Evidence map›Paper›PMID 31934157›Full record

ArticleInternational journal of clinical and experimental pathology2019

Scanning all chromosomal abnormalities with microarray-based comparative genomic hybridization in differential diagnosis of pediatric cancers.

Hulya Tosun Yildirim, Safiye Aktas, Gulden Diniz, Tekincan Cagri Aktas, Burcin Baran, Serdar Bayrak, Zekiye Altun, Yasemin Cakir, Nur Olgun

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 81% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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 3 institutions in 2 countries.

Hulya Tosun YildirimDepartment of Pathology, Antalya Education and Research Hospital, Health Sciences University Antalya, Turkey.
Safiye AktasOncology Institute, Department of Basic Oncology, Dokuz Eylul University Izmir, Turkey.
Gulden DinizDepartment of Pathology, Izmir Democracy University Izmir, Turkey.
Tekincan Cagri AktasOncology Institute, Department of Basic Oncology, Dokuz Eylul University Izmir, Turkey.
Burcin BaranOncology Institute, Department of Basic Oncology, Dokuz Eylul University Izmir, Turkey.
Serdar BayrakOncology Institute, Department of Basic Oncology, Dokuz Eylul University Izmir, Turkey.
Zekiye AltunOncology Institute, Department of Basic Oncology, Dokuz Eylul University Izmir, Turkey.
Yasemin CakirOncology Institute, Department of Basic Oncology, Dokuz Eylul University Izmir, Turkey.
Nur OlgunOncology Institute, Department of Basic Oncology, Dokuz Eylul University Izmir, Turkey.
Dokuz Eylül University · TRAntalya Bilim University · TRIzmir University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveDespite conventional histopathological and immunohistochemical methods, difficulties may be experienced in the differential diagnosis of pediatric cancers, especially in small round-cell undifferentiated tumors. In these cases, the determination of chromosomal abnormalities may be helpful. The aim of this study was to evaluate the place of the whole genome array comparative genomic hybridization method in pediatric cancers where difficulty is experienced in differential diagnosis.

methodIn Comparative Genomic Hybridization (CGH), 135,000 probes were scanned as 3 probes per gene in all genomes. It was possible to analyze paraffin block tissues obtained from the archive of the Pathology Laboratory of Dr. Behcet Uz Children's Hospital. DNA extraction was made from the paraffin blocks of 24 cases where difficulty had been experienced in making the differential diagnosis and in each case, comparisons with the control samples were made for all anomalies in all chromosomes using microarray technology.

resultsTogether with the typically observed chromosomal anomalies, additional derangements with debatable importance were determined.

conclusionThe whole genome CGH method may be useful in pediatric cancers where difficulties are experienced in making differential diagnoses. Since technical difficulties are experienced in the examination of paraffin-embedded tissue samples, storing fresh tissue samples from each tumor will be helpful for genetic and molecular examinations.

Indexed as

Comparative genomic hybridization (CGH)differential diagnosispediatric cancerssmall round cell malignant tumors

Identifiers

PMID31934157
PMCPMC6949692
OpenAlexW3005881373

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.