The immune cell infiltrate in the tumour microenvironment of phaeochromocytomas and paragangliomas.


Journal

Endocrine-related cancer
ISSN: 1479-6821
Titre abrégé: Endocr Relat Cancer
Pays: England
ID NLM: 9436481

Informations de publication

Date de publication:
01 11 2022
Historique:
received: 25 07 2022
accepted: 16 08 2022
pubmed: 18 8 2022
medline: 24 9 2022
entrez: 17 8 2022
Statut: epublish

Résumé

Emerging evidence suggests the composition of the tumour microenvironment (TME) correlates with clinical outcome and that each tumour type has a unique TME including a variable population of inflammatory cells. We performed immunohistochemistry on 65 phaeochromocytoma and paraganglioma (PPGL) tumour samples with 20 normal adrenal medulla samples for comparison. The immune cells assessed were macrophages, lymphocytes and neutrophils, and we compared the proportion of infiltration of these immune cells with clinical and histopathological factors. There was a higher proportion of immune cells in tumour tissue compared to non-neoplastic adrenal medulla tissue, with a predominance of macrophages. There was a higher proportion of M2:M1 macrophages and T-helper lymphocytes in aggressive tumours compared to indolent ones. For SDHB-associated tumours, there was a higher proportion of M2 macrophage infiltration, with higher M2:M1 in aggressive SDHB PPGLs compared to indolent tumours. These data demonstrate that immune cells do infiltrate the TME of PPGLs, confirming that PPGLs are immunologically active tumours. Differences in the TME of PPGLs were observed between aggressive and indolent tumours. These differences could potentially be exploited as an aid in predicting tumour behaviour.

Identifiants

pubmed: 35975974
doi: 10.1530/ERC-22-0020
pmc: PMC9513653
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

589-598

Subventions

Organisme : Cancer Research UK
ID : C16420/A18066
Pays : United Kingdom

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Auteurs

N Tufton (N)

Centre for Endocrinology, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, Charterhouse Square, London, UK.
Department of Endocrinology, St Bartholomew's Hospital, Barts Health NHS Trust. West Smithfield, London, UK.

R J Hearnden (RJ)

Centre for Endocrinology, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, Charterhouse Square, London, UK.

D M Berney (DM)

Department of Pathology, Royal London Hospital, Whitechapel, London, UK.

W M Drake (WM)

Centre for Endocrinology, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, Charterhouse Square, London, UK.
Department of Endocrinology, St Bartholomew's Hospital, Barts Health NHS Trust. West Smithfield, London, UK.

L Parvanta (L)

Department of Endocrine Surgery, St Bartholomew's Hospital, Barts Health NHS Trust, West Smithfield, London, UK.

J P Chapple (JP)

Centre for Endocrinology, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, Charterhouse Square, London, UK.

S A Akker (SA)

Centre for Endocrinology, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, Charterhouse Square, London, UK.
Department of Endocrinology, St Bartholomew's Hospital, Barts Health NHS Trust. West Smithfield, London, UK.

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Classifications MeSH