Evidence map›Paper›PMID 38784478›Full record

ArticleOncoscience2024

Targeting inflammatory factors for chemoprevention and cancer interception to tackle malignant mesothelioma.

Joseph R Testa, Yuwaraj Kadariya, Joseph S Friedberg

Abstract read
In one paragraph

Article in Oncoscience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–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.

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

1 citing paper in PubMed.

  1. 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

3 authors.

Joseph R TestaCancer Prevention and Control Program, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.
Yuwaraj KadariyaCancer Prevention and Control Program, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.
Joseph S FriedbergDepartment of Surgical Oncology, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.

Funding

CLC NIH HHS 75N90019D00022NIH HHS 75N99019D00022NIOSH CDC HHS U24 OH009077
6 · The paper itself

Abstract

Mesothelioma is an incurable cancer of the mesothelial lining often caused by exposure to asbestos. Asbestos-induced inflammation is a significant contributing factor in the development of mesothelioma, and genetic factors also play a role in the susceptibility to this rapidly progressive and treatment-resistant malignancy. Consequently, novel approaches are urgently needed to treat mesothelioma and prevent or reduce the overall incidence of this fatal disease. In this research perspective, we review the current state of chemoprevention and cancer interception progress in asbestos-induced mesothelioma. We discuss the different preclinical mouse models used for these investigations and the inflammatory factors that may be potential targets for mesothelioma prevention. Preliminary studies with naturally occurring phytochemicals and synthetic agents are reviewed. Results of previous clinical chemoprevention trials in populations exposed to asbestos and considerations regarding future trials are also presented.

Indexed as

asbestosBap1 mutationschemoprevention agentsinflammationpreclinical genetically engineered mouse models

Identifiers

PMID38784478
PMCPMC11115283

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.