Evidence map›Paper›PMID 42764445›Full record

ArticleAdvanced healthcare materials2026

A Hybrid Bioprinting-Microfabrication Approach to Controllable Multitype Spheroid Arrays for Modeling Tumor Heterogeneity.

Simone Bonetti, Eva Clemente, Emanuela Mensà, Marco de Maria, Fulvia Farabegoli, Emanuela Saracino, Barbara Bortolani, Emanuela Marcelli, Renato Brandimarti, Dario de Biase and 1 more

Abstract read
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In one paragraph

Article in Advanced healthcare materials, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Simone BonettiInstitute for the Study of Nanostructured Materials, National Research Council of Italy, Bologna, Italy.ORCID https://orcid.org/0000-0002-6341-4185
Eva ClementeInstitute for the Study of Nanostructured Materials, National Research Council of Italy, Bologna, Italy.ORCID https://orcid.org/0000-0001-7344-2529
Emanuela MensàDepartment of Pharmacy and Biotechnology, University of Bologna, Bologna, Italy.ORCID https://orcid.org/0000-0002-3284-6161
Marco de MariaDepartment of Pharmacy and Biotechnology, University of Bologna, Bologna, Italy.ORCID https://orcid.org/0009-0008-2979-1383
Fulvia FarabegoliDepartment of Pharmacy and Biotechnology, University of Bologna, Bologna, Italy.ORCID https://orcid.org/0000-0001-6254-9443
Emanuela SaracinoInstitute for the Organic Synthesis and Photoreactivity, National Research Council of Italy, Bologna, Italy.ORCID https://orcid.org/0000-0001-9140-3128
Barbara BortolanieDIMES Lab - DIMEC, Policlinico S. Orsola-Malpighi, University of Bologna, Bologna, Italy.ORCID https://orcid.org/0000-0003-1240-9391
Emanuela MarcellieDIMES Lab - DIMEC, Policlinico S. Orsola-Malpighi, University of Bologna, Bologna, Italy.ORCID https://orcid.org/0000-0002-5897-003X
Renato BrandimartiDepartment of Pharmacy and Biotechnology, University of Bologna, Bologna, Italy.ORCID https://orcid.org/0000-0003-3078-9009
Dario de BiaseDepartment of Pharmacy and Biotechnology, University of Bologna, Bologna, Italy.ORCID https://orcid.org/0000-0002-0609-8817
Giampaolo ZuccheriDepartment of Pharmacy and Biotechnology, University of Bologna, Bologna, Italy.ORCID https://orcid.org/0000-0003-4777-5391

Funding

PRIN PNRR 2022 20224KF8HEProgetto Metodi Alternativi 2022 of the University of Bologna (funded by The Italian Ministry of Health)
6 · The paper itself

Abstract

The intrinsic heterogeneity of solid tumors remains a crucial barrier to understanding cancer biology and predicting therapeutic outcomes. Here, we introduce a scalable and versatile biofabrication platform that enables the controlled assembly of multitype spheroid arrays (MSA) within standard culture microplates. By performing programmable bioprinting within soft, microstructured culture devices, we achieve the precise spatial deposition of multiple cell types into defined microwells, yielding reproducible arrays of heterogeneous 3D tumor spheroids that collectively recapitulate the macro- and micro-heterogeneity of solid cancers. We demonstrate that this approach permits the fine-tuning of spheroid size, composition, and arrangement. It also supports the delayed secondary programmed seeding of cells on pre-grown spheroids, mimicking biological processes such as the invasion of immune cells. These methods enable quantitative drug-response profiling within a single assay. They overcome some critical limitations of current 3D cancer models, introducing the concept of the "cancer-in-a-well" technology. This technology provides a simple-to-use, cost-effective, high-throughput, and highly reproducible platform to recreate the complexity of tumors in vitro using methods and instruments that can be potentially used by any researcher in any cell culture lab. We can foresee a positive impact on cancer biology studies, drug screening, and personalized oncology.

Indexed as

BioprintingModels, BiologicalNeoplasmsSpheroids, CellularCell Line, TumorHumans3D culturebioprintingcancer modelingtumor heterogeneitytumor microenvironmenttumor spheroids

Identifiers

PMID42764445

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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.