Evidence map›Paper›PMID 41993623›Full record

ArticleTheranostics2026

Tailorable porous collagen hydrogels as a physiologically relevant platform for extrachromosomal DNA-associated colorectal cancer research.

Seoyul Jo, Jiwon Shon, Seohyeon An, Yoonjoo Nam, Dongwon Choi, Seungmi Lee, Hoigi Seo, Se Young Chun, Hoon Kim, GeunHyung Kim

Abstract read
In one paragraph

Article in Theranostics, 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

10 authors.

Seoyul JoDepartment of Precision Medicine, Sungkyunkwan University School of Medicine (SKKU-SOM), Suwon 16419, South Korea.
Jiwon ShonDepartment of Biohealth Regulatory Science, School of Pharmacy, Sungkyunkwan University, Suwon, South Korea.
Seohyeon AnDepartment of Precision Medicine, Sungkyunkwan University School of Medicine (SKKU-SOM), Suwon 16419, South Korea.
Yoonjoo NamDepartment of Biopharmaceutical Convergence, School of Pharmacy, Sungkyunkwan University, Suwon, South Korea.
Dongwon ChoiDepartment of Pharmacy, School of Pharmacy, Sungkyunkwan University, Suwon-si, South Korea.
Seungmi LeeDepartment of Pharmacy, School of Pharmacy, Sungkyunkwan University, Suwon-si, South Korea.
Hoigi SeoDepartment of Electrical and Computer Engineering, Seoul National University, Seoul, South Korea.
Se Young ChunDepartment of Electrical and Computer Engineering, Seoul National University, Seoul, South Korea.
Hoon KimDepartment of Biohealth Regulatory Science, School of Pharmacy, Sungkyunkwan University, Suwon, South Korea.
GeunHyung KimDepartment of Precision Medicine, Sungkyunkwan University School of Medicine (SKKU-SOM), Suwon 16419, South Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A novel 3D porous hydrogel model, mimicking the tumor microenvironment (TME), was developed as a physiologically relevant platform to investigate the role of extrachromosomal DNA (ecDNA) in colorectal cancer. We fabricated a tailorable collagen-based hydrogel that overcomes the limitation of 2D cultures by enabling crucial cell-cell and cell-matrix interactions. Methods: First, we validated whether the selected COLO320 cell lines were suitable for investigation of ecDNA in 3D tumor model and confirmed that ecDNA structures were stably maintained under 3D culture conditions by whole genome sequencing (WGS). Additionally, to provide an appropriate environment for colorectal cancer cells, we fabricated collagen-based porous hydrogels using a whipping process that requires no surfactants or sacrificial materials. During this process, we optimized the bioink formulation to achieve extracellular matrix (ECM) stiffness favorable for colorectal cancer cell proliferation, aggregation, stem-like behavior, and epithelial-mesenchymal transition (EMT)-related gene expression. Results: By optimizing the porous structure for enhanced nutrient diffusion and cell infiltration, we successfully maintained ecDNA structures in COLO320 cells. Our optimized porous platform significantly enhanced cellular proliferation, aggregation, and metabolic activity compared to conventional bulk model. We also observed elevated expressions of key oncogenes like MYC and activation of mechanotransduction pathways associated with aggressive tumor phenotypes. Conclusion: This reproducible and effective model accurately reflects ecDNA-driven biological behaviors, making it ideal for long-term ecDNA research and future TME-related studies.

Indexed as

CollagenColorectal NeoplasmsHydrogelsCell Culture Techniques, Three DimensionalCell Line, TumorCell ProliferationEpithelial-Mesenchymal TransitionExtracellular MatrixExtrachromosomal DNAHumansPorosityTumor MicroenvironmentCollagenExtrachromosomal DNAHydrogels3D in vitro modelcollagen hydrogelextrachromosomal DNA (ecDNA)porous structuretumor microenvironment (TME)

Identifiers

PMID41993623
PMCPMC13080448

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.