Evidence map›Paper›PMID 10954737›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2000

Human mesothelial cells are unusually susceptible to simian virus 40-mediated transformation and asbestos cocarcinogenicity.

M Bocchetta, I Di Resta, A Powers, R Fresco, A Tosolini, J R Testa, H I Pass, P Rizzo, M Carbone

Registry-linked trialAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01590472 (Consortium for the Sharing of Germ Line DNA and Tissue From Subjects With Mesothelioma), which is not on this map. Cited by 88 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
88citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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.

NCT01590472 completednot on this mapstarted 2011, after this paper: background citation

Consortium for the Sharing of Germ Line DNA and Tissue From Subjects With Mesothelioma

TypeobservationalSponsorWake Forest UniversityRan2011 to 2015Enrolled69ConditionsMesothelioma
3 · Its place in the literature

Who cites it

88 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Radiotherapy for malignant pleural mesothelioma.The Cochrane database of systematic reviews · 2006
    Pooled it
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. BAP1 forms a trimer with HMGB1 and HDAC1 that modulates gene × environment interaction with asbestos.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  10. Article
  11. Update on biology and management of mesothelioma.European respiratory review : an official journal of the European Respiratory Society · 2021
    Review
  12. Normal mesothelial cell lines newly derived from human pleural biopsy explants.American journal of physiology. Lung cellular and molecular physiology · 2020
    Article
  13. Article
  14. SV40 and human mesothelioma.Translational lung cancer research · 2020
    Review
  15. Article
  16. Review
  17. Review
  18. Article
  19. The oncogenic neurotrophin receptor tropomyosin-related kinase variant, TrkAIII.Journal of experimental & clinical cancer research : CR · 2018
    Review
  20. Review

28 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

M BocchettaCancer Immunology Program, Department of Pathology, Cardinal Bernardin Cancer Center, Loyola University Chicago, Maywood, IL 60153, USA.
I Di Resta
A Powers
R Fresco
A Tosolini
J R Testa
H I Pass
P Rizzo
M Carbone

Funding

SV40-LIKE SEQUENCES IN HUMAN TUMORS ANALYSESR29CA077220 · NCI · LOYOLA UNIVERSITY CHICAGO · PI CARBONE, MICHELE · 1997 to 2001
$217k
NCI NIH HHS CA-77220-1
6 · The paper itself

Abstract

Mesothelioma, a malignancy associated with asbestos, has been recently linked to simian virus 40 (SV40). We found that infection of human mesothelial cells by SV40 is very different from the semipermissive infection thought to be characteristic of human cells. Mesothelial cells are uniformly infected but not lysed by SV40, a mechanism related to p53, and undergo cell transformation at an extremely high rate. Exposure of mesothelial cells to asbestos complemented SV40 mutants in transformation. Our data provide a mechanistic explanation for the ability of SV40 to transform mesothelial cells preferentially and indicate that asbestos and SV40 may be cocarcinogens.

Indexed as

Cell Transformation, NeoplasticSimian virus 40AsbestosCarcinogensCells, CulturedEpithelial CellsFibroblastsHumansMesotheliomaTumor Suppressor Protein p53AsbestosCarcinogensTumor Suppressor Protein p53

Identifiers

PMID10954737
PMCPMC27818

What OpenQuestion holds

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Read underepoch 390

Registered trials

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.