Department of Oral and Maxillofacial Surgery, Capital Medical University School of Stomatology, Capital Medical University, Beijing, China.
Department of Stomatology, Beijing Jishuitan Hospital, Beijing, China.
Neoplasma. 2020 May;67(3):700-706. doi: 10.4149/neo_2020_190821N802. Epub 2020 Mar 24.
Oral squamous cell carcinoma (OSCC) presents severe morbidity and high mortality owing to local recurrence or remote metastasis. Molecular markers, including chemokines, might provide more efficient prognostic information or even therapeutic targets for the treatment of OSCC. Using quantitative RT-qPCR, we found that CCL18 was dramatically overexpressed in 30 OSCC tissues at the mRNA level in comparison with their adjacent non-cancerous oral mucosa tissues and 15 oral mucosa tissues from non-malignant patients. We then analyzed the relationship between CCL18 overexpression and patient clinical characters and outcomes using immunohistochemistry staining (IHC) in 102 paired OSCC cancerous and adjacent non-cancerous tissues; the increase in CCL18 expression was significantly higher in male patients (p=0.047), tumors of the palate and floor of the mouth (p=0.014), patients with positive lymph node metastasis (p=0.007), and patients with poor tumor differentiation (p=0.029). The median overall survival time and time-to-recurrence were 80.6 and 61.4 months in patients with high CCL18 expression, respectively, as against 93.4 and 81.6 months in patients with comparatively lower CCL18 expression, respectively (p=0.033 and 0.012, respectively; log-rank test). Multivariate analyses indicated age, poor differentiation, and CCL18 levels to be independent prognostic factors for predicting both overall and disease-free survival time. Our study suggests that CCL18 is a novel candidate marker for the OSCC malignancy and prognosis, including lymph node metastasis, time-to-recurrence, and disease-free survival time.
口腔鳞状细胞癌(OSCC)由于局部复发或远处转移,导致发病率高且死亡率高。包括趋化因子在内的分子标志物可能为 OSCC 的治疗提供更有效的预后信息甚至治疗靶点。通过定量 RT-qPCR,我们发现与相邻非癌性口腔黏膜组织和 15 名非恶性患者的口腔黏膜组织相比,30 例 OSCC 组织中 CCL18 的 mRNA 水平显著上调。然后,我们通过对 102 对配对的 OSCC 癌性和相邻非癌性组织的免疫组织化学染色(IHC)分析 CCL18 过表达与患者临床特征和结局之间的关系;男性患者(p=0.047)、腭部和口底肿瘤(p=0.014)、阳性淋巴结转移患者(p=0.007)和肿瘤分化不良患者(p=0.029)中 CCL18 表达增加更为显著。高 CCL18 表达患者的中位总生存时间和复发时间分别为 80.6 和 61.4 个月,而 CCL18 表达较低的患者分别为 93.4 和 81.6 个月(p=0.033 和 0.012,log-rank 检验)。多因素分析表明年龄、分化不良和 CCL18 水平是预测总生存时间和无病生存时间的独立预后因素。我们的研究表明 CCL18 是 OSCC 恶性肿瘤和预后的一个新的候选标志物,包括淋巴结转移、复发时间和无病生存时间。