Galectin-9 expression on tumour-associated immune cells is associated with favourable clinicopathological features and better outcomes in oral squamous cell carcinoma.

galectin-9 immunohistochemistry oral squamous cell carcinoma prognosis tumour micro-environment

Journal

Contemporary oncology (Poznan, Poland)
ISSN: 1428-2526
Titre abrégé: Contemp Oncol (Pozn)
Pays: Poland
ID NLM: 101233223

Informations de publication

Date de publication:
2023
Historique:
received: 18 04 2023
accepted: 19 04 2023
medline: 2 6 2023
pubmed: 2 6 2023
entrez: 2 6 2023
Statut: ppublish

Résumé

Galectin-9, a β-galactoside-binding protein, might be a potential target in cancer personalized therapy, but contradicting data exist regarding its prognostic significance in malignancy. Previous studies showed low or absent expression of galectin-9 on tumour cells of oral squamous cell carcinoma (OSCC); thus, we aimed to assess the prognostic impact of its expression on tumour-associated immune cells (TAICs). A retrospective analysis was conducted on 62 patients with OSCC. Tissue microarrays were constructed with chemo- and radiotherapy-naïve tissue samples and stained with anti-galectin-9 antibody. Cytoplasmic reactions in TAICs were counted as positive, and the percentage of galectin-9-positive cells was calculated. The expression of galectin-9 was not associated with any demographic factors, other than diabetes mellitus type 2, for which there were lower levels of expression (p = 0.029). Higher levels of galectin-9 were associated with less locally advanced tumours (p = 0.023) and lack of nodal metastases (p = 0.014). Galectin-9 expression positively correlated with PD-L1 expression on TAICs (p = 0.009). Patients with > 50% galectin-9-positive cells were determined to have a superior 5-year overall survival ( Future studies are necessary to investigate the effects of galectin-9 on the tumour micro-environment, and galectin-9-targeted treatment may be considered, especially with its correlation to PD-L1 in OSCC.

Identifiants

pubmed: 37266336
doi: 10.5114/wo.2023.127142
pii: 50629
pmc: PMC10230243
doi:

Types de publication

Journal Article

Langues

eng

Pagination

22-27

Informations de copyright

Copyright © 2023 Termedia.

Déclaration de conflit d'intérêts

The authors declare no conflict of interest.

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Auteurs

Rafał Pęksa (R)

Department of Pathomorphology, Medical University of Gdansk, Gdansk, Poland.

Michał Kunc (M)

Department of Pathomorphology, Medical University of Gdansk, Gdansk, Poland.

Michał Piątek (M)

Department of Oncology, Institute of Medical Sciences, University of Opole, Opole, Poland.

Barbara S Radecka (BS)

Department of Oncology, Institute of Medical Sciences, University of Opole, Opole, Poland.

Barbara Alicja Jereczek-Fossa (BA)

Division of Radiotherapy, IEO European Institute of Oncology, IRCCS, Milan, Italy.

Anna Starzyńska (A)

Department of Oral Surgery, Medical University of Gdansk, Gdansk, Poland.

Classifications MeSH