# An Open-Source Automated Pipeline for Quantitative Morphological Analysis of 3D-Bioprinted Cancer Cell Spheroids

**Authors:** Pius N. Amartey, Jocelyn S. Kim, Yetunde I. Kayode, Glenn E. Simmons

PMC · DOI: 10.3390/mps9010021 · Methods and Protocols · 2026-02-02

## TL;DR

This paper introduces an open-source pipeline for analyzing 3D-printed cancer cell spheroids to study tumor behavior and drug responses.

## Contribution

A detailed, automated protocol for 3D bioprinting and analyzing cancer spheroids using GelMA and open-source software.

## Key findings

- The method enables high-throughput and reproducible 3D spheroid culture formation.
- A customized CellProfiler pipeline allows quantitative morphological analysis of printed spheroids.
- The platform supports studies on metastasis, drug resistance, and tumor microenvironment features.

## Abstract

Three-dimensional (3D) culture systems that recapitulate the tumor microenvironment are essential for studying cancer cell behavior, drug response, and cell–matrix interactions. Here, we present a detailed protocol for generating 3D spheroid cultures from murine breast cancer cells using methacrylated gelatin (GelMA)-based bioink and a CELLINK BioX bioprinter. This method enables precise deposition of spheroid-laden GelMA droplets into low-attachment plates, facilitating high-throughput and reproducible 3D culture formation. The protocol includes steps for spheroid formation, GelMA preparation, bioprinting, and post-printing analysis using a customized CellProfiler pipeline. The analysis pipeline takes advantage of the functionality of CellProfiler and ImageJ software (version 2.14.0) packages to create a versatile and accessible analysis tool. This approach provides a robust and adaptable platform for in vitro cancer research, including studies of metastasis, drug resistance, cancer cell lipid metabolism, and TME-associated hypoxia.

## Linked entities

- **Diseases:** breast cancer (MONDO:0004989)

## Full-text entities

- **Genes:** Vim (vimentin) [NCBI Gene 22352], Cdh2 (cadherin 2) [NCBI Gene 12558] {aka CDHN, N-CAD, Ncad}, Zeb1 (zinc finger E-box binding homeobox 1) [NCBI Gene 21417] {aka 3110032K11Rik, AREB6, BZP, MEB1, Nil2, TCF-8}, elap (eye lens aplasia) [NCBI Gene 13708] {aka lap}
- **Diseases:** OA (MESH:D011015), Breast Cancer (MESH:D001943), solid (MESH:D018250), metastasis (MESH:D009362), hypoxic (MESH:D002534), mammary tumor (MESH:D015674), hypoxia (MESH:D000860), injury to (MESH:D014947), Cancer (MESH:D009369)
- **Chemicals:** Lipid (MESH:D008055), CO2 (MESH:D002245), OA (MESH:D019301), penicillin (MESH:D010406), unsaturated fatty acid (MESH:D005231), Falcon (-), DS (MESH:D003903), monounsaturated fatty acids (MESH:D005229), fatty acids (MESH:D005227), amino acids (MESH:D000596), water (MESH:D014867), oxygen (MESH:D010100), streptomycin (MESH:D013307), EDTA (MESH:D004492)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** Cat — Felis catus (Cat), Finite cell line (CVCL_XB61)

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12922002/full.md

## References

26 references — full list in the complete paper: https://tomesphere.com/paper/PMC12922002/full.md

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Source: https://tomesphere.com/paper/PMC12922002