Evidence map›Paper›PMID 20502937›Full record

ArticleCellular and molecular life sciences : CMLS2010

Activation of ataxia telangiectasia muted under experimental models and human Parkinson's disease.

Antoni Camins, Javier G Pizarro, Daniel Alvira, Javier Gutierrez-Cuesta, Aurelio Vazquez de la Torre, Jaume Folch, Francesc X Sureda, Ester Verdaguer, Felix Junyent, Joaquín Jordán and 2 more

Open access · greenAbstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.4field-weighted citation impact, top 37% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Novel Techniques for Mapping DNA Damage and Repair in the Brain.International journal of molecular sciences · 2024
    Review
  6. Review
  7. DNA Damage-Mediated Neurotoxicity in Parkinson's Disease.International journal of molecular sciences · 2023
    Review
  8. Article
  9. Brain Selective Estrogen Treatment Protects Dopaminergic Neurons and Preserves Behavioral Function in MPTP-induced Mouse Model of Parkinson's Disease.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2021
    Article
  10. Article
  11. Article
  12. DNA double-strand breaks: a potential therapeutic target for neurodegenerative diseases.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2019
    Review
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 5 institutions in 1 country.

Antoni CaminsInstitut de Biomedicina, Centros de Investigación Biomédica en Red de Enfermedades Neurodegenerativas, Universitat de Barcelona, Spain. camins@ub.edu
Javier G Pizarro
Daniel Alvira
Javier Gutierrez-Cuesta
Aurelio Vazquez de la Torre
Jaume Folch
Francesc X Sureda
Ester Verdaguer
Felix Junyent
Joaquín Jordán
Isidre Ferrer
Mercè Pallàs
Universitat de Barcelona · ESBiomedical Research Networking Center on Neurodegenerative Diseases · ESBellvitge University Hospital · ESUniversidad Rovira i Virgili · ESUniversity of Castilla-La Mancha · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the present study we demonstrated that neurotoxin MPP(+)-induced DNA damage is followed by ataxia telangiectasia muted (ATM) activation either in cerebellar granule cells (CGC) or in B65 cell line. In CGC, the selective ATM inhibitor KU-55933 showed neuroprotective effects against MPP(+)-induced neuronal cell loss and apoptosis, lending support to the key role of ATM in experimental models of Parkinson's disease. Likewise, we showed that knockdown of ATM levels in neuroblastoma B65 cells using an ATM-specific siRNA attenuates the phosphorylation of retinoblastoma protein without affecting other cell-cycle proteins involved in the G(0)/G(1) cell-cycle phase. Moreover, we demonstrated DNA damage, in human brain samples of PD patients. These findings support a model in which MPP(+) leads to ATM activation with a subsequent DNA damage response and activation of pRb. Therefore, this study demonstrates a new link between DNA damage by MPP(+) and cell-cycle re-entry through retinoblastoma protein phosphorylation.

Indexed as

1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridineAgedAged, 80 and overAnimalsApoptosisAtaxia Telangiectasia Mutated ProteinsBrainCell CycleCell Cycle ProteinsCell LineCells, CulturedCerebellumDNA-Binding ProteinsDNA DamageFemaleHumans1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine2-morpholin-4-yl-6-thianthren-1-yl-pyran-4-oneAtaxia Telangiectasia Mutated ProteinsATM protein, humanCell Cycle ProteinsDNA-Binding ProteinsMorpholinesNeurotoxinsProtein Serine-Threonine KinasesPyronesTumor Suppressor Proteins

Identifiers

PMID20502937
PMCPMC11115894
OpenAlexW2092647016

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.