Evidence map›Paper›PMID 36929461›Full record

ArticleCellular and molecular life sciences : CMLS2023

Microstructured soft devices for the growth and analysis of populations of homogenous multicellular tumor spheroids.

Ottavia Tartagni, Alexandra Borók, Emanuela Mensà, Attila Bonyár, Barbara Monti, Johan Hofkens, Anna Maria Porcelli, Giampaolo Zuccheri

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In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

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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

8 authors.

Ottavia TartagniDepartment of Pharmacy and Biotechnology, University of Bologna, Via San Donato, 19/2, 40127, Bologna, Italy.ORCID http://orcid.org/0000-0003-4114-7511
Alexandra BorókDepartment of Electronics Technology, Budapest University of Technology and Economics, Budapest, Hungary.
Emanuela MensàDepartment of Pharmacy and Biotechnology, University of Bologna, Via San Donato, 19/2, 40127, Bologna, Italy.ORCID http://orcid.org/0000-0002-3284-6161
Attila BonyárDepartment of Electronics Technology, Budapest University of Technology and Economics, Budapest, Hungary.ORCID http://orcid.org/0000-0002-6976-7846
Barbara MontiDepartment of Pharmacy and Biotechnology, University of Bologna, Via San Donato, 19/2, 40127, Bologna, Italy.ORCID http://orcid.org/0000-0003-0330-482X
Johan HofkensDepartment of Chemistry, KU Leuven, 3001, Leuven, Belgium.ORCID http://orcid.org/0000-0002-9101-0567
Anna Maria PorcelliDepartment of Pharmacy and Biotechnology, University of Bologna, Via San Donato, 19/2, 40127, Bologna, Italy.ORCID http://orcid.org/0000-0002-6209-0692
Giampaolo ZuccheriDepartment of Pharmacy and Biotechnology, University of Bologna, Via San Donato, 19/2, 40127, Bologna, Italy. giampaolo.zuccheri@unibo.it.ORCID http://orcid.org/0000-0003-4777-5391

Funding

ALS Association 20-IIP-522Associazione Italiana per la Ricerca sul Cancro IG 2020-ID24494Regione Emilia-Romagna Ph.D. grants under POR FSE 2014/2020UNA Europa Interuniversity Alliance SF2019012
6 · The paper itself

Abstract

Multicellular tumor spheroids are rapidly emerging as an improved in vitro model with respect to more traditional 2D culturing. Microwell culturing is a simple and accessible method for generating a large number of uniformly sized spheroids, but commercially available systems often do not enable researchers to perform complete culturing and analysis pipelines and the mechanical properties of their culture environment are not commonly matching those of the target tissue. We herein report a simple method to obtain custom-designed self-built microwell arrays made of polydimethylsiloxane or agarose for uniform 3D cell structure generation. Such materials can provide an environment of tunable mechanical flexibility. We developed protocols to culture a variety of cancer and non-cancer cell lines in such devices and to perform molecular and imaging characterizations of the spheroid growth, viability, and response to pharmacological treatments. Hundreds of tumor spheroids grow (in scaffolded or scaffold-free conditions) at homogeneous rates and can be harvested at will. Microscopy imaging can be performed in situ during or at the end of the culture. Fluorescence (confocal) microscopy can be performed after in situ staining while retaining the geographic arrangement of spheroids in the plate wells. This platform can enable statistically robust investigations on cancer biology and screening of drug treatments.

Indexed as

NeoplasmsSpheroids, CellularCell LineCell Line, TumorHumans3D cell cultureCancer modelsDrug screeningHigh content screeningHigh-throughput screeningMicrotissuesMicrowellsSpheroid

Identifiers

PMID36929461
PMCPMC10020259

What Socratic holds

Textfull text, public
LicenceCC BY
measurements read85
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.