Loading…

Prognostic effect of programmed cell death ligand 1/programmed cell death 1 expression in cancer stem cells of human oral squamous cell carcinoma

The relationship between cancer stem cells (CSCs) in oral squamous cell carcinoma (OSCC) and programmed cell death ligand 1 (PD-Ll)/programmed cell death 1 (PD-1) remains unclear. Therefore, the present study aimed to clarify the association between the [CD44v3.sup.high]/[CD24.sup.low] immunophenoty...

Full description

Saved in:
Bibliographic Details
Published in:Oncology letters 2024-02, Vol.27 (2), p.1, Article 79
Main Authors: Todoroki, Keita, Abe, Yushi, Matsuo, Katsuhisa, Nomura, Hidetosi, Kawahara, Akihiko, Nakamura, Yoshiaki, Nakamura, Moriyoshi, Seki, Naoko, Kusukawa, Jingo
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:The relationship between cancer stem cells (CSCs) in oral squamous cell carcinoma (OSCC) and programmed cell death ligand 1 (PD-Ll)/programmed cell death 1 (PD-1) remains unclear. Therefore, the present study aimed to clarify the association between the [CD44v3.sup.high]/[CD24.sup.low] immunophenotype of CSCs in OSCC and PD-L1/PD-1 co-expression, and to assess the prognostic effect of CSCs in terms of immune checkpoint molecules. Formalin-fixed, paraffin-embedded tissue samples and clinicopathological data from 168 patients with OSCC were retrospectively retrieved. Immunohistochemical staining and reverse transcription quantitative polymerase chain reaction were applied to a tissue microarray of the invasive front of each case. Semi-automated cell counting was used to assess CD44v3, CD24, PD-L1 and PD-1 expression by immunohistochemistry (IHC) using a digital image analysis program. Associations between immunological markers and clinicopathological variables were estimated. Patients with the CSC immunophenotype [CD44v3.sup.high]/[CD24.sup.low], and patients with a high PD-L1/PD-1-positive cell density in the tumor parenchyma and stroma had significantly lower survival rates. Furthermore, patients with the CSC immunophenotype ([CD44v3.sup.high]/[CD24.sup.low]) and high PD-L1/PD-1 co-expression had even lower survival rates (P
ISSN:1792-1074
1792-1082
DOI:10.3892/ol.2024.14213