Department of Stomathology (Oral Pathology), School of Dentistry, Federal University of Goiás, Goiânia, Brazil.
Laboratory of Pathology, Araújo Jorge Hospital, Association of Cancer Combat of Goiás, Goiânia, Brazil.
J Oral Pathol Med. 2018 Oct;47(9):856-863. doi: 10.1111/jop.12762. Epub 2018 Jul 18.
Tumor-associated neutrophils (TAN), matrix metalloproteinase-9 (MMP-9), interleukin-17 (IL-17), and angiogenesis have been proposed as prognostic biomarkers of malignant tumors. The purpose of this study was to investigate these inflammatory markers as prognostic factors for oral squamous cell carcinoma (OSCC).
Specimens of OSCC (n = 30), healthy oral mucosa (negative control, n = 10), oral leukoplakia (n = 10), and apical granuloma with abscess (positive inflammatory controls, n = 10) were immunostained for CD66b (neutrophils), MMP-9, IL-17, and CD105 (neoformed microvessels). Semiquantitative (IL-17) and quantitative (CD66b, IL-17, MMP-9, and CD105) analyses were performed. Clinical information (TNM stage, metastasis, recurrence, and survival) and tumor histological grade were also obtained.
Positivity for TAN, MMP-9, IL-17, and CD105 was higher in OSCC than in the negative control (P < 0.05) and oral leukoplakia, but similar to the positive inflammatory control. Coincident high counts of inflammatory markers (CD66b, MMP-9, IL-17, and CD105) were associated with lymph node metastasis of OSCC. Associations between high numbers of neoformed microvessels and advanced clinical stage and a higher degree of malignancy were also demonstrated.
Combined positivity for TAN, MMP-9, IL-17, and CD105 appears to be associated with the metastasis-prone phenotype of OSCC.
肿瘤相关中性粒细胞(TAN)、基质金属蛋白酶-9(MMP-9)、白细胞介素-17(IL-17)和血管生成被认为是恶性肿瘤的预后生物标志物。本研究旨在探讨这些炎症标志物作为口腔鳞状细胞癌(OSCC)的预后因素。
免疫组化染色检测 30 例 OSCC 标本(病例组)、10 例健康口腔黏膜(阴性对照组)、10 例口腔白斑(口腔良性病变对照组)和 10 例根尖脓肿(阳性炎症对照组)的 CD66b(中性粒细胞)、MMP-9、IL-17 和 CD105(新生微血管)。进行半定量(IL-17)和定量(CD66b、IL-17、MMP-9 和 CD105)分析。同时获得临床信息(TNM 分期、转移、复发和生存)和肿瘤组织学分级。
与阴性对照组和口腔白斑相比,OSCC 中 TAN、MMP-9、IL-17 和 CD105 的阳性率更高(P<0.05),但与阳性炎症对照组相似。同时存在高计数的炎症标志物(CD66b、MMP-9、IL-17 和 CD105)与 OSCC 的淋巴结转移相关。新生微血管数量与晚期临床分期和更高的恶性程度之间也存在关联。
TAN、MMP-9、IL-17 和 CD105 的联合阳性似乎与 OSCC 的转移倾向表型相关。