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
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
22-27Informations de copyright
Copyright © 2023 Termedia.
Déclaration de conflit d'intérêts
The authors declare no conflict of interest.
Références
Pathol Res Pract. 2019 Dec;215(12):152700
pubmed: 31704149
J Oral Pathol Med. 2013 Feb;42(2):166-73
pubmed: 22650413
J Immunol. 2008 Dec 1;181(11):7660-9
pubmed: 19017954
Int J Mol Sci. 2020 Dec 29;22(1):
pubmed: 33383632
Nat Commun. 2021 Feb 5;12(1):832
pubmed: 33547304
Scand J Immunol. 2007 Aug-Sep;66(2-3):143-58
pubmed: 17635792
Int J Mol Sci. 2018 Mar 24;19(4):
pubmed: 29587347
Int J Mol Med. 2005 Aug;16(2):269-73
pubmed: 16012760
Sci Rep. 2019 Jul 23;9(1):10677
pubmed: 31337865
Biochim Biophys Acta. 2013 Aug;1836(1):177-85
pubmed: 23648450
J Diabetes Res. 2020 Oct 15;2020:2583257
pubmed: 33123595
Immunity. 2016 May 17;44(5):989-1004
pubmed: 27192565
J Neuropathol Exp Neurol. 2021 Jun 4;80(6):541-551
pubmed: 33990845
Asian Pac J Cancer Prev. 2014;15(5):2145-52
pubmed: 24716948
Cancer Sci. 2020 Jun;111(6):1943-1957
pubmed: 32304268
BMC Nephrol. 2013 Jan 22;14:23
pubmed: 23339460
J Immunother Cancer. 2020 Oct;8(2):
pubmed: 33082168
J Otolaryngol Head Neck Surg. 2013 Apr 19;42:30
pubmed: 23672952
Lung Cancer. 2019 Oct;136:80-85
pubmed: 31454748
Clin Cancer Res. 2000 Dec;6(12):4635-40
pubmed: 11156213
Clin Immunol. 2007 Aug;124(2):221-33
pubmed: 17560833
Int J Mol Sci. 2018 Feb 01;19(2):
pubmed: 29389859