Human Immunocompetent Model of Neuroendocrine Liver Metastases Recapitulates Patient-Specific Tumour Microenvironment.

ex vivo model immune checkpoint receptor neuroendocrine liver metastases soluble immunomodulators tissue slices tumour modeling

Journal

Frontiers in endocrinology
ISSN: 1664-2392
Titre abrégé: Front Endocrinol (Lausanne)
Pays: Switzerland
ID NLM: 101555782

Informations de publication

Date de publication:
2022
Historique:
received: 31 03 2022
accepted: 07 06 2022
entrez: 1 8 2022
pubmed: 2 8 2022
medline: 3 8 2022
Statut: epublish

Résumé

Neuroendocrine liver metastases (LM-NEN) develop in a considerable proportion of patients with gastroenteropancreatic neuroendocrine neoplasms. There is a paucity of experimental models that accurately recapitulate this complex metastatic human liver microenvironment precluding scientific and clinical advancements. Here, we describe the development of a novel personalised immunocompetent precision cut tumour slice (PCTS) model for LM-NEN using resected human liver tissue. The histological assessment throughout the culture demonstrated that slices maintain viability for at least 7 days and retain the cellular heterogeneity of the original tumour. Essential clinical features, such as patient-specific histoarchitecture, tumour grade, neuroendocrine differentiation and metabolic capacity, are preserved in the slices. The PCTS also replicate the tumor-specific immunological profile as shown by the innate and adaptive immunity markers analysis. Furthermore, the study of soluble immune checkpoint receptors in the culture supernatants proves that these immunomodulators are actively produced by LM-NEN and suggests that this process is epithelium-dependent. This model can be employed to investigate these pathways and provides a powerful platform for mechanistic, immunological and pre-clinical studies.

Identifiants

pubmed: 35909511
doi: 10.3389/fendo.2022.909180
pmc: PMC9326114
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

909180

Informations de copyright

Copyright © 2022 Doornebal, Harris, Riva, Jagatia, Pizanias, Prachalias, Menon, Preziosi, Zamalloa, Miquel, Zen, Orford, Eaton, Heaton, Ramage, Palma, Srirajaskanthan and Chokshi.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Ewald Jan Doornebal (EJ)

Foundation for Liver Research, The Roger Williams Institute of Hepatology, London, United Kingdom.
King's College London, Faculty of Life Sciences and Medicine, London, United Kingdom.

Nicola Harris (N)

Foundation for Liver Research, The Roger Williams Institute of Hepatology, London, United Kingdom.
King's College London, Faculty of Life Sciences and Medicine, London, United Kingdom.

Antonio Riva (A)

Foundation for Liver Research, The Roger Williams Institute of Hepatology, London, United Kingdom.
King's College London, Faculty of Life Sciences and Medicine, London, United Kingdom.

Ravi Jagatia (R)

Foundation for Liver Research, The Roger Williams Institute of Hepatology, London, United Kingdom.
King's College London, Faculty of Life Sciences and Medicine, London, United Kingdom.

Michail Pizanias (M)

Institute of Liver Studies, King's College Hospital and King's College London, London, United Kingdom.

Andreas Prachalias (A)

Institute of Liver Studies, King's College Hospital and King's College London, London, United Kingdom.

Krishna Menon (K)

Institute of Liver Studies, King's College Hospital and King's College London, London, United Kingdom.

Melissa Preziosi (M)

Institute of Liver Studies, King's College Hospital and King's College London, London, United Kingdom.

Ane Zamalloa (A)

Institute of Liver Studies, King's College Hospital and King's College London, London, United Kingdom.

Rosa Miquel (R)

Liver Histopathology Laboratory, Institute of Liver Studies, King's College Hospital, London, United Kingdom.

Yoh Zen (Y)

Liver Histopathology Laboratory, Institute of Liver Studies, King's College Hospital, London, United Kingdom.

Michael Robert Orford (MR)

Great Ormond Street Institute of Child Health, University College London, London, United Kingdom.

Simon Eaton (S)

Great Ormond Street Institute of Child Health, University College London, London, United Kingdom.

Nigel Heaton (N)

Institute of Liver Studies, King's College Hospital and King's College London, London, United Kingdom.

John Ramage (J)

Institute of Liver Studies, King's College Hospital and King's College London, London, United Kingdom.
Neuroendocrine Tumour Unit, ENETS Centre of Excellence, King's College Hospital, London, United Kingdom.

Elena Palma (E)

Foundation for Liver Research, The Roger Williams Institute of Hepatology, London, United Kingdom.
King's College London, Faculty of Life Sciences and Medicine, London, United Kingdom.

Rajaventhan Srirajaskanthan (R)

Institute of Liver Studies, King's College Hospital and King's College London, London, United Kingdom.
Neuroendocrine Tumour Unit, ENETS Centre of Excellence, King's College Hospital, London, United Kingdom.

Shilpa Chokshi (S)

Foundation for Liver Research, The Roger Williams Institute of Hepatology, London, United Kingdom.
King's College London, Faculty of Life Sciences and Medicine, London, United Kingdom.

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