Evidence map›Paper›PMID 22161024›Full record

ArticlePathology oncology research : POR2012

Amplification of thymosin beta 10 and AKAP13 genes in metastatic and aggressive papillary thyroid carcinomas.

Liliána Z Fehér, Gábor Pocsay, László Krenács, Agnes Zvara, Enikő Bagdi, Réka Pocsay, Géza Lukács, Ferenc Győry, Andrea Gazdag, Erzsébet Tarkó and 1 more

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Article in Pathology oncology research : POR, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 16% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

  1. Pooled it
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  9. Identification of RAB2A and PRDX1 as the potential biomarkers for oral squamous cell carcinoma using mass spectrometry-based comparative proteomic approach.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2015
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  13. [Thymosin beta 10 prompted the VEGF-C expression in lung cancer cell].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2014
    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

11 authors at 4 institutions in 1 country.

Liliána Z FehérLaboratory of Functional Genomics, Biological Research Centre, Hungarian Academy of Sciences, P.O. Box 521, Szeged, 6701, Hungary.
Gábor Pocsay
László Krenács
Agnes Zvara
Enikő Bagdi
Réka Pocsay
Géza Lukács
Ferenc Győry
Andrea Gazdag
Erzsébet Tarkó
László G Puskás
Békés Megyei Központi Kórház · HUHUN-REN Szegedi Biológiai Kutatóközpont · HUUniversity of Debrecen · HUBorsod-Abaúj-Zemplén Megyei Kórház és Egyetemi Oktató Kórház · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Papillary thyroid carcinoma (PTC) is the most common well-differentiated thyroid cancer. Although the great majority of the cases exhibit an indolent clinical course, some of them develop local invasion with distant metastasis, and a few cases transform into undifferentiated/anaplastic thyroid carcinoma with a rapidly lethal course. To identify gene copy number alterations predictive of metastatic potential or aggressive transformation, array-based comparative genomic hybridization (CGH-array) was performed in 43 PTC cases. Formalin-fixed and paraffin-embedded samples from primary tumours of 16 cases without metastasis, 14 cases with only regional lymph node metastasis, and 13 cases with distant metastasis, recurrence or extrathyroid extension were analysed. The CGH-array and confirmatory quantitative real-time PCR results identified the deletion of the EIF4EBP3 and TRAK2 gene loci, while amplification of thymosin beta 10 (TB10) and Tre-2 oncogene regions were observed as general markers for PTC. Although there have been several studies implicating TB10 as a specific marker based on gene expression data, our study is the first to report on genomic amplification. Although no significant difference could be detected between the good and bad prognosis cases in the A-kinase anchor protein 13 (AKAP13) gene region, it was discriminative markers for metastasis. Amplification in the AKAP13 region was demonstrated in 42.9% and 15.4% of the cases with local or with distant metastasis, respectively, while no amplification was detected in non-metastatic cases. AKAP13 and TB10 regions may represent potential new genomic markers for PTC and cancer progression.

Indexed as

Gene AmplificationAdolescentAdultAgedA Kinase Anchor ProteinsBiomarkers, TumorBone NeoplasmsCarcinoma, PapillaryComparative Genomic HybridizationDNA, NeoplasmFemaleFollow-Up StudiesGene DosageGene Expression Regulation, NeoplasticHumansImmunoenzyme TechniquesAKAP13 protein, humanA Kinase Anchor ProteinsBiomarkers, TumorDNA, NeoplasmMinor Histocompatibility AntigensProto-Oncogene ProteinsThymosinthymosin beta(10)

Identifiers

PMID22161024
OpenAlexW2057760066

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.