Evidence map›Paper›PMID 25161998›Full record

ArticleBioMed research international2014

PARP1-driven apoptosis in chronic lymphocytic leukemia.

Panagiotis T Diamantopoulos, Maria Sofotasiou, Vasiliki Papadopoulou, Katerina Polonyfi, Theodoros Iliakis, Nora-Athina Viniou

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

24 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
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  7. Review
  8. Anti-tumor effect of berberine on chronic lymphocytic leukemia cells.Medical oncology (Northwood, London, England) · 2022
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  12. Identification of 20(Oxidative medicine and cellular longevity · 2022
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  18. Effects of DNA Damage and Oxidative Stress in Human Bronchial Epithelial Cells Exposed to PMInternational journal of environmental research and public health · 2020
    Article
  19. Article
  20. 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

6 authors at 2 institutions in 1 country.

Panagiotis T DiamantopoulosDepartment of Internal Medicine, Hematology Unit, Laikon General Hospital, National and Kapodistrian University of Athens, 11527 Athens, Greece.
Maria SofotasiouDepartment of Internal Medicine, Hematology Unit, Laikon General Hospital, National and Kapodistrian University of Athens, 11527 Athens, Greece.
Vasiliki PapadopoulouDepartment of Internal Medicine, Hematology Unit, Laikon General Hospital, National and Kapodistrian University of Athens, 11527 Athens, Greece.
Katerina PolonyfiDepartment of Internal Medicine, Hematology Unit, Laikon General Hospital, National and Kapodistrian University of Athens, 11527 Athens, Greece.
Theodoros IliakisDepartment of Internal Medicine, Hematology Unit, Laikon General Hospital, National and Kapodistrian University of Athens, 11527 Athens, Greece.
Nora-Athina ViniouDepartment of Internal Medicine, Hematology Unit, Laikon General Hospital, National and Kapodistrian University of Athens, 11527 Athens, Greece.
Laiko General Hospital of Athens · GRNational and Kapodistrian University of Athens · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic lymphocytic leukemia (CLL) is considered a malignancy resulting from defects in apoptosis. For this reason, targeting apoptotic pathways in CLL may be valuable for its management. Poly [ADP-ribose] polymerase 1 (PARP1) is the main member of a family of nuclear enzymes that act as DNA damage sensors. Through binding on DNA damaged structures, PARP1 recruits repair enzymes and serves as a survival factor, but if the damage is severe enough, its action may lead the cell to apoptosis through caspase activation, or necrosis. We measured the PARP1 mRNA and protein pretreatment levels in 26 patients with CLL and the corresponding posttreatment levels in 15 patients after 3 cycles of immunochemotherapy, as well as in 15 healthy blood donors. No difference was found between the pre- and posttreatment levels of PARP1, but we found a statistically significant relative increase of the 89 kDa fragment of PARP1 that is cleaved by caspases in the posttreatment samples, indicating PARP1-related apoptosis in CLL patients after treatment. Our findings constitute an important step in the field, especially in the era of PARP1 inhibitors, and may serve as a base for future clinical trials with these agents in CLL.

Indexed as

AgedAged, 80 and overApoptosisDNA DamageFemaleGene Expression Regulation, NeoplasticHumansLeukemia, Lymphocytic, Chronic, B-CellMaleMiddle AgedPoly (ADP-Ribose) Polymerase-1Poly(ADP-ribose) PolymerasesProteolysisPARP1 protein, humanPoly (ADP-Ribose) Polymerase-1Poly(ADP-ribose) Polymerases

Identifiers

PMID25161998
PMCPMC4137605
OpenAlexW1970292996

What OpenQuestion holds

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Registered trials

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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.