fÿbio Dalbon
    Ribeiro, Rodrigo
    Zanette, Dalila Luciola
    Paco-Larson, Maria Luisa
    da Silva, Wilson Araujo, Jr.
    da Cunha Tirapelli, Daniela Pretti
    Neder, Luciano
    Carlotti, Carlos Gilberto, Jr.
    Valente, Valeria
    TUMOR BIOLOGY, 2017, 39 (04)
  • [28] Decoding the Role of Familial Parkinson's Disease-Related Genes in DNA Damage and Repair
    Li, Yao-Lin
    Wang, Zhong-Xuan
    Ying, Chang-Zhou
    Zhang, Bao-Rong
    Pu, Jia-Li
    AGING AND DISEASE, 2022, 13 (05): : 1405 - 1412
  • [29] DNA damage and repair in Parkinson's disease: Recent advances and new opportunities
    Gonzalez-Hunt, Claudia P.
    Sanders, Laurie H.
    JOURNAL OF NEUROSCIENCE RESEARCH, 2021, 99 (01) : 180 - 189
  • [30] 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