Cholangiocarcinoma-on-a-chip: A human 3D platform for personalised medicine.

Cell–cell crosstalk Cholangiocarcinoma Drug testing Liver-on-chip Microfluidics Tumour microenvironment

Journal

JHEP reports : innovation in hepatology
ISSN: 2589-5559
Titre abrégé: JHEP Rep
Pays: Netherlands
ID NLM: 101761237

Informations de publication

Date de publication:
Jan 2024
Historique:
received: 12 06 2023
revised: 15 08 2023
accepted: 31 08 2023
medline: 11 12 2023
pubmed: 11 12 2023
entrez: 11 12 2023
Statut: epublish

Résumé

Cholangiocarcinoma (CCA) is a primary liver tumour characterised by a poor prognosis and limited therapeutic options. Available 3D human CCA models fail to faithfully recapitulate the tumour niche. We aimed to develop an innovative patient-specific CCA-on-chip platform. A CCA tumour microenvironment was recapitulated on a microfluidic three-channel chip using primary CCA cells, cancer-associated fibroblasts (CAFs), endothelial cells, and T cells isolated from CCA specimens (n = 6). CAF and CCA cells were co-cultured in the central channel, flanked by endothelial cells in one lateral channel, recreating a tubular structure. An extensive characterisation of this platform was carried out to investigate its diffusion ability, hydrogel properties, and changes in matrix composition. Cell phenotype and functional properties were assessed. Primary cells seeded on the microfluidic device were shown to reproduce the architectural structure and maintain the original phenotype and functional properties. The tumour niche underwent a deep remodelling in the 3D device, with an increase in hydrogel stiffness and extracellular matrix deposition, mimicking We presented a 3D CCA platform that integrates the major non-immune components of the tumour microenvironment and the T cell infiltrate, reflecting the CCA niche. This CCA-on-chip represents a reliable patient-specific 3D platform that will be of help to further elucidate the biological mechanisms involved in CCA and provide an efficient tool for personalised drug testing. An innovative patient-specific cholangiocarcinoma (CCA)-on-chip platform was successfully developed, integrating the major components of the tumour microenvironment (tumour cells, cancer-associated fibroblasts, endothelial cells, and immune infiltrate) and faithfully mimicking the CCA niche. This CCA-on-chip represents a powerful tool for unravelling disease-associated cellular mechanisms in CCA and provides an efficient tool for personalised drug testing.

Sections du résumé

Background & Aims UNASSIGNED
Cholangiocarcinoma (CCA) is a primary liver tumour characterised by a poor prognosis and limited therapeutic options. Available 3D human CCA models fail to faithfully recapitulate the tumour niche. We aimed to develop an innovative patient-specific CCA-on-chip platform.
Methods UNASSIGNED
A CCA tumour microenvironment was recapitulated on a microfluidic three-channel chip using primary CCA cells, cancer-associated fibroblasts (CAFs), endothelial cells, and T cells isolated from CCA specimens (n = 6). CAF and CCA cells were co-cultured in the central channel, flanked by endothelial cells in one lateral channel, recreating a tubular structure. An extensive characterisation of this platform was carried out to investigate its diffusion ability, hydrogel properties, and changes in matrix composition. Cell phenotype and functional properties were assessed.
Results UNASSIGNED
Primary cells seeded on the microfluidic device were shown to reproduce the architectural structure and maintain the original phenotype and functional properties. The tumour niche underwent a deep remodelling in the 3D device, with an increase in hydrogel stiffness and extracellular matrix deposition, mimicking
Conclusions UNASSIGNED
We presented a 3D CCA platform that integrates the major non-immune components of the tumour microenvironment and the T cell infiltrate, reflecting the CCA niche. This CCA-on-chip represents a reliable patient-specific 3D platform that will be of help to further elucidate the biological mechanisms involved in CCA and provide an efficient tool for personalised drug testing.
Impact and implications UNASSIGNED
An innovative patient-specific cholangiocarcinoma (CCA)-on-chip platform was successfully developed, integrating the major components of the tumour microenvironment (tumour cells, cancer-associated fibroblasts, endothelial cells, and immune infiltrate) and faithfully mimicking the CCA niche. This CCA-on-chip represents a powerful tool for unravelling disease-associated cellular mechanisms in CCA and provides an efficient tool for personalised drug testing.

Identifiants

pubmed: 38074504
doi: 10.1016/j.jhepr.2023.100910
pii: S2589-5559(23)00241-0
pmc: PMC10698278
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100910

Informations de copyright

© 2023 The Author(s).

Déclaration de conflit d'intérêts

AL reports receiving consulting fees from Advanz Pharma, AlfaSigma, Takeda, and Albireo Pharma, and speaker fees from Gilead, AbbVie, MSD, Intercept Pharma, AlfaSigma, GSK, and Incyte. All other authors declare no conflicts of interest. Please refer to the accompanying ICMJE disclosure forms for further details.

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Auteurs

Michela Anna Polidoro (MA)

Hepatobiliary Immunopathology Laboratory, IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.

Erika Ferrari (E)

Department of Electronics, Information and Bioengineering, Politecnico di Milano, Milan, Italy.

Cristiana Soldani (C)

Hepatobiliary Immunopathology Laboratory, IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.

Barbara Franceschini (B)

Hepatobiliary Immunopathology Laboratory, IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.

Giuseppe Saladino (G)

Department of Electronics, Information and Bioengineering, Politecnico di Milano, Milan, Italy.

Arianna Rosina (A)

Department of Electronics, Information and Bioengineering, Politecnico di Milano, Milan, Italy.

Andrea Mainardi (A)

Department of Electronics, Information and Bioengineering, Politecnico di Milano, Milan, Italy.
Department of Biomedicine, University Hospital Basel, University of Basel, Basel, Switzerland.

Francesca D'Autilia (F)

Unit of Advanced Optical Microscopy, IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.

Nicola Pugliese (N)

Department of Biomedical Science, Humanitas University, Pieve Emanuele, Milan, Italy.
Division of Internal Medicine and Hepatology, Department of Gastroenterology, IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.

Guido Costa (G)

Division of Hepatobiliary and General Surgery, Department of Surgery, IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.

Matteo Donadon (M)

Department of Health Sciences, Università del Piemonte Orientale, Novara, Italy.
Department of General Surgery, University Maggiore Hospital, Novara, Italy.

Guido Torzilli (G)

Department of Biomedical Science, Humanitas University, Pieve Emanuele, Milan, Italy.
Division of Hepatobiliary and General Surgery, Department of Surgery, IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.

Simona Marzorati (S)

Hepatobiliary Immunopathology Laboratory, IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.

Marco Rasponi (M)

Department of Electronics, Information and Bioengineering, Politecnico di Milano, Milan, Italy.

Ana Lleo (A)

Department of Biomedical Science, Humanitas University, Pieve Emanuele, Milan, Italy.
Division of Internal Medicine and Hepatology, Department of Gastroenterology, IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.

Classifications MeSH