Evidence map›Paper›PMID 24944814›Full record

ArticleBiomedical reports2014

Association between p16(CDKN2A) C540G polymorphism and tumor behavior in prolactinoma: A single-center study.

Soner Cander, Mutlu Karkucak, Ozen Oz Gul, Sebnem Ozemri Sag, Tahsin Yakut, Canan Ersoy, Ercan Tuncel, Erdinc Erturk

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In one paragraph

Article in Biomedical reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 38% 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

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
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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

8 authors at 1 institution in 1 country.

Soner CanderDepartment of Endocrinology and Metabolism, Uludag University Medical School, Gorukle, Bursa 16059, Turkey ; Department of Endocrinology and Metabolism, Sevket Yilmaz Education and Research Hospital, Osmangazi, Bursa 16230, Turkey.
Mutlu KarkucakDepartment of Medical Genetic, Uludag University Medical School, Gorukle, Bursa 16059, Turkey.
Ozen Oz GulDepartment of Endocrinology and Metabolism, Uludag University Medical School, Gorukle, Bursa 16059, Turkey.
Sebnem Ozemri SagDepartment of Medical Genetic, Uludag University Medical School, Gorukle, Bursa 16059, Turkey.
Tahsin YakutDepartment of Medical Genetic, Uludag University Medical School, Gorukle, Bursa 16059, Turkey.
Canan ErsoyDepartment of Endocrinology and Metabolism, Uludag University Medical School, Gorukle, Bursa 16059, Turkey.
Ercan TuncelDepartment of Endocrinology and Metabolism, Uludag University Medical School, Gorukle, Bursa 16059, Turkey.
Erdinc ErturkDepartment of Endocrinology and Metabolism, Uludag University Medical School, Gorukle, Bursa 16059, Turkey.
Bursa Uludağ Üni̇versi̇tesi̇ · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pituitary tumors usually originate as benign sporadic adenomas and develop into invasive and aggressive tumors such as prolactinomas, which are common functioning pituitary adenomas. The aim of the present study was to examine the association between the tumor behavior in prolactinomas and the p16(CDKN2A) gene polymorphism occurring at the 3'-untranslated region of exon 3 (C540G). A total of 104 patients with prolactinoma were included and assigned to two groups based on invasive vs. non-invasive tumor behavior. Ki67 indices were recorded according to histopathology results. Genotypic analysis of the p16(CDKN2A) C540G polymorphism was carried out using a modified polymerase chain reaction-restriction fragment length polymorphism assay. The corresponding frequencies for CC, CG and GG genotypes in non-invasive vs. invasive tumors were 61.5, 30.8, 7.7 and 64.1, 28.2, 7.7%, respectively (not significant). The observed CG genotype frequency was higher compared with previous studies. In addition, the patients with giant adenomas or a high Ki67 index had a higher frequency of the CG genotype as compared with the other subgroups, although the differences were not significant (46.2 and 42.9%, respectively). In conclusion, a higher frequency of the C540G CG genotype of the CDKN2A gene was found among patients with prolactinoma in comparison with previous studies. These frequencies were also higher in the subgroups with elevated Ki67 or giant adenomas. Further studies are required to improve the definition of the role of the CG genotype in the development and progression of tumors in prolactinomas.

Indexed as

CDKN2A C540G polymorphisminvasivenessprolactinomatumor behavior

Identifiers

PMID24944814
PMCPMC4051468
OpenAlexW2145713110

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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.