Evidence map›Paper›PMID 37626858›Full record

ReviewCells2023

Chronic Inflammation, Oxidative Stress and Metabolic Plasticity: Three Players Driving the Pro-Tumorigenic Microenvironment in Malignant Mesothelioma.

Irene Fiorilla, Simona Martinotti, Alberto Maria Todesco, Gregorio Bonsignore, Maria Cavaletto, Mauro Patrone, Elia Ranzato, Valentina Audrito

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
7.0field-weighted citation impact, top 2% 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

22 citing papers in PubMed, 27 citations in OpenAlex.

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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

8 authors at 1 institution in 1 country.

Irene FiorillaDepartment of Science and Technological Innovation (DISIT), University of Eastern Piedmont, 15121 Alessandria, Italy.
Simona MartinottiDepartment of Science and Technological Innovation (DISIT), University of Eastern Piedmont, 15121 Alessandria, Italy.ORCID 0000-0003-2891-1810
Alberto Maria TodescoDepartment of Science and Technological Innovation (DISIT), University of Eastern Piedmont, 15121 Alessandria, Italy.
Gregorio BonsignoreDepartment of Science and Technological Innovation (DISIT), University of Eastern Piedmont, 15121 Alessandria, Italy.ORCID 0000-0003-0225-5763
Maria CavalettoDepartment for Sustainable Development and Ecological Transition (DISSTE), University of Eastern Piedmont, 13100 Vercelli, Italy.ORCID 0000-0002-8511-161X
Mauro PatroneDepartment of Science and Technological Innovation (DISIT), University of Eastern Piedmont, 15121 Alessandria, Italy.ORCID 0000-0002-7740-2396
Elia RanzatoDepartment of Science and Technological Innovation (DISIT), University of Eastern Piedmont, 15121 Alessandria, Italy.ORCID 0000-0002-7600-8215
Valentina AudritoDepartment of Science and Technological Innovation (DISIT), University of Eastern Piedmont, 15121 Alessandria, Italy.ORCID 0000-0002-5660-4175
Università degli Studi del Piemonte Orientale “Amedeo Avogadro” · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Malignant pleural mesothelioma (MPM) is a lethal and rare cancer, even if its incidence has continuously increased all over the world. Asbestos exposure leads to the development of mesothelioma through multiple mechanisms, including chronic inflammation, oxidative stress with reactive oxygen species (ROS) generation, and persistent aberrant signaling. Together, these processes, over the years, force normal mesothelial cells' transformation. Chronic inflammation supported by "frustrated" macrophages exposed to asbestos fibers is also boosted by the release of pro-inflammatory cytokines, chemokines, growth factors, damage-associated molecular proteins (DAMPs), and the generation of ROS. In addition, the hypoxic microenvironment influences MPM and immune cells' features, leading to a significant rewiring of metabolism and phenotypic plasticity, thereby supporting tumor aggressiveness and modulating infiltrating immune cell responses. This review provides an overview of the complex tumor-host interactions within the MPM tumor microenvironment at different levels, i.e., soluble factors, metabolic crosstalk, and oxidative stress, and explains how these players supporting tumor transformation and progression may become potential and novel therapeutic targets in MPM.

Indexed as

Mesothelioma, MalignantCarcinogenesisHumansInflammationOxidative StressReactive Oxygen SpeciesTumor MicroenvironmentReactive Oxygen SpeciesDAMPinflammationmacrophagesmesotheliomametabolic adaptationoxidative stressphenotype plasticitytumor microenvironment

Identifiers

PMID37626858
PMCPMC10453755
OpenAlexW4385759859

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.