Evidence map›Paper›PMID 25757056›Full record

ArticleJournal of cellular biochemistry2015

Differential Susceptibility of Human Pleural and Peritoneal Mesothelial Cells to Asbestos Exposure.

Julie Dragon, Joyce Thompson, Maximilian MacPherson, Arti Shukla

Open access · greenAbstract read
In one paragraph

Article in Journal of cellular biochemistry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

18 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. New insights in the pathology of peritoneal surface malignancy.Journal of gastrointestinal oncology · 2021
    Review
  9. Normal mesothelial cell lines newly derived from human pleural biopsy explants.American journal of physiology. Lung cellular and molecular physiology · 2020
    Article
  10. Article
  11. Health impact of exposure to asbestos in polluted area of Southern Italy.Journal of preventive medicine and hygiene · 2019
    Review
  12. Article
  13. Exosomes from asbestos-exposed cells modulate gene expression in mesothelial cells.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2018
    Article
  14. Review
  15. Translational lung cancer research · 2017
    Review
  16. Article
  17. Review
  18. 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

4 authors at 1 institution in 1 country.

Julie DragonDepartment of Microbiology and Molecular Genetics, College of Medicine, University of Vermont, Burlington, Vermont, 05405.
Joyce ThompsonDepartment of Pathology and Laboratory Medicine, College of Medicine, University of Vermont, Burlington, Vermont, 05405.
Maximilian MacPhersonDepartment of Pathology and Laboratory Medicine, College of Medicine, University of Vermont, Burlington, Vermont, 05405.
Arti ShuklaDepartment of Pathology and Laboratory Medicine, College of Medicine, University of Vermont, Burlington, Vermont, 05405.
University of Vermont · US

Funding

Vermont INBRE Administrative Supplement 2024 AWD 118P20GM103449 · NIGMS · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI CHRISTOPHER S FRANCKLYN · 2012 to 2026
$58.4M
Inflammasomes in pathogenesis of mesotheliomaR01ES021110 · NIEHS · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI SHUKLA, ARTI · 2012 to 2016
$1.7M
NIEHS NIH HHS R01 ES021110NIGMS NIH HHS P20 GM103449
6 · The paper itself

Abstract

Malignant mesothelioma (MM) is an aggressive cancer of mesothelial cells of pleural and peritoneal cavities. In 85% of cases both pleural and peritoneal MM is caused by asbestos exposure. Although both are asbestos-induced cancers, the incidence of pleural MM is significantly higher (85%) than peritoneal MM (15%). It has been proposed that carcinogenesis is a result of asbestos-induced inflammation but it is not clear what contributes to the differences observed between incidences of these two cancers. We hypothesize that the observed differences in incidences of pleural and peritoneal MM are the result of differences in the direct response of these cell types to asbestos rather than to differences mediated by the in vivo microenvironment. To test this hypothesis we characterized cellular responses to asbestos in a controlled environment. We found significantly greater changes in genome-wide expression in response to asbestos exposure in pleural mesothelial cells as compared to peritoneal mesothelial cells. In particular, a greater response in many common genes (IL-8, ATF3, CXCL2, CXCL3, IL-6, GOS2) was seen in pleural mesothelial cells as compared to peritoneal mesothelial cells. Unique genes expressed in pleural mesothelial cells were mainly pro-inflammatory (G-CSF, IL-1β, IL-1α, GREM1) and have previously been shown to be involved in development of MM. Our results are consistent with the hypothesis that differences in incidences of pleural and peritoneal MM upon exposure to asbestos are the result of differences in mesothelial cell physiology that lead to differences in the inflammatory response, which leads to cancer.

Indexed as

AdultAgedAsbestos, CrocidoliteCell LineCell SurvivalFemaleGene Expression Regulation, NeoplasticGenetic Predisposition to DiseaseHigh-Throughput Nucleotide SequencingHumansInflammationLung NeoplasmsMaleMesotheliomaMesothelioma, MalignantMiddle AgedAsbestos, CrocidoliteASBESTOSINFLAMMATIONMASSIVELY PARALLEL SEQUENCINGMESOTHELIAL CELLSMESOTHELIOMARNA-SEQ

Identifiers

PMID25757056
PMCPMC4698803
OpenAlexW2157574237

What OpenQuestion holds

Textmetadata
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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.