Evidence map›Paper›PMID 29404144›Full record

ArticleTurkish thoracic journal2016

Analysis of Chromosome 3, 7 and 8 Centromeric Regions in Bronchial Lavage Specimens by FISH.

Sezen Atasoy, Salih Serdar Erturan, Nail Yılmaz, Dilhan Kuru, Ayşe Çırakoğlu, Şükriye Yılmaz, Ayhan Deviren

Abstract read
In one paragraph

Article in Turkish thoracic journal, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact, top 100% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
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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

7 authors at 1 institution in 1 country.

Sezen AtasoyDepartment of Medical Biology, İstanbul University Cerrahpaşa Faculty of Medicine, İstanbul, Turkey.
Salih Serdar ErturanDepartment of Chest Diseases, İstanbul University Cerrahpaşa Faculty of Medicine, İstanbul, Turkey.
Nail YılmazDepartment of Chest Diseases, İstanbul University Cerrahpaşa Faculty of Medicine, İstanbul, Turkey.
Dilhan KuruDepartment of Medical Biology, İstanbul University Cerrahpaşa Faculty of Medicine, İstanbul, Turkey.
Ayşe ÇırakoğluDepartment of Medical Biology, İstanbul University Cerrahpaşa Faculty of Medicine, İstanbul, Turkey.
Şükriye YılmazDepartment of Medical Biology, İstanbul University Cerrahpaşa Faculty of Medicine, İstanbul, Turkey.
Ayhan DevirenDepartment of Medical Biology, İstanbul University Cerrahpaşa Faculty of Medicine, İstanbul, Turkey.
Istanbul University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesMultiple genetic changes are observed in malignant tumors but are rare or absent in benign conditions. Aneuploidy is the most common feature of solid tumors including lung cancer and diagnosis of malignant tumors is possible through detection of aneuploidy. The aim of this study was to investigate chromosomal abnormalities in cells from non-small cell lung cancer patients obtained bronchoscopically and to evaluate the suitability of fluorescence in situ hybridization (FISH). MATERIAL AND

methodsBronchial lavage samples of 17 non-small cell lung cancer (NSCLC) patients were evaluated with four-color FISH using deoxyribonucleic acid (DNA) probes specific for the centromere regions of chromosomes 3, 7 and 8. tested specimens were first hybridized with probes, then visualized under fluorescence microscobe and captured with device's camera.

resultsHigh number of aneuploidic cells were detected in all the samples. Increased or decreased abnormal copies or chromosomes 3, 7 and 8 were obserced in all the 17 patients. Aneuploidy of chromosome 3 (21.35%) was higher than those of chromosome 7 (9.06%) and chromosome 8 (15.47%). Moreover, our results were significant for monosomy and trisomy of chromosome 3, trisomy of chromosome 7, nullisomy, monosomy and trisomy of, chromosome 8 (p< 0.05).

conclusionIt has been observed that FISH is a useful technique for detection of aneuploidy in bronchial lavage samples obtained by bronchoscopy. Interphase cells were evaluated without cell culturing with this method and high number of tumor cells were enumerated rapidly. Our study has demonstrated that, FISH technique may be used successfully in detection of chromosome number abnormalities in NSCLC patients and may facilitate evaluation of genetic abnormalities.

Indexed as

aneuploidybronchial lavagecytogeneticfluorescence in situ hybridizationLung cancer

Identifiers

PMID29404144
PMCPMC5783093
OpenAlexW2565395660

What Socratic holds

Textmetadata
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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 Socratic graph.