Evidence map›Paper›PMID 32671954›Full record

ArticleCancer reports (Hoboken, N.J.)2020

The Mini-Organo: A rapid high-throughput 3D coculture organotypic assay for oncology screening and drug development.

Jessica L Chitty, Joanna N Skhinas, Elysse C Filipe, Shan Wang, Carmen Rodriguez Cupello, Rhiannon D Grant, Michelle Yam, Michael Papanicolaou, Gretel Major, Anaiis Zaratzian and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Cancer reports (Hoboken, N.J.), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.7field-weighted citation impact, top 27% 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

11 citing papers in PubMed, 13 citations in OpenAlex.

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  9. Advanced Multi-Dimensional Cellular Models as Emerging Reality to ReproduceInternational journal of molecular sciences · 2021
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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

16 authors at 3 institutions in 3 countries.

Jessica L ChittyThe Garvan Institute of Medical Research and the Kinghorn Cancer Centre, Sydney, NSW, Australia.ORCID 0000-0003-1776-1618
Joanna N SkhinasThe Garvan Institute of Medical Research and the Kinghorn Cancer Centre, Sydney, NSW, Australia.ORCID 0000-0001-8797-8228
Elysse C FilipeThe Garvan Institute of Medical Research and the Kinghorn Cancer Centre, Sydney, NSW, Australia.ORCID 0000-0003-1956-0852
Shan WangDepartment of Laboratory Medicine, Division of Translational Cancer Research, Lund University, Lund, Sweden.
Carmen Rodriguez CupelloDepartment of Laboratory Medicine, Division of Translational Cancer Research, Lund University, Lund, Sweden.ORCID 0000-0003-3611-2496
Rhiannon D GrantThe Garvan Institute of Medical Research and the Kinghorn Cancer Centre, Sydney, NSW, Australia.
Michelle YamThe Garvan Institute of Medical Research and the Kinghorn Cancer Centre, Sydney, NSW, Australia.
Michael PapanicolaouThe Garvan Institute of Medical Research and the Kinghorn Cancer Centre, Sydney, NSW, Australia.
Gretel MajorThe Garvan Institute of Medical Research and the Kinghorn Cancer Centre, Sydney, NSW, Australia.
Anaiis ZaratzianThe Garvan Institute of Medical Research and the Kinghorn Cancer Centre, Sydney, NSW, Australia.
Andrew M Da SilvaThe Garvan Institute of Medical Research and the Kinghorn Cancer Centre, Sydney, NSW, Australia.
Michael TayaoThe Garvan Institute of Medical Research and the Kinghorn Cancer Centre, Sydney, NSW, Australia.
Claire VenninThe Garvan Institute of Medical Research and the Kinghorn Cancer Centre, Sydney, NSW, Australia.ORCID 0000-0001-9088-4177
Paul TimpsonThe Garvan Institute of Medical Research and the Kinghorn Cancer Centre, Sydney, NSW, Australia.ORCID 0000-0002-5514-7080
Chris D MadsenDepartment of Laboratory Medicine, Division of Translational Cancer Research, Lund University, Lund, Sweden.ORCID 0000-0001-6838-2103
Thomas R CoxThe Garvan Institute of Medical Research and the Kinghorn Cancer Centre, Sydney, NSW, Australia.ORCID 0000-0001-9294-1745
Garvan Institute of Medical Research · AULund University · SEUniversity of Technology Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe use of in vitro cell cultures is a powerful tool for obtaining key insights into the behaviour and response of cells to interventions in normal and disease situations. Unlike in vivo settings, in vitro experiments allow a fine-tuned control of a range of microenvironmental elements independently within an isolated setting. The recent expansion in the use of three-dimensional (3D) in vitro assays has created a number of representative tools to study cell behaviour in a more physiologically 3D relevant microenvironment. Complex 3D in vitro models that can recapitulate human tissue biology are essential for understanding the pathophysiology of disease.

aimThe development of the 3D coculture collagen contraction and invasion assay, the "organotypic assay," has been widely adopted as a powerful approach to bridge the gap between standard two-dimensional tissue culture and in vivo mouse models. In the cancer setting, these assays can then be used to dissect how stromal cells, such as cancer-associated fibroblasts (CAFs), drive extracellular matrix (ECM) remodelling to alter cancer cell behaviour and response to intervention. However, to date, many of the published organotypic protocols are low-throughput, time-consuming (up to several weeks), and work-intensive with often limited scalability. Our aim was to develop a fast, high-throughput, scalable 3D organotypic assay for use in oncology screening and drug development. METHODS AND

resultsHere, we describe a modified 96-well organotypic assay, the "Mini-Organo," which can be easily completed within 5 days. We demonstrate its application in a wide range of mouse and human cancer biology approaches including evaluation of stromal cell 3D ECM remodelling, 3D cancer cell invasion, and the assessment of efficacy of potential anticancer therapeutic targets. Furthermore, the organotypic assay described is highly amenable to customisation using different cell types under diverse experimental conditions.

conclusionsThe Mini-Organo high-throughput 3D organotypic assay allows the rapid screening of potential cancer therapeutics in human and mouse models in a time-efficient manner.

Indexed as

AnimalsCancer-Associated FibroblastsCoculture TechniquesDrug DevelopmentDrug Screening Assays, AntitumorHigh-Throughput Screening AssaysHumansMiceNeoplasm InvasivenessRats3D modelcancer-associated fibroblastcoculturedrug screeningextracellular matrixorganotypic

Identifiers

PMID32671954
PMCPMC7941459
OpenAlexW2964472826

What OpenQuestion holds

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LicenceCC BY-NC
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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.