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Table · dataset · 2026

Supplementary file 1_Proof-of-concept validation and characterisation of a DLP 3D bioprinted vascularised colorectal cancer model.docx

Listed in ZivaHub and Deakin Research Online and DMU Figshare and HKU DataHub and Swinburne Figshare and DaYta Ya Rona and SUNScholarData and figshare and Loughborough Research Repository and GRANTS Data and UP Research Data Repository — shown once because both records carry DOI 10.3389/fbioe.2026.1944341.s001

<p>Tumor vascularisation is essential in promoting cancer growth and metastasis and represents a key target for efficient drug delivery.

Description

Nevertheless, in vitro experimental models are limited to monolayer (co)cultures of endothelial and malignant cells, scratch and transwell migration assays where the vascularisation process is largely neglected. Direct contacts between different cell types and extracellular matrix (ECM) components, and processes like cell migration and invasion and ECM remodeling are also difficult to reproduce using conventional culturing methods.

This study aims to address some of these limitations by developing digital light processing (DLP) 3D bioprinted model of colorectal cancer based on methacrylated gelatin (GelMA) and containing endothelialised channels. The materials and approaches proposed here were additionally validated with 3D biofabricated in-house made designs based on the (bio)casting of GelMA and collagen hydrogels, and with 3D printed transwell assays.

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We found that our DLP bioprinting and 3D biofabrication protocols support the growth of HCT-116 colorectal cancer cells (embedded in the gel) and the survival of HUVEC endothelial cells (seeded to the channels), that cells adhere well to the collagen and GelMA matrices, and that the cells can remodel the hydrogel as revealed by scanning electron microscopy (SEM). Importantly, we also found that HUVECs migrate through these substrates in both the channel and transwell constructs.

Altogether, to our knowledge, this pilot study presents the first DLP bioprinted model of CRC using GelMA, and the only DLP bioprinted colorectal cancer model seeded with HUVECs suitable for in vitro study of tumor vascularisation and drug delivery.</p>

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Inferred from text
Cancer 75% · Microscopy 75% · Oncology and carcinogenesis 71%
Provenance · 11 source records, 57 field assertions
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