Evidence map›Paper›PMID 28515451›Full record

ArticleScientific reports2017

HOXA7, HOXA9, and HOXA10 are differentially expressed in clival and sacral chordomas.

Daniela Jäger, Thomas F E Barth, Silke Brüderlein, Angelika Scheuerle, Beate Rinner, Adrian von Witzleben, André Lechel, Patrick Meyer, Regine Mayer-Steinacker, Alexandra von Baer and 4 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.9field-weighted citation impact, top 10% 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

12 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Review
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  4. Article
  5. Molecular features and vulnerabilities of recurrent chordomas.Journal of experimental & clinical cancer research : CR · 2021
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  7. 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

14 authors at 2 institutions in 2 countries.

Daniela JägerInstitute of Pathology, University of Ulm, Ulm, Germany.
Thomas F E BarthInstitute of Pathology, University of Ulm, Ulm, Germany.
Silke BrüderleinInstitute of Pathology, University of Ulm, Ulm, Germany.
Angelika ScheuerleInstitute of Pathology, University of Ulm, Ulm, Germany.
Beate RinnerDivision of Biomedical Research, Medical University of Graz, Graz, Austria.
Adrian von WitzlebenInstitute of Pathology, University of Ulm, Ulm, Germany.
André LechelDepartment of Internal Medicine I, University of Ulm, Ulm, Germany.
Patrick MeyerDepartment of Dermatology, University of Ulm, Ulm, Germany.
Regine Mayer-SteinackerDepartment of Internal Medicine III, University of Ulm, Ulm, Germany.
Alexandra von BaerDepartment of Trauma Surgery, University of Ulm, Ulm, Germany.
Markus SchultheissDepartment of Trauma Surgery, University of Ulm, Ulm, Germany.
Christian R WirtzDepartment of Neurosurgery, University of Ulm, Ulm, Germany.
Peter MöllerInstitute of Pathology, University of Ulm, Ulm, Germany. peter.moeller@uniklinik-ulm.de.
Kevin MellertInstitute of Pathology, University of Ulm, Ulm, Germany.
Universität Ulm · DEMedical University of Graz · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chordomas are rare tumours of the bone arising along the spine from clivus to sacrum. We compared three chordoma cell lines of the clivus region including the newly established clivus chordoma cell line, U-CH14, with nine chordoma cell lines originating from sacral primaries by morphology, on genomic and expression levels and with patient samples from our chordoma tissue bank. Clinically, chordomas of the clivus were generally smaller in size at presentation and patients with sacral chordomas had more metastases and more often recurrent disease. All chordoma cell lines had a typical physaliphorous morphology and expressed brachyury, S100-protein and cytokeratin. By expression analyses we detected differentially expressed genes in the clivus derived cell lines as compared to the sacral cell lines. Among these were HOXA7, HOXA9, and HOXA10 known to be important for the development of the anterior-posterior body axis. These results were confirmed by qPCR. Immunohistologically, clivus chordomas had no or very low levels of HOXA10 protein while sacral chordomas showed a strong nuclear positivity in all samples analysed. This differential expression of HOX genes in chordomas of the clivus and sacrum suggests an oncofetal mechanism in gene regulation linked to the anatomic site.

Indexed as

Gene Expression Regulation, NeoplasticGenes, HomeoboxAdultAgedAged, 80 and overCell Line, TumorChordomaCranial Fossa, PosteriorFemaleGene Expression ProfilingHomeobox A10 ProteinsHomeodomain ProteinsHumansImmunohistochemistryMaleMiddle AgedHomeobox A10 Proteinshomeobox protein HOXA9Homeodomain ProteinsHOXA10 protein, humanHOXA7 protein, human

Identifiers

PMID28515451
PMCPMC5435709
OpenAlexW2612479016

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.