Evidence map›Paper›PMID 25595889›Full record

ArticleOncotarget2015

Intratumoral diversity of telomere length in individual neuroblastoma tumors.

Annalisa Pezzolo, Angela Pistorio, Claudio Gambini, Riccardo Haupt, Manuela Ferraro, Giovanni Erminio, Bruno De Bernardi, Alberto Garaventa, Vito Pistoia

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 2 pooled it
2.4field-weighted citation impact, top 13% 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

33 citing papers in PubMed, 2 syntheses or guidelines pooled it, 47 citations in OpenAlex.

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  16. Molecular Genetics in Neuroblastoma Prognosis.Children (Basel, Switzerland) · 2021
    Review
  17. Review
  18. Drivers of dynamic intratumor heterogeneity and phenotypic plasticity.American journal of physiology. Cell physiology · 2021
    Review
  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

9 authors at 1 institution in 1 country.

Annalisa PezzoloLaboratorio di Oncologia, Istituto Giannina Gaslini, Genova, Italy.
Angela PistorioEpidemiologia e Biostatistica, Istituto Giannina Gaslini, Genova, Italy.
Claudio GambiniLaboratorio di Anatomia Patologica, Istituto Giannina Gaslini, Genova, Italy.
Riccardo HauptEpidemiologia e Biostatistica, Istituto Giannina Gaslini, Genova, Italy.
Manuela FerraroLaboratorio di Anatomia Patologica, Istituto Giannina Gaslini, Genova, Italy.
Giovanni ErminioEpidemiologia e Biostatistica, Istituto Giannina Gaslini, Genova, Italy.
Bruno De BernardiDipartimento di Emato-Oncologia Pediatrica, Istituto Giannina Gaslini, Genova, Italy.
Alberto GaraventaDipartimento di Emato-Oncologia Pediatrica, Istituto Giannina Gaslini, Genova, Italy.
Vito PistoiaLaboratorio di Oncologia, Istituto Giannina Gaslini, Genova, Italy.
Istituto Giannina Gaslini · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The purpose of the work was to investigate telomere length (TL) and mechanisms involved in TL maintenance in individual neuroblastoma (NB) tumors. Primary NB tumors from 102 patients, ninety Italian and twelve Spanish, diagnosed from 2000 to 2008 were studied. TL was investigated by quantitative fluorescence in situ hybridization (IQ-FISH) that allows to analyze individual cells in paraffin-embedded tissues. Fluorescence intensity of chromosome 2 centromere was used as internal control to normalize TL values to ploidy. Human telomerase reverse transcriptase (hTERT) expression was detected by immunofluorescence in 99/102 NB specimens.The main findings are the following: 1) two intratumoral subpopulations of cancer cells displaying telomeres of different length were identified in 32/102 tumors belonging to all stages. 2) hTERT expression was detected in 99/102 tumors, of which 31 displayed high expression and 68 low expression. Alternative lengthening of telomeres (ALT)-mechanism was present in 60/102 tumors, 20 of which showed high hTERT expression. Neither ALT-mechanism nor hTERT expression correlated with heterogeneous TL. 3) High hTERT expression and ALT positivity were associated with significantly reduced Overall Survival. 4) High hTERT expression predicted relapse irrespective of patient age. Intratumoral diversity in TL represents a novel feature in NB.In conclusion, diversity of TL in individual NB tumors was strongly associated with disease progression and death, suggesting that these findings are of translational relevance. The combination of high hTERT expression and ALT positivity may represent a novel biomarker of poor prognosis that deserves further investigation.

Indexed as

Cell Line, TumorDisease-Free SurvivalFemaleHumansMaleNeuroblastomaRetrospective StudiesSurvival AnalysisTelomeraseTelomereTelomeraseALT mechanismneuroblastomatelomerasetelomere length

Identifiers

PMID25595889
PMCPMC4480695
OpenAlexW1881696760

What OpenQuestion holds

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LicenceCC BY
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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.