Evidence map›Paper›PMID 35832452›Full record

ArticleTranslational lung cancer research2022

Malignant pleural mesothelioma nodules remodel their surroundings to vascularize and grow.

Ildiko Kovacs, Edina Bugyik, Katalin Dezso, Julia Tarnoki-Zach, Elod Mehes, Marton Gulyas, Andras Czirok, Elisabeth Lang, Michael Grusch, Karin Schelch and 12 more

Open access · diamondAbstract read
In one paragraph

Article in Translational lung cancer research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 42% 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

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
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

22 authors at 7 institutions in 4 countries.

Ildiko KovacsNational Koranyi Institute of Pulmonology, Budapest, Hungary.
Edina BugyikNational Koranyi Institute of Pulmonology, Budapest, Hungary.
Katalin Dezso1st Department of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary.
Julia Tarnoki-ZachDepartment of Biological Physics, Eotvos University, Budapest, Hungary.
Elod MehesNational Koranyi Institute of Pulmonology, Budapest, Hungary.
Marton GulyasDepartment of Biological Physics, Eotvos University, Budapest, Hungary.
Andras CzirokDepartment of Biological Physics, Eotvos University, Budapest, Hungary.
Elisabeth LangInstitute of Cancer Research, Department of Medicine I, Medical University of Vienna, Vienna, Austria.
Michael GruschInstitute of Cancer Research, Department of Medicine I, Medical University of Vienna, Vienna, Austria.
Karin SchelchInstitute of Cancer Research, Department of Medicine I, Medical University of Vienna, Vienna, Austria.
Balazs HegedusDepartment of Thoracic Surgery, Ruhrlandklinik, University Clinic Essen, Essen, Germany.
Ildiko HorvathNational Koranyi Institute of Pulmonology, Budapest, Hungary.
Nandor BaranyNational Koranyi Institute of Pulmonology, Budapest, Hungary.
Zsolt MegyesfalviNational Koranyi Institute of Pulmonology, Budapest, Hungary.
Anna TiszaNational Koranyi Institute of Pulmonology, Budapest, Hungary.
Zoltan LohinaiNational Koranyi Institute of Pulmonology, Budapest, Hungary.
Mir Alireza HodaDepartment of Thoracic Surgery, Medical University of Vienna, Vienna, Austria.
Konrad HoetzeneckerDepartment of Thoracic Surgery, Medical University of Vienna, Vienna, Austria.
Francesco PezzellaNuffield Division of Laboratory Science, Radcliffe Department of Medicine, University of Oxford, John Radcliffe Hospital, Oxford, UK.
Sandor Paku1st Department of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary.
Viktoria LaszloNational Koranyi Institute of Pulmonology, Budapest, Hungary.
Balazs DomeNational Koranyi Institute of Pulmonology, Budapest, Hungary.
Medical University of Vienna · ATOrszágos Korányi Tbc és Pulmonológiai Intézet · HUEötvös Loránd University · HUSemmelweis University · HUNational Institute of Oncology · HURuhrlandklinik · DEUniversity of Kansas Medical Center · US

Funding

Austrian Science Fund FWF I 3977
6 · The paper itself

Abstract

Background: The microanatomical steps of malignant pleural mesothelioma (MPM) vascularization and the resistance mechanisms to anti-angiogenic drugs in MPM are unclear. Methods: We investigated the vascularization of intrapleurally implanted human P31 and SPC111 MPM cells. We also assessed MPM cell's motility, invasion and interaction with endothelial cells Results: P31 cells exhibited significantly higher two-dimensional (2D) motility and three-dimensional (3D) invasion than SPC111 cells Conclusions: Here, we report two distinct growth patterns of orthotopically implanted human MPM xenografts. In the invasive pattern, MPM cells invade and thus co-opt peritumoral capillary plexuses. In the pushing/desmoplastic pattern, MPM cells induce a desmoplastic response within the underlying tissue which allows the ingrowth of a nutritive vasculature from the pleura.

Indexed as

angiogenesisMesotheliomaorthotopic mouse model of mesotheliomavascularization

Identifiers

PMID35832452
PMCPMC9271443
OpenAlexW4285502997

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.