Evidence map›Paper›PMID 16795078›Full record

ReviewJournal of cellular biochemistry2006

Cellular and molecular parameters of mesothelioma.

Maria E Ramos-Nino, Joseph R Testa, Deborah A Altomare, Harvey I Pass, Michele Carbone, Maurizio Bocchetta, Brooke T Mossman

Open access · greenAbstract readReview
In one paragraph

Review in Journal of cellular biochemistry, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
6.8field-weighted citation impact, top 3% 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

31 citing papers in PubMed, 70 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Malignant pleural mesothelioma: an update.Jornal brasileiro de pneumologia : publicacao oficial da Sociedade Brasileira de Pneumologia e Tisilogia · 2021
    Review
  7. Live-cell imaging of macrophage phagocytosis of asbestos fibers under fluorescence microscopy.Genes and environment : the official journal of the Japanese Environmental Mutagen Society · 2019
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  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.

Maria E Ramos-NinoDepartment of Pathology, University of Vermont College of Medicine, Burlington, Vermont 05405, USA. Maria.Ramos@uvm.edu
Joseph R Testa
Deborah A Altomare
Harvey I Pass
Michele Carbone
Maurizio Bocchetta
Brooke T Mossman
Fox Chase Cancer Center · USLoyola University Chicago · USUniversity of Vermont · USNew York University · US

Funding

PATHOLOGY, VIROLOGY, AND ANIMAL COREP01CA114047 · NCI · UNIVERSITY OF HAWAII AT MANOA · PI CARBONE, MICHELE · 2006 to 2010
$8.0M
MOLECULAR GENETIC ALTERATIONS IN MALIGNANT MESOTHELIOMAR01CA045745 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI TESTA, JOSEPH R. · 1987 to 2006
$1.8M
Role of Cell Mediators in Asbestos-SV40 CarcinogenesisR01CA106567 · NCI · UNIVERSITY OF HAWAII AT MANOA · PI CARBONE, MICHELE · 2005 to 2009
$1.3M
Role of Fra-1 in MesotheliomaK01CA104159 · NCI · UNIVERSITY OF VERMONT &ST AGRIC COLLEGE · PI RAMOS-NINO, MARIA E · 2004 to 2008
$631k
NCI NIH HHS CA45745NCI NIH HHS K01 CA104159NCI NIH HHS K01CA104159-01NCI NIH HHS P01 CA114047NCI NIH HHS R01 CA045745NCI NIH HHS R01CA082657-01NCI NIH HHS R01CA10656NCI NIH HHS R01 CA106567
6 · The paper itself

Abstract

Malignant mesotheliomas (MM) are neoplasms arising from mesothelial cells that line the body cavities, most commonly the pleural and peritoneal cavities. Although traditionally recognized as associated with occupational asbestos exposures, MMs can appear in individuals with no documented exposures to asbestos fibers, and emerging data suggest that genetic susceptibility and simian virus 40 (SV40) infections also facilitate the development of MMs. Both asbestos exposure and transfection of human mesothelial cells with SV40 large and small antigens (Tag, tag) cause genetic modifications and cell signaling events, most notably the induction of cell survival pathways and activation of receptors, and other proteins that favor the growth and establishment of MMs as well as their resistance to chemotherapy. Recent advances in high-throughput technologies documenting gene and protein expression in patients and animal models of MMs can now be validated in human MM tissue arrays. These have revealed expression profiles that allow more accurate diagnosis and prognosis of MMs. More importantly, serum proteomics has revealed two new candidates (osteopontin and serum mesothelin-related protein or SMRP) potentially useful in screening individuals for MMs. These mechanistic approaches offer new hope for early detection and treatment of these devastating tumors.

Indexed as

Cell Transformation, ViralSimian virus 40AnimalsAsbestosCell Transformation, NeoplasticHumansMesotheliomaPeritoneal NeoplasmsPleural NeoplasmsPolyomavirus InfectionsTumor Virus InfectionsAsbestos

Identifiers

PMID16795078
PMCPMC2766267
OpenAlexW2057869668

What OpenQuestion holds

Textmetadata
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.