de Lucena Morais Daniella, de Sena Luana Samara Balduíno, Silva Cunha John Lennon, de Mendonça Elismauro Francisco, Alves Pollianna Muniz, Nonaka Cassiano Francisco Weege
Department of Dentistry, State University of Paraíba, Campina Grande, PB, Brazil.
Department of Biological and Health Sciences, Federal University of Western Bahia, Barreiras, BA, Brazil.
Eur Arch Otorhinolaryngol. 2025 Apr;282(4):2105-2114. doi: 10.1007/s00405-024-09106-w. Epub 2024 Nov 29.
This study analyzed the immunoexpression of C-X-C chemokine ligand 12 (CXCL12) and C-X-C chemokine receptor 4 (CXCR4) in oral tongue squamous cell carcinoma (OTSCC) of young (≤ 45 years) and older (≥ 60 years) patients and correlated the findings with clinicopathological parameters (sex, tumor size, regional metastasis, clinical stage, and histopathological grade of malignancy).
Forty OTSCC cases (20 diagnosed in young patients and 20 diagnosed in older patients) were selected. Cytoplasmic (CXCL12 and CXCR4) and nuclear (CXCR4) staining percentages in epithelial and stromal cells were assessed at the invasive tumor front.
Low median percentages of CXCL12 positivity were observed in epithelial and stromal cells of OTSCC in both age groups. In stromal cells, expression of this chemokine was higher in older individuals compared to young individuals (p = 0.026). Expression of CXCR4 in neoplastic cells was more frequent in older individuals, with higher median percentages of cytoplasmic (p = 0.023) and nuclear (p = 0.001) positivity compared to young individuals. In stromal cells, older individuals exhibited a significantly higher cytoplasmic expression of CXCR4 (p < 0.001). No significant differences in CXCL12 or CXCR4 immunoexpression according to clinicopathological parameters was observed in either age group (p > 0.05). Positive correlations between cytoplasmic and nuclear expressions of CXCR4 were found in young (r = 0.580; p = 0.007) and older individuals (r = 0.476;p = 0.034).
The results suggest the participation of CXCR4 in the development of OTSCC, especially in older individuals. The findings also support possible age-related differences in the pathogenesis of this malignant neoplasm. Nevertheless, this protein may not be involved in the progression of OTSCC.
本研究分析了年轻(≤45岁)和老年(≥60岁)患者口腔舌鳞状细胞癌(OTSCC)中C-X-C趋化因子配体12(CXCL12)和C-X-C趋化因子受体4(CXCR4)的免疫表达情况,并将研究结果与临床病理参数(性别、肿瘤大小、区域转移、临床分期和组织病理学恶性分级)进行关联分析。
选取40例OTSCC病例(20例诊断为年轻患者,20例诊断为老年患者)。在肿瘤浸润前沿评估上皮细胞和基质细胞中的细胞质(CXCL12和CXCR4)及细胞核(CXCR4)染色百分比。
两个年龄组的OTSCC上皮细胞和基质细胞中CXCL12阳性的中位数百分比均较低。在基质细胞中,该趋化因子在老年个体中的表达高于年轻个体(p = 0.026)。CXCR4在肿瘤细胞中的表达在老年个体中更常见,与年轻个体相比,细胞质(p = 0.023)和细胞核(p = 0.001)阳性的中位数百分比更高。在基质细胞中,老年个体CXCR4的细胞质表达明显更高(p < 0.001)。在两个年龄组中,根据临床病理参数未观察到CXCL12或CXCR4免疫表达的显著差异(p > 0.05)。在年轻个体(r = 0.580;p = 0.007)和老年个体(r = 0.476;p = 0.034)中发现CXCR4的细胞质和细胞核表达之间呈正相关。
结果表明CXCR4参与了OTSCC的发生发展,尤其是在老年个体中。研究结果还支持了这种恶性肿瘤发病机制中可能存在的年龄相关差异。然而,这种蛋白可能不参与OTSCC的进展。