Evidence map›Paper›PMID 42471746›Full record

ArticleMacromolecular bioscience2026

Mimicking the Osteosarcoma Bone Microenvironment Using MEW-Printed PCL Scaffolds.

Chen Ye, Sabine Schulze, Richard Frank Richter, Max von Witzleben, Anne Weidlich, Hagen Fritzsche, Klaus-Dieter Schaser

Abstract read
In one paragraph

Article in Macromolecular bioscience, 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
–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

7 authors.

Chen YeUniversity Center of Orthopaedic, Trauma and Plastic Surgery, University Hospital Carl Gustav Carus and Faculty of Medicine at TUD Dresden University of Technology, Dresden, Germany.ORCID https://orcid.org/0009-0003-0704-4540
Sabine SchulzeUniversity Center of Orthopaedic, Trauma and Plastic Surgery, University Hospital Carl Gustav Carus and Faculty of Medicine at TUD Dresden University of Technology, Dresden, Germany.
Richard Frank RichterCenter for Translational Bone, Joint and Soft Tissue Research, University Hospital Carl Gustav Carus and Faculty of Medicine at TUD Dresden University of Technology, Dresden, Germany.ORCID https://orcid.org/0000-0002-3734-665X
Max von WitzlebenCenter for Translational Bone, Joint and Soft Tissue Research, University Hospital Carl Gustav Carus and Faculty of Medicine at TUD Dresden University of Technology, Dresden, Germany.ORCID https://orcid.org/0000-0001-9803-4679
Anne WeidlichUniversity Center of Orthopaedic, Trauma and Plastic Surgery, University Hospital Carl Gustav Carus and Faculty of Medicine at TUD Dresden University of Technology, Dresden, Germany.
Hagen FritzscheUniversity Center of Orthopaedic, Trauma and Plastic Surgery, University Hospital Carl Gustav Carus and Faculty of Medicine at TUD Dresden University of Technology, Dresden, Germany.
Klaus-Dieter SchaserUniversity Center of Orthopaedic, Trauma and Plastic Surgery, University Hospital Carl Gustav Carus and Faculty of Medicine at TUD Dresden University of Technology, Dresden, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteosarcoma is the most common primary malignant bone tumor, typically affecting children and adolescents during rapid growth periods. With current treatments, the five-year survival rate for metastatic or recurrent cases remains only 20-30%, highlighting the need for new therapeutic approaches and better preclinical models. Our goal is to simulate the osteosarcoma bone microenvironment using melt electrowriting (MEW)-printed polycaprolactone (PCL) scaffolds with optimized calcium phosphate formation. To achieve this, we fabricated PCL scaffolds with distinct MEW micro-architectures, including rectangular, triangular, and hexagonal designs with comparable primary fiber spacing, and investigated two calcium phosphate formation methods: natural cell-generated mineralization and direct calcium phosphate cement coating. Using SaOS-2 osteosarcoma cells, we systematically evaluated cell behavior, mineralization dynamics, and scaffold mechanical properties. This approach aims to establish a biomimetic 3D model that bridges the gap between laboratory findings and clinical applications, enabling more pathophysiologically relevant drug testing platforms.

Indexed as

Bone NeoplasmsOsteosarcomaPolyestersPrinting, Three-DimensionalTissue ScaffoldsTumor MicroenvironmentCalcium PhosphatesCell Line, TumorHumanscalcium phosphateCalcium PhosphatespolycaprolactonePolyestersbone microenvironmentMEW (melt electrowriting)osteosarcomaPCL (polycaprolactone)SaOS‐2 cells

Identifiers

PMID42471746
PMCPMC13380633

What Socratic 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 Socratic graph.