Evidence map›Paper›PMID 12659690›Full record

ArticleNeoplasia (New York, N.Y.)

Telomerase activity and genetic alterations in primary breast carcinomas.

Anna Papadopoulou, Theoni Trangas, Manuel R Teixeira, Sverre Heim, Euthimios Dimitriadis, Haroula Tsarouha, Johan A Andersen, Evangelos Evangelou, Panayiotis Ioannidis, Niki J Agnantis and 1 more

Open access · goldAbstract read
In one paragraph

Article in Neoplasia (New York, N.Y.). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
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  4. Review
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

11 authors at 6 institutions in 5 countries.

Anna PapadopoulouDepartment of Genetics, Saint Savas Hospital, Athens, Greece.
Theoni Trangas
Manuel R Teixeira
Sverre Heim
Euthimios Dimitriadis
Haroula Tsarouha
Johan A Andersen
Evangelos Evangelou
Panayiotis Ioannidis
Niki J Agnantis
Nikos Pandis
St Savas Hospital · GRInstitute for Medical Informatics and Biostatistics · CHInstituto Português de Oncologia Francisco Gentil · PTNational and Kapodistrian University of Athens · GROdense University Hospital · DKUniversity of Ioannina · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It has been proposed that the structural and numerical chromosome abnormalities recorded in breast cancer could be the result of telomere dysfunction and that telomerase is activated de novo to provide a survival mechanism curtailing further chromosomal aberrations. However, recent in vivo and in vitro data show that the ectopic expression of telomerase promotes tumorigenesis via a telomere length-independent mechanism. In this study, the relation between telomerase expression and the extent of chromosomal aberrations was investigated in 62 primary breast carcinomas. Telomerase activity was measured using a polymerase chain reaction-based telomeric repeat amplification protocol assay and 92% of the tumors were found to express telomerase with a relative activity ranging from 0 to 3839.6. Genetic alterations were determined by G-banding and comparative genomic hybridization analysis and 97% of the tumors exhibited chromosomal aberrations ranging from 0 to 44 (average: 10.98). In the overall series, the relationship between telomerase activity levels and genetic changes could be best described by a quadratic model, whereas in tumors with below-average genetic alteration numbers, a significant positive association was recorded between the two variables (coefficient=0.374, P=.017). The relationship between telomerase activity levels and the extent of genetic alteration may reflect the complex effect of telomerase activation upon tumor progression in breast carcinomas.

Indexed as

AdultAgedAged, 80 and overAge FactorsBreast NeoplasmsCarcinomaCell Line, TumorChromosome AberrationsChromosome BandingCytogeneticsDisease ProgressionFemaleHumansMiddle AgedTelomeraseTime FactorsTelomerase

Identifiers

PMID12659690
PMCPMC1502403
OpenAlexW1979593261

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.