Telomerase expression in amyotrophic lateral sclerosis (ALS) patients

被引:29
|
作者
De Felice, Bruna [1 ]
Annunziata, Anna [2 ]
Fiorentino, Giuseppe [2 ]
Manfellotto, Francesco [1 ]
D'Alessandro, Raffaella [1 ]
Marino, Rita [3 ]
Borra, Marco [3 ]
Biffali, Elio [3 ]
机构
[1] Univ Naples 2, Dept Environm Biol & Pharmaceut Sci & Technol, DISTABIF, I-81100 Caserta, Italy
[2] Monaldi Hosp, Div Resp Physiopathol, Naples, Italy
[3] Stn Zool Anton Dohrn, Naples, Italy
关键词
CATALYTIC SUBUNIT; REVERSE-TRANSCRIPTASE; GENE-EXPRESSION; BRAIN-INJURY; CELL-DEATH; P53; NEURONS; PROTECTS; SENESCENCE; APOPTOSIS;
D O I
10.1038/jhg.2014.72
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Telomerase and telomeric complex have been linked to a variety of disease states related to neurological dysfunction. In amyotrophic lateral sclerosis (ALS) patients, telomerase activity, as human telomerase reverse transcriptase (hTERT) expression, has not been characterized yet. Here, for the first time, we characterized telomerase and related pathway in blood sample and spinal cord from ALS patients compared with healthy controls. We found that hTERT expression level was significantly lower in ALS patients and was correlated either to p53 mRNA expression or p21 expression, pointing out the hypothesis that telomerase inhibition could be a pathogenetic contributor to neurodegeneration in ALS. As a consequence of the reduced telomerase activity, we identified shorter telomeres in leukocytes from sporadic ALS patients compared with healthy control group.
引用
收藏
页码:555 / 561
页数:7
相关论文
共 50 条
  • [1] Telomerase expression in amyotrophic lateral sclerosis (ALS) patients
    Bruna De Felice
    Anna Annunziata
    Giuseppe Fiorentino
    Francesco Manfellotto
    Raffaella D'Alessandro
    Rita Marino
    Marco Borra
    Elio Biffali
    [J]. Journal of Human Genetics, 2014, 59 : 555 - 561
  • [2] Amyotrophic lateral sclerosis (ALS)
    Silani, V.
    [J]. EUROPEAN JOURNAL OF NEUROLOGY, 2017, 24 : 4 - 4
  • [3] Parkinsonian features in patients with amyotrophic lateral sclerosis (ALS)
    Szczudlik, P.
    Ostrowska, M.
    Tomik, B.
    Kwiecinski, H.
    [J]. EUROPEAN JOURNAL OF NEUROLOGY, 2008, 15 : 350 - 351
  • [4] PSYCHOLOGICAL CHARACTERISTICS OF PATIENTS WITH AMYOTROPHIC LATERAL SCLEROSIS (ALS)
    HOUPT, JL
    GOULD, BS
    NORRIS, FH
    [J]. PSYCHOSOMATIC MEDICINE, 1977, 39 (05) : 299 - 303
  • [5] Gastrointestinal Dysmotility in Patients with Amyotrophic Lateral Sclerosis (ALS)
    Schaff, Christina Martin
    Heiman-Patterson, Terry
    Deboo, Anahita
    Barr, Christine
    [J]. MUSCLE & NERVE, 2022, 66 : S26 - S26
  • [6] Home care of patients with amyotrophic lateral sclerosis (ALS)
    Krivickas, LS
    Shockley, L
    Mitsumoto, H
    [J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 1997, 152 : S82 - S89
  • [7] Excessive exercising in patients with amyotrophic lateral sclerosis (als)
    Ebel, Leonie
    Kammeyer, Johanna
    Petri, Susanne
    Mueller, Astrid
    De Zwaan, Martina
    [J]. JOURNAL OF BEHAVIORAL ADDICTIONS, 2017, 6 : 65 - 65
  • [8] POLIOVIRUS AND AMYOTROPHIC LATERAL SCLEROSIS (ALS)
    GANN, KL
    VIOLA, MV
    [J]. CLINICAL RESEARCH, 1978, 26 (04): : A626 - A626
  • [9] Amyotrophic Lateral Sclerosis(ALS):Will There Be A Cure?
    GUAN Teng
    ZHANG Xiao-sha
    ZHOU Ting
    WANG Yu-tian
    孔吉明
    [J]. 神经药理学报, 2019, 9(Z1) (Z1) : 28 - 30
  • [10] NEW CLASSIFICATION OF AMYOTROPHIC LATERAL SCLEROSIS (ALS) AND FAMILIAL AMYOTROPHIC LATERAL SCLEROSIS (FALS)
    MORARIU, MA
    [J]. DISEASES OF THE NERVOUS SYSTEM, 1977, 38 (06): : 468 - 469