Heterogeneity of Cholangiocarcinoma Immune Biology.

cancer stem cells cancer-associated fibroblasts cholangiocarcinoma heterogeneity immune cells liver tumor microenvironment

Journal

Cells
ISSN: 2073-4409
Titre abrégé: Cells
Pays: Switzerland
ID NLM: 101600052

Informations de publication

Date de publication:
08 03 2023
Historique:
received: 02 02 2023
revised: 04 03 2023
accepted: 06 03 2023
medline: 30 3 2023
entrez: 29 3 2023
pubmed: 30 3 2023
Statut: epublish

Résumé

Cholangiocarcinomas (CCAs) are aggressive tumors arising along the biliary tract epithelium, whose incidence and mortality are increasing. CCAs are highly desmoplastic cancers characterized by a dense tumor microenvironment (TME), in which each single component plays a fundamental role in shaping CCA initiation, progression and resistance to therapies. The crosstalk between cancer cells and TME can affect the recruitment, infiltration and differentiation of immune cells. According to the stage of the disease and to intra- and inter-patient heterogeneity, TME may contribute to either protumoral or antitumoral activities. Therefore, a better understanding of the effect of each immune cell subtype may open the path to new personalized immune therapeutic strategies for the management of CCA. In this review, we describe the role of immune cells in CCA initiation and progression, and their crosstalk with both cancer-associated fibroblasts (CAFs) and the cancer-stem-cell-like (CSC) niche.

Identifiants

pubmed: 36980187
pii: cells12060846
doi: 10.3390/cells12060846
pmc: PMC10047186
pii:
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Déclaration de conflit d'intérêts

CB receives honoraria from Astrazeneca (consultant, speaker, spouse employee), Incyte (consultant, speaker), Servier (consultant), Boehringer–Ingelheim (consultant); she receives research funds from Avacta, Medannex and Servier. JMB declares research grants (from Incyte and Albireo), personal fees for lecturer (from Astrazeneca), and consulting role (for QED Therapeutics, Albireo, OWL Metabolomics, Ikan Biotech CIMABay) The other authors declare no conflicts of interest.

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Auteurs

Francesca Vita (F)

School of Cancer Sciences, University of Glasgow, Glasgow G61 1QH, UK.
Department of Oncology, University of Turin, 10043 Turin, Italy.

Irene Olaizola (I)

Department of Liver and Gastrointestinal Diseases, Biodonostia Health Research Institute-Donostia University Hospital, University of the Basque Country (UPV/EHU), 20014 San Sebastian, Spain.

Francesco Amato (F)

School of Cancer Sciences, University of Glasgow, Glasgow G61 1QH, UK.

Colin Rae (C)

School of Cancer Sciences, University of Glasgow, Glasgow G61 1QH, UK.

Sergi Marco (S)

School of Cancer Sciences, University of Glasgow, Glasgow G61 1QH, UK.

Jesus M Banales (JM)

Department of Liver and Gastrointestinal Diseases, Biodonostia Health Research Institute-Donostia University Hospital, University of the Basque Country (UPV/EHU), 20014 San Sebastian, Spain.
IKERBASQUE, Basque Foundation for Science, 48009 Bilbao, Spain.
National Institute for the Study of Liver and Gastrointestinal Diseases (CIBERehd, "Instituto de Salud Carlos III"), 28029 Madrid, Spain.
Department of Biochemistry and Genetics, School of Sciences, University of Navarra, 31008 Pamplona, Spain.

Chiara Braconi (C)

School of Cancer Sciences, University of Glasgow, Glasgow G61 1QH, UK.
Beatson West of Scotland Cancer Centre, Glasgow G12 0YN, UK.

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