Evidence map›Paper›PMID 27072875›Full record

ArticleScientific reports2016

Establishment of clival chordoma cell line MUG-CC1 and lymphoblastoid cells as a model for potential new treatment strategies.

Verena Gellner, Peter Valentin Tomazic, Birgit Lohberger, Katharina Meditz, Ellen Heitzer, Michael Mokry, Wolfgang Koele, Andreas Leithner, Bernadette Liegl-Atzwanger, Beate Rinner

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. 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
2.4field-weighted citation impact, top 13% 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, 17 citations in OpenAlex.

  1. Article
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  6. Review
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  8. Article
  9. In focus in HCB.Histochemistry and cell biology · 2018
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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

10 authors at 1 institution in 1 country.

Verena GellnerDepartment of Neurosurgery, Medical University of Graz, 8036 Graz, Austria.
Peter Valentin TomazicDepartment of General Otorhinolaryngology, Head and Neck Surgery, Medical University of Graz, 8036 Graz, Austria.
Birgit LohbergerDepartment of Orthopedic Surgery, Medical University of Graz, 8036 Graz, Austria.
Katharina MeditzDivision of Biomedical Research, Medical University of Graz, 8036 Graz, Austria.
Ellen HeitzerInstitute of Human Genetics, Medical University of Graz, 8036 Graz, Austria.
Michael MokryDepartment of Neurosurgery, Medical University of Graz, 8036 Graz, Austria.
Wolfgang KoeleDepartment of Neurosurgery, Medical University of Graz, 8036 Graz, Austria.
Andreas LeithnerDepartment of Orthopedic Surgery, Medical University of Graz, 8036 Graz, Austria.
Bernadette Liegl-AtzwangerInstitute of Pathology, Medical University of Graz, 8036 Graz, Austria.
Beate RinnerDivision of Biomedical Research, Medical University of Graz, 8036 Graz, Austria.
Medical University of Graz · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chordomas are rare malignant tumors that develop from embryonic remnants of the notochord and arise only in the midline from the clivus to the sacrum. Surgery followed by radiotherapy is the standard treatment. As chordomas are resistant to standard chemotherapy, further treatment options are urgently needed. We describe the establishment of a clivus chordoma cell line, MUG-CC1. The cell line is characterized according to its morphology, immunohistochemistry, and growth kinetics. During establishment, cell culture supernatants were collected, and the growth factors HGF, SDF-1, FGF2, and PDGF analyzed using xMAP(®) technology. A spontaneous lymphoblastoid EBV-positive cell line was also developed and characterized. MUG-CC1 is strongly positive for brachyury, cytokeratin, and S100. The cell line showed gains of the entire chromosomes 7, 8, 12, 13, 16, 18, and 20, and high level gains on chromosomes 1q21-1q24 and 17q21-17q25. During cultivation, there was significant expression of HGF and SDF-1 compared to continuous chordoma cell lines. A new, well-characterized clival chordoma cell line, as well as a non-tumorigenic lymphoblastoid cell line should serve as an in vitro model for the development of potential new treatment strategies for patients suffering from this disease.

Indexed as

AgedBrachyury ProteinCell Culture TechniquesCell Line, TumorCell ProliferationCells, CulturedChordomaChromosomes, Human, Pair 1Chromosomes, Human, Pair 17Fetal ProteinsHumansIntercellular Signaling Peptides and ProteinsKeratinsLymphocytesMaleS100 ProteinsBrachyury ProteinFetal ProteinsIntercellular Signaling Peptides and ProteinsKeratinsS100 ProteinsT-Box Domain Proteins

Identifiers

PMID27072875
PMCPMC4829844
OpenAlexW2340020353

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 OpenQuestion graph.