Expression of Putative Cancer Stem Cell Markers in Oral Squamous Cell Carcinoma: Correlation with Clinicopathological Features

Oral squamous cell carcinoma (OSCC) is an aggressive epithelial malignancy with high local invasiveness and a tendency for early cervical lymph node metastasis. Conventional prognostic markers often lack precision. This study evaluated the expression of putative cancer stem cell markers-CD44, CD133, and CD166-in OSCC tissues and explored their associations with clinical parameters, including salivary flow rates. Twelve patients with histologically confirmed OSCC (9 males, 3 females; mean age: 65 years) were included. Clinical TNM staging and tumor dimensions were recorded. Depth of invasion was measured histologically. Tumor tissues were enzymatically dissociated to establish primary cell cultures, and flow cytometry was used to quantify putative cancer stem cell markers expression. Unstimulated salivary flow rates were measured using sialometry. CD44 expression was uniformly high (median: 96.4%) and CD166 showed moderate to high expression (median: 85.5%), while CD133 was low (median: 1.5%). Co-expression levels were the highest for CD44+/CD166+ (median: 86.6%). Triple-marker co-expression had a median of 2.0%. Depth of invasion was positively correlated with CD133+ and its co-expression with CD44+ and CD166+ (<i>p</i> ≤ 0.05). Salivary flow rates were negatively correlated with CD166+ and CD44+/CD166+ expression (<i>p</i> ≤ 0.01). These findings suggest putative cancer stem cell markers, particularly CD133, may have prognostic value in OSCC and warrant further investigation.

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Journal
International Journal of Molecular Sciences
Published
2025-11-12
DOI
https://doi.org/10.3390/ijms262210939
Primary Topic
Cancer Cells and Metastasis
Type
article
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article

Expression of Putative Cancer Stem Cell Markers in Oral Squamous Cell Carcinoma: Correlation with Clinicopathological Features

Diana Bugarski, Aleksandra Jauković, Miroslav Ilić, Biljana Pokimica et al.
International Journal of Molecular Sciences
Cancer Cells and Metastasis
article

Expression of Putative Cancer Stem Cell Markers in Oral Squamous Cell Carcinoma: Correlation with Clinicopathological Features

Diana Bugarski, Aleksandra Jauković, Miroslav Ilić, Biljana Pokimica, Slavko Mojsilović, Anđelija Petrović
article en

Abstract

Oral squamous cell carcinoma (OSCC) is an aggressive epithelial malignancy with high local invasiveness and a tendency for early cervical lymph node metastasis. Conventional prognostic markers often lack precision. This study evaluated the expression of putative cancer stem cell markers-CD44, CD133, and CD166-in OSCC tissues and explored their associations with clinical parameters, including salivary flow rates. Twelve patients with histologically confirmed OSCC (9 males, 3 females; mean age: 65 years) were included. Clinical TNM staging and tumor dimensions were recorded. Depth of invasion was measured histologically. Tumor tissues were enzymatically dissociated to establish primary cell cultures, and flow cytometry was used to quantify putative cancer stem cell markers expression. Unstimulated salivary flow rates were measured using sialometry. CD44 expression was uniformly high (median: 96.4%) and CD166 showed moderate to high expression (median: 85.5%), while CD133 was low (median: 1.5%). Co-expression levels were the highest for CD44+/CD166+ (median: 86.6%). Triple-marker co-expression had a median of 2.0%. Depth of invasion was positively correlated with CD133+ and its co-expression with CD44+ and CD166+ (<i>p</i> ≤ 0.05). Salivary flow rates were negatively correlated with CD166+ and CD44+/CD166+ expression (<i>p</i> ≤ 0.01). These findings suggest putative cancer stem cell markers, particularly CD133, may have prognostic value in OSCC and warrant further investigation.

International Journal of Molecular SciencesVol. 26(22)
University of Novi Sad (RS), Klinički centar Vojvodine (RS), University of Belgrade (RS), Centre of Research Excellence in Nutrition and Metabolism (RS)
Openalex Percentile: Top 54%
Cancer Cells and Metastasis
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