Evidence map›Paper›PMID 28191281›Full record

ReviewGenes & cancer2016

Switching off malignant mesothelioma: exploiting the hypoxic microenvironment.

Noushin Nabavi, Kevin L Bennewith, Andrew Churg, Yuzhuo Wang, Colin C Collins, Luciano Mutti

Open access · diamondAbstract readReview
In one paragraph

Review in Genes & cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.9field-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

14 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. The effect of CELLFOODTherapeutic advances in medical oncology · 2019
    Article
  11. Review
  12. Article
  13. Scientific Advances and New Frontiers in Mesothelioma Therapeutics.Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer · 2018
    Review
  14. 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
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

6 authors at 4 institutions in 2 countries.

Noushin NabaviLaboratory for Advanced Genome Analysis, Vancouver Prostate Centre, BC, Canada; Department of Urologic Sciences, University of British Columbia, BC, Canada; Department of Experimental Therapeutics, BC Cancer Agency, BC, Canada.
Kevin L BennewithDepartment of Integrative Oncology, BC Cancer Agency, BC, Canada; Department of Pathology and Laboratory Medicine, University of British Columbia, BC, Canada.
Andrew ChurgDepartment of Pathology and Laboratory Medicine, University of British Columbia, BC, Canada.
Yuzhuo WangDepartment of Urologic Sciences, University of British Columbia, BC, Canada; Department of Experimental Therapeutics, BC Cancer Agency, BC, Canada.
Colin C CollinsLaboratory for Advanced Genome Analysis, Vancouver Prostate Centre, BC, Canada; Department of Urologic Sciences, University of British Columbia, BC, Canada.
Luciano MuttiItalian Group for Research and Therapy for Mesothelioma (GIMe) & School of Environment and Life Sciences, University of Salford, Manchester, United Kingdom.
BC Cancer Agency · CAGenome British Columbia · CAUniversity of British Columbia · CAUniversity of Salford · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Malignant mesotheliomas are aggressive, asbestos-related cancers with poor patient prognosis, typically arising in the mesothelial surfaces of tissues in pleural and peritoneal cavity. The relative unspecific symptoms of mesotheliomas, misdiagnoses, and lack of precise targeted therapies call for a more critical assessment of this disease. In the present review, we categorize commonly identified genomic aberrations of mesotheliomas into their canonical pathways and discuss targeting these pathways in the context of tumor hypoxia, a hallmark of cancer known to render solid tumors more resistant to radiation and most chemo-therapy. We then explore the concept that the intrinsic hypoxic microenvironment of mesotheliomas can be Achilles' heel for targeted, multimodal therapeutic intervention.

Indexed as

angiogenesiscell cycleDNA damagehypoxiamesotheliomametabolismproteolysissolid tumors

Identifiers

PMID28191281
PMCPMC5302036
OpenAlexW2795512548

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.