Współczesna Onkologia

Abstract

1/2023 vol. 27
Original paper

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

  1. Department of Pathomorphology, Medical University of Gdansk, Gdansk, Poland
  2. Department of Oncology, Institute of Medical Sciences, University of Opole, Opole, Poland
  3. Division of Radiotherapy, IEO European Institute of Oncology, IRCCS, Milan, Italy
  4. Department of Oral Surgery, Medical University of Gdansk, Gdansk, Poland
Contemp Oncol (Pozn) 2023; 27 (1): 22–27
Online publish date: 2023/04/27
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Introduction

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).

Material and methods

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.

Results

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 (p = 0.029).

Conclusions

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.

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