Evidence map›Paper›PMID 32867073›Full record

ArticleCancers2020

Cross-Species Proteomics Identifies CAPG and SBP1 as Crucial Invasiveness Biomarkers in Rat and Human Malignant Mesothelioma.

Joëlle S Nader, Alice Boissard, Cécile Henry, Isabelle Valo, Véronique Verrièle, Marc Grégoire, Olivier Coqueret, Catherine Guette, Daniel L Pouliquen

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.9field-weighted citation impact, top 11% 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

9 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
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  3. Signaling Network Response to α-Particle-Targeted Therapy with theJournal of nuclear medicine : official publication, Society of Nuclear Medicine · 2023
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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

9 authors at 1 institution in 1 country.

Joëlle S NaderUniversité de Nantes, Inserm, CRCINA, F-44000 Nantes, France.
Alice BoissardUniversité d'Angers, ICO Cancer Center, Inserm, CRCINA, F-44000 Nantes, France.
Cécile HenryUniversité d'Angers, ICO Cancer Center, Inserm, CRCINA, F-44000 Nantes, France.
Isabelle ValoUniversité d'Angers, ICO Cancer Center, Inserm, CRCINA, F-44000 Nantes, France.
Véronique VerrièleUniversité d'Angers, ICO Cancer Center, Inserm, CRCINA, F-44000 Nantes, France.
Marc GrégoireUniversité de Nantes, Inserm, CRCINA, F-44000 Nantes, France.
Olivier CoqueretUniversité d'Angers, Inserm, CRCINA, F-44000 Nantes, France.
Catherine GuetteUniversité d'Angers, ICO Cancer Center, Inserm, CRCINA, F-44000 Nantes, France.
Daniel L PouliquenUniversité d'Angers, Inserm, CRCINA, F-44000 Nantes, France.ORCID 0000-0002-0820-3828
Inserm · FR

Funding

Ligue Contre le Cancer R17029NN
6 · The paper itself

Abstract

Malignant mesothelioma (MM) still represents a devastating disease that is often detected too late, while the current effect of therapies on patient outcomes remains unsatisfactory. Invasiveness biomarkers may contribute to improving early diagnosis, prognosis, and treatment for patients, a task that could benefit from the development of high-throughput proteomics. To limit potential sources of bias when identifying such biomarkers, we conducted cross-species proteomic analyzes on three different MM sources. Data were collected firstly from two human MM cell lines, secondly from rat MM tumors of increasing invasiveness grown in immunocompetent rats and human MM tumors grown in immunodeficient mice, and thirdly from paraffin-embedded sections of patient MM tumors of the epithelioid and sarcomatoid subtypes. Our investigations identified three major invasiveness biomarkers common to the three tumor sources, CAPG, FABP4, and LAMB2, and an additional set of 25 candidate biomarkers shared by rat and patient tumors. Comparing the data to proteomic analyzes of preneoplastic and neoplastic rat mesothelial cell lines revealed the additional role of SBP1 in the carcinogenic process. These observations could provide new opportunities to identify highly vulnerable MM patients with poor survival outcomes, thereby improving the success of current and future therapeutic strategies.

Indexed as

biomarkerscarcinogenesisfatty acid-binding proteinlaminin subunit beta-2macrophage-capping proteinmalignant mesotheliomaproteomicsselenium-binding protein 1

Identifiers

PMID32867073
PMCPMC7564583
OpenAlexW3081448816

What Socratic 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 Socratic graph.