Evidence map›Paper›PMID 30734484›Full record

ArticleThoracic cancer2019

Alteration in gene expression profile of thymomas with or without myasthenia gravis linked with the nuclear factor-kappaB/autoimmune regulator pathway to myasthenia gravis pathogenesis.

Feng Guo, Chun-Yang Wang, Shuo Wang, Jun Zhang, Yi-Jie Yan, Zhi-Yu Guan, Fan-Jie Meng

Open access · goldAbstract read
In one paragraph

Article in Thoracic cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

6 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
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  5. Narrative review of immunotherapy in thymic malignancies.Translational lung cancer research · 2021
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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

7 authors at 3 institutions in 1 country.

Feng GuoDepartment of Endoscopy, Key Laboratory of Cancer Prevention and Therapy, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Tianjin's Clinical Research Center for Cancer, Tianjin, China.
Chun-Yang WangDepartment of Neurology, Tianjin Medical University General Hospital, Tianjin, China.
Shuo WangDepartment of Thoracic Surgery, The Second Hospital of Tianjin Medical University, Tianjin, China.
Jun ZhangDepartment of Thoracic Surgery, The Second Hospital of Tianjin Medical University, Tianjin, China.
Yi-Jie YanDepartment of Thoracic Surgery, The Second Hospital of Tianjin Medical University, Tianjin, China.
Zhi-Yu GuanDepartment of Thoracic Surgery, The Second Hospital of Tianjin Medical University, Tianjin, China.
Fan-Jie MengDepartment of Thoracic Surgery, The Second Hospital of Tianjin Medical University, Tianjin, China.ORCID 0000-0002-0783-1961
Second Hospital of Tianjin Medical University · CNTianjin Medical University Cancer Institute and Hospital · CNTianjin Medical University General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTo investigate the gene expression profile of a set of candidate genes for a better understanding of the molecular mechanism underlying the pathogenesis of thymoma with or without myasthenia gravis.

methodsThymoma patients and thymoma patients with myasthenia gravis were analyzed using microarray profiling to identify significant changes in gene expression of autoimmune regulator pathway genes including AIRE, IL-7R, CHRNA3, SYMD1, THRA, and CAV3.

resultsAcross all of our samples, we found that 1484 mRNAs were upregulated and 770 were downregulated in thymoma patients compared with thymoma with myasthenia gravis patients. Gene ontology and pathway analysis revealed that a large number of genes participated in cellular functions for humoral immune response, sequence-specific DNA binding RNA polymerase II transcription factor activity, positive regulation of gene expression, regulation of neuron projection development, extracellular ligand-gated ion channel activity, positive regulation of striated muscle cell differentiation, and regulation of nuclear factor-kappaB import into the nucleus.

conclusionOur results revealed genetic differences between thymomas and myasthenia gravis, and identified the key candidate genes/pathways for molecular mechanism.

Indexed as

AdultAIRE ProteinAutoimmune DiseasesCaveolin 3FemaleGene Expression Regulation, NeoplasticHumansMaleMicroarray AnalysisMiddle AgedMyasthenia GravisNeoplasm ProteinsNF-kappa BReceptors, Interleukin-7Receptors, NicotinicThymomaAIRE ProteinCAV3 protein, humanCaveolin 3Neoplasm ProteinsNF-kappa BReceptors, Interleukin-7Receptors, NicotinicThyroid Hormone Receptors alphaTranscription FactorsAnalysisgene ontologymicroarraymyasthenia gravispathwaythymoma

Identifiers

PMID30734484
PMCPMC6397909
OpenAlexW2912721331

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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.