Evidence map›Paper›PMID 32373124›Full record

ArticleFrontiers in immunology2020

Thymoma Associated Myasthenia Gravis (TAMG): Differential Expression of Functional Pathways in Relation to MG Status in Different Thymoma Histotypes.

Yosuke Yamada, Cleo-Aron Weis, Julian Thelen, Carsten Sticht, Berthold Schalke, Philipp Ströbel, Alexander Marx

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.1field-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

20 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Myasthenia gravis: the future is here.The Journal of clinical investigation · 2024
    Review
  5. Article
  6. The Molecular Landscape of Thymic Epithelial Tumors: A Comprehensive Review.International journal of molecular sciences · 2024
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Molecular pathology of thymomas: implications for diagnosis and therapy.Virchows Archiv : an international journal of pathology · 2021
    Review
  20. Article
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 4 institutions in 1 country.

Yosuke YamadaInstitute of Pathology, University Medical Centre Mannheim, Heidelberg University, Mannheim, Germany.
Cleo-Aron WeisInstitute of Pathology, University Medical Centre Mannheim, Heidelberg University, Mannheim, Germany.
Julian ThelenInstitute of Pathology, University Medical Centre Mannheim, Heidelberg University, Mannheim, Germany.
Carsten StichtMedical Faculty Mannheim, Medical Research Center, Heidelberg University, Mannheim, Germany.
Berthold SchalkeDepartment of Neurology, University of Regensburg, Regensburg, Germany.
Philipp StröbelInstitute of Pathology, University Medical Center Göttingen, University of Göttingen, Göttingen, Germany.
Alexander MarxInstitute of Pathology, University Medical Centre Mannheim, Heidelberg University, Mannheim, Germany.
Heidelberg University · DEUniversity Medical Centre Mannheim · DEUniversity of Göttingen · DEUniversity of Regensburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A unique feature of thymomas is their unrivaled frequency of associated myasthenia gravis (MG). Previous studies reported that MG+ thymomas contain a larger number of mature "pre-emigrant" CD4+ T cells than MG- thymomas and that most thymomas do not contain AIRE expressing cells irrespective of MG status. These findings suggest that CD4+ T cells that mature inside the abnormal microenvironment of thymomas and egress to the blood are critical to the development of thymoma-associated MG (TAMG) irrespective of thymoma histotype. However, underlying mechanisms have remained enigmatic. To get hints to mechanisms underlying TAMG, we pursue three hypotheses: (i) Functional pathways with metabolic and immunological relevance might be differentially expressed in TAMG(+) compared to TAMG(-) thymomas; (ii) differentially enriched pathways might be more evident in immature lymphocyte-poor (i.e., tumor cell/stroma-rich) thymoma subgroups; and (iii) mechanisms leading to TAMG might be different among thymoma histological subtypes. To test these hypotheses, we compared the expression of functional pathways with potential immunological relevance (

Indexed as

CarcinogenesisCell DifferentiationDatasets as TopicEpithelial CellsGene Expression Regulation, NeoplasticHumansLymphocytesMacrophagesMyasthenia GravisSignal TransductionThymomaThymus GlandThymus NeoplasmsTranscriptomeTumor Microenvironmentautoimmunityfunctional pathwaysmacrophage polarizationmetabolismmyasthenia gravisthe cancer genome atlas (TCGA)thymoma

Identifiers

PMID32373124
PMCPMC7176899
OpenAlexW3016364291

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.