Evidence map›Paper›PMID 41265860›Full record

ArticleACS biomaterials science & engineering2025

Structural Control for Tunable Hyperthermia-Induced Cellular Responses Using 3D-Printed Platforms.

Daniel Boyer, Hadas Shilo, Eliana Steinberg, Ofra Benny

Abstract read
In one paragraph

Article in ACS biomaterials science & engineering, 2025. 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
–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

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

4 authors.

Daniel BoyerInstitute of Drug Research, Hebrew University of Jerusalem School of Pharmacy, Faculty of Medicine, Jerusalem 9112102, Israel.
Hadas ShiloInstitute of Drug Research, Hebrew University of Jerusalem School of Pharmacy, Faculty of Medicine, Jerusalem 9112102, Israel.
Eliana SteinbergInstitute of Drug Research, Hebrew University of Jerusalem School of Pharmacy, Faculty of Medicine, Jerusalem 9112102, Israel.
Ofra BennyInstitute of Drug Research, Hebrew University of Jerusalem School of Pharmacy, Faculty of Medicine, Jerusalem 9112102, Israel.ORCID 0000-0002-2468-5978

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Three-dimensional (3D) printing technologies have revolutionized bioengineering by enabling the fabrication of complex, customized structures with high morphological compatibility for specific functions. Most advances in the materials aspect of 3D printing have focused on developing inks that provide high stability and precise deposition for specific printing techniques. A new generation of printable materials not only ensures structural and mechanical integrity, but also incorporates additional functionalities directly into the material. The integration of rational structural design with functional materials offers powerful tools for biomedical applications. In this study, we developed a platform for investigating thermoresponsiveness in cell culture. By inducing controllable, localized heating, we examined the effects of hyperthermia on cancer cells, an emerging treatment modality gaining increasing attention as a promising anticancer strategy. We demonstrate that structurally controlled 3D-printed objects composed of polymer and iron oxide (IO) can generate defined thermal gradients upon exposure to infrared irradiation, thereby inducing differential cellular responses. Using precise spatial control with Digital Light Processing (DLP) printing, we created hyperthermia models. We demonstrated that the experimental conditions can detect changes in cell sensitivity, showing that pre-exposure of cancer cells to the cryoprotective compound trehalose alters their heat resistance. Moreover, repeated thermal cycles promoted the emergence of a cell subpopulation with enhanced heat resistance and increased aggressiveness, highlighting the platform's ability to drive adaptive cell selection based on thermal tolerance. Our findings indicate that thermal conditioning via 3D-printed platforms can serve as a robust tool for studying cellular responses to hyperthermia and may contribute to optimizing hyperthermia-based cancer therapies.

Indexed as

Hyperthermia, InducedPrinting, Three-DimensionalCell Line, TumorHumans3D printingdigital light processing (DLP)hyperthermiairon oxide nanoparticlesstructure−function

Identifiers

PMID41265860
PMCPMC12690519

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.