Evidence map›Paper›PMID 26268310›Full record

ArticleJournal of experimental & clinical cancer research : CR2015

EZH2 is increased in paediatric T-cell acute lymphoblastic leukemia and is a suitable molecular target in combination treatment approaches.

V D'Angelo, A Iannotta, M Ramaglia, A Lombardi, M R Zarone, V Desiderio, M C Affinita, G Pecoraro, M Di Martino, P Indolfi and 2 more

Open access · goldAbstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

16 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. Review
  3. Aberrant stem cell and developmental programs in pediatric leukemia.Frontiers in cell and developmental biology · 2024
    Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Chromatin-Remodeled State in Lymphoma.Current hematologic malignancy reports · 2019
    Review
  13. Article
  14. Review
  15. Article
  16. 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 1 institution in 1 country.

V D'AngeloDepartment of Woman, Child and General and Specialized Surgery, Pediatric Oncology Unit - Second University of Naples, Via Luigi De Crecchio 4, 80138, Naples, Italy. velia.dangelo@unina2.it.
A IannottaDepartment of Woman, Child and General and Specialized Surgery, Pediatric Oncology Unit - Second University of Naples, Via Luigi De Crecchio 4, 80138, Naples, Italy. adriana.iannotta@unina2.it.
M RamagliaDepartment of Woman, Child and General and Specialized Surgery, Pediatric Oncology Unit - Second University of Naples, Via Luigi De Crecchio 4, 80138, Naples, Italy. maria.ramaglia@unina2.it.
A LombardiDepartment of Biochemistry, Biophysics and General Pathology, Second University of Naples, Via S.M. Costantinopoli, 16, 80138, Naples, Italy. angela.lombardi@unina2.it.
M R ZaroneDepartment of Biochemistry, Biophysics and General Pathology, Second University of Naples, Via S.M. Costantinopoli, 16, 80138, Naples, Italy. mayra.zarone@alice.it.
V DesiderioDepartment of Experimental Medicine, Section of Biotechnology and Medical Histology and Embryology, Second University of Naples, Naples, Italy. vincenzo.desiderio@unina2.it.
M C AffinitaDepartment of Woman, Child and General and Specialized Surgery, Pediatric Oncology Unit - Second University of Naples, Via Luigi De Crecchio 4, 80138, Naples, Italy. draffinita@gmail.com.
G PecoraroDepartment of Woman, Child and General and Specialized Surgery, Pediatric Oncology Unit - Second University of Naples, Via Luigi De Crecchio 4, 80138, Naples, Italy. drgiuliapecoraro@gmail.com.
M Di MartinoDepartment of Woman, Child and General and Specialized Surgery, Pediatric Oncology Unit - Second University of Naples, Via Luigi De Crecchio 4, 80138, Naples, Italy. martinadimartino@libero.it.
P IndolfiDepartment of Woman, Child and General and Specialized Surgery, Pediatric Oncology Unit - Second University of Naples, Via Luigi De Crecchio 4, 80138, Naples, Italy. paolo.indolfi@unina2.it.
F CasaleDepartment of Woman, Child and General and Specialized Surgery, Pediatric Oncology Unit - Second University of Naples, Via Luigi De Crecchio 4, 80138, Naples, Italy. fiorina.casale@unina2.it.
M CaragliaDepartment of Biochemistry, Biophysics and General Pathology, Second University of Naples, Via S.M. Costantinopoli, 16, 80138, Naples, Italy. michele.caraglia@unina2.it.
University of Campania "Luigi Vanvitelli" · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundT-cell Acute Lymphoblastic Leukemia (ALL) represents about 10-15 % of pediatric ALL cases. EZH2, one of the components of Polycomb group proteins (PRC2) complex, catalyzes the trimethylation of histone H3 lysine 27 that is associated with transcriptional repression and tumor development.

methodsWe examined the expression levels of PRC2 complex in primary samples of T cells ALL at diagnosis by western blotting and real time PCR. We evaluated the effect of 3-deazaneplanocin-A (DZNep), an EZH2 inhibitor, alone and in combination with Daunoblastine on cell viability, apoptotic death and cell cycle distribution of T cell established Jurkat cell line.

resultsEZH2 was expressed in 75 % samples at different extents mainly with high expression level. SUZ12 was expressed in 60 % samples and EED in all samples, respectively. The Kaplan-Meier analysis shows that T-ALL expressing EZH2 had a lower probability of disease-free survival (DFS) compared to T-ALL negative for EZH2 (23 % vs 100 %) (p = 0.01). The EZH2 inhibitor DZNep used in combination with Daunoblastine was synergistic in inducing growth inhibition and increasing the apoptosis in T-ALL Jurkat cells at 48 and 72 h paralleled by EZH2 decreased expression. Moreover, the combination decreased the activity of Erk-1/2 proliferation enzymes with no effects on Akt survival pathway.

conclusionsThe evaluation of EZH2 expression in pediatric T-ALL can be useful in predict the clinical outcome of the patients and EZH2 can be a useful target to improve the efficacy of conventional chemotherapy in this subset of patients with bad prognosis.

Indexed as

Cell Line, TumorCell ProliferationChildEnhancer of Zeste Homolog 2 ProteinEpigenesis, GeneticFemaleGene ExpressionHumansMalePolycomb Repressive Complex 2Precursor T-Cell Lymphoblastic Leukemia-LymphomaEnhancer of Zeste Homolog 2 ProteinEZH2 protein, humanPolycomb Repressive Complex 2

Identifiers

PMID26268310
PMCPMC4535295
OpenAlexW2141101935

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.