Evidence map›Paper›PMID 34734500›Full record

ArticleAdvanced healthcare materials2022

Modeling Metastatic Colonization in a Decellularized Organ Scaffold-Based Perfusion Bioreactor.

Maria Rafaeva, Edward R Horton, Adina R D Jensen, Chris D Madsen, Raphael Reuten, Oliver Willacy, Christian B Brøchner, Thomas H Jensen, Kamilla Westarp Zornhagen, Marina Crespo and 10 more

Open access · hybridAbstract read
In one paragraph

Article in Advanced healthcare materials, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

13 citing papers in PubMed, 17 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

20 authors at 3 institutions in 2 countries.

Maria RafaevaBiotech Research and Innovation Centre (BRIC), University of Copenhagen (UCPH), Ole Maaloes Vej 5, Copenhagen, 2200, Denmark.ORCID 0000-0002-7317-4058
Edward R HortonBiotech Research and Innovation Centre (BRIC), University of Copenhagen (UCPH), Ole Maaloes Vej 5, Copenhagen, 2200, Denmark.ORCID 0000-0001-9530-9585
Adina R D JensenBiotech Research and Innovation Centre (BRIC), University of Copenhagen (UCPH), Ole Maaloes Vej 5, Copenhagen, 2200, Denmark.ORCID 0000-0003-3739-6320
Chris D MadsenDivision of Translational Cancer Research, Department of Laboratory Medicine, Lund University, Lund, 22242, Sweden.ORCID 0000-0001-6838-2103
Raphael ReutenBiotech Research and Innovation Centre (BRIC), University of Copenhagen (UCPH), Ole Maaloes Vej 5, Copenhagen, 2200, Denmark.ORCID 0000-0002-9434-4108
Oliver WillacyBiotech Research and Innovation Centre (BRIC), University of Copenhagen (UCPH), Ole Maaloes Vej 5, Copenhagen, 2200, Denmark.
Christian B BrøchnerDepartment of Pathology, Rigshospitalet, Copenhagen University Hospital, Blegdamsvej 9, Copenhagen, 2100, Denmark.
Thomas H JensenDepartment of Pathology, Rigshospitalet, Copenhagen University Hospital, Blegdamsvej 9, Copenhagen, 2100, Denmark.
Kamilla Westarp ZornhagenBiotech Research and Innovation Centre (BRIC), University of Copenhagen (UCPH), Ole Maaloes Vej 5, Copenhagen, 2200, Denmark.
Marina CrespoBiotech Research and Innovation Centre (BRIC), University of Copenhagen (UCPH), Ole Maaloes Vej 5, Copenhagen, 2200, Denmark.
Dina S GrønsethBiotech Research and Innovation Centre (BRIC), University of Copenhagen (UCPH), Ole Maaloes Vej 5, Copenhagen, 2200, Denmark.
Sebastian R NielsenBiotech Research and Innovation Centre (BRIC), University of Copenhagen (UCPH), Ole Maaloes Vej 5, Copenhagen, 2200, Denmark.ORCID 0000-0002-8449-476X
Manja IdornNational Center for Cancer Immune Therapy (CCIT), Department of Oncology, University Hospital Herlev and Department of Immunology and Microbiology, University of Copenhagen (UCPH), Herlev Ringvej 75, Herlev, 2730, Denmark.
Per Thor StratenNational Center for Cancer Immune Therapy (CCIT), Department of Oncology, University Hospital Herlev and Department of Immunology and Microbiology, University of Copenhagen (UCPH), Herlev Ringvej 75, Herlev, 2730, Denmark.ORCID 0000-0002-4731-4969
Kristoffer RohrbergDepartment of Oncology, Centre for Cancer and Organ Diseases, Rigshospitalet, Copenhagen University Hospital, Blegdamsvej 9, Copenhagen, 2100, Denmark.
Iben SpanggaardDepartment of Oncology, Centre for Cancer and Organ Diseases, Rigshospitalet, Copenhagen University Hospital, Blegdamsvej 9, Copenhagen, 2100, Denmark.
Martin HøjgaardDepartment of Oncology, Centre for Cancer and Organ Diseases, Rigshospitalet, Copenhagen University Hospital, Blegdamsvej 9, Copenhagen, 2100, Denmark.
Ulrik LassenDepartment of Oncology, Centre for Cancer and Organ Diseases, Rigshospitalet, Copenhagen University Hospital, Blegdamsvej 9, Copenhagen, 2100, Denmark.
Janine T ErlerBiotech Research and Innovation Centre (BRIC), University of Copenhagen (UCPH), Ole Maaloes Vej 5, Copenhagen, 2200, Denmark.ORCID 0000-0001-8675-6527
Alejandro E Mayorca-GuilianiBiotech Research and Innovation Centre (BRIC), University of Copenhagen (UCPH), Ole Maaloes Vej 5, Copenhagen, 2200, Denmark.ORCID 0000-0001-8137-4722
University of Copenhagen · DKCopenhagen University Hospital · DKLund University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metastatic cancer spread is responsible for most cancer-related deaths. To colonize a new organ, invading cells adapt to, and remodel, the local extracellular matrix (ECM), a network of proteins and proteoglycans underpinning all tissues, and a critical regulator of homeostasis and disease. However, there is a major lack in tools to study cancer cell behavior within native 3D ECM. Here, an in-house designed bioreactor, where mouse organ ECM scaffolds are perfused and populated with cells that are challenged to colonize it, is presented. Using a specialized bioreactor chamber, it is possible to monitor cell behavior microscopically (e.g., proliferation, migration) within the organ scaffold. Cancer cells in this system recapitulate cell signaling observed in vivo and remodel complex native ECM. Moreover, the bioreactors are compatible with co-culturing cell types of different genetic origin comprising the normal and tumor microenvironment. This degree of experimental flexibility in an organ-specific and 3D context, opens new possibilities to study cell-cell and cell-ECM interplay and to model diseases in a controllable organ-specific system ex vivo.

Indexed as

Extracellular MatrixTissue ScaffoldsAnimalsBioreactorsMicePerfusionProteoglycansTissue EngineeringProteoglycanscancer metastasisexperimental methodsextracellular matrixspecialized bioreactors

Identifiers

PMID34734500
PMCPMC11469127
OpenAlexW3210600288

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.