Evidence map›Paper›PMID 35625969›Full record

ArticleCancers2022

Multiphoton Microscopy Reveals DAPK1-Dependent Extracellular Matrix Remodeling in a Chorioallantoic Membrane (CAM) Model.

Philipp Kunze, Lucas Kreiss, Vendula Novosadová, Adriana V Roehe, Sara Steinmann, Jan Prochazka, Carol I Geppert, Arndt Hartmann, Sebastian Schürmann, Oliver Friedrich and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. 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
1.0field-weighted citation impact, top 25% 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.

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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

11 authors at 3 institutions in 3 countries.

Philipp KunzeExperimental Tumor Pathology, Institute of Pathology, University Hospital Erlangen, Friedrich-Alexander University Erlangen-Nürnberg (FAU), 91054 Erlangen, Germany.
Lucas KreissInstitute of Medical Biotechnology, Friedrich-Alexander University Erlangen-Nürnberg (FAU), Paul-Gordan-Str. 3, 91052 Erlangen, Germany.ORCID 0000-0002-7749-0015
Vendula NovosadováCzech Center for Phenogenomics, Institute of Molecular Genetics of the ASCR, 142 20 Prague, Czech Republic.
Adriana V RoeheDepartment of Pathology and Legal Medicine, Federal University of Health Sciences of Porto Alegre, Porto Alegre 90050-170, Brazil.ORCID 0000-0002-6294-7342
Sara SteinmannExperimental Tumor Pathology, Institute of Pathology, University Hospital Erlangen, Friedrich-Alexander University Erlangen-Nürnberg (FAU), 91054 Erlangen, Germany.
Jan ProchazkaCzech Center for Phenogenomics, Institute of Molecular Genetics of the ASCR, 142 20 Prague, Czech Republic.
Carol I GeppertInstitute of Pathology, University Hospital Erlangen, Friedrich-Alexander University Erlangen-Nürnberg (FAU), 91054 Erlangen, Germany.
Arndt HartmannInstitute of Pathology, University Hospital Erlangen, Friedrich-Alexander University Erlangen-Nürnberg (FAU), 91054 Erlangen, Germany.
Sebastian SchürmannInstitute of Medical Biotechnology, Friedrich-Alexander University Erlangen-Nürnberg (FAU), Paul-Gordan-Str. 3, 91052 Erlangen, Germany.
Oliver FriedrichInstitute of Medical Biotechnology, Friedrich-Alexander University Erlangen-Nürnberg (FAU), Paul-Gordan-Str. 3, 91052 Erlangen, Germany.ORCID 0000-0003-2238-2049
Regine Schneider-StockExperimental Tumor Pathology, Institute of Pathology, University Hospital Erlangen, Friedrich-Alexander University Erlangen-Nürnberg (FAU), 91054 Erlangen, Germany.
Friedrich-Alexander-Universität Erlangen-Nürnberg · DECzech Academy of Sciences, Institute of Molecular Genetics · CZQueensland University of Technology · AU

Funding

Charles University CZ.1.05/1.1.00/02.0109Czech Academy of Sciences RVO 68378050European Cooperation in Science and Technology CA17118Ministry of Education, Youth and Sports of the Czech Republic LM2018126
6 · The paper itself

Abstract

Cancer cells facilitate tumor growth by creating favorable tumor micro-environments (TME), altering homeostasis and immune response in the extracellular matrix (ECM) of surrounding tissue. A potential factor that contributes to TME generation and ECM remodeling is the cytoskeleton-associated human death-associated protein kinase 1 (DAPK1). Increased tumor cell motility and de-adhesion (thus, promoting metastasis), as well as upregulated plasminogen-signaling, are shown when functionally analyzing the DAPK1 ko-related proteome. However, the systematic investigation of how tumor cells actively modulate the ECM at the tissue level is experimentally challenging since animal models do not allow direct experimental access while artificial in vitro scaffolds cannot simulate the entire complexity of tissue systems. Here, we used the chorioallantoic membrane (CAM) assay as a natural, collagen-rich tissue model in combination with all-optical experimental access by multiphoton microscopy (MPM) to study the ECM remodeling potential of colorectal tumor cells with and without DAPK1 in situ and even in vivo. This approach demonstrates the suitability of the CAM assay in combination with multiphoton microscopy for studying collagen remodeling during tumor growth. Our results indicate the high ECM remodeling potential of DAPK1 ko tumor cells at the tissue level and support our findings from proteomics.

Indexed as

collagencolon cancerECM remodelingMPMuPAR

Identifiers

PMID35625969
PMCPMC9139596
OpenAlexW4280570289

What OpenQuestion holds

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Registered trials

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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.