Department of Oral and Maxillofacial Surgery, Friedrich-Alexander University Erlangen-Nürnberg, Glueckstrasse 11, 91054, Erlangen, Germany.
Department of Nephropathology, Institute of Pathology, Friedrich-Alexander University Erlangen-Nürnberg, Erlangen, Germany.
BMC Cancer. 2018 Aug 16;18(1):823. doi: 10.1186/s12885-018-4726-6.
Neck dissection is standard in surgical management of oral squamous cell carcinomas (oscc). However, the immunologic link between primary tumor and lymph nodes is insufficiently understood. Galectin 3 (Gal3) promotes M2 polarization of macrophages and contributes to immunosuppression. The current study analyzes the association between Gal3 expression in regional lymph nodes of oscc with histomorphologic parameters (T-, N-, L- Pn-stage, grading) of the primary tumor. Additionally, Gal3 expression is correlated with markers of macrophage polarization (M1 vs. M2).
Preoperative diagnostic biopsies (n = 26), tumor resection specimens (n = 34), tumor-free lymph nodes (n = 28) and lymph node metastases (n = 10) of T1/T2 oscc patients were immunohistochemically analyzed for Gal3 and macrophage marker (CD68, CD11c, CD163 and MRC1) expression. The number of positive cells and the expression ratios were quantitatively assessed.
High Gal3 expression in tumor-free regional lymph nodes was significantly (p < 0.05) associated with increased tumor size. The epithelial compartment of lymph node metastases showed a significantly (p < 0.05) increased Gal3 expression compared to biopsies and tumor resection specimens. Cell density of M2 macrophages was significantly (p < 0.05) and positively correlated with the number of Gal3 expressing cells in lymph nodes and tumor specimens.
Gal3 expression in regional lymph nodes might be associated with oscc progression. The increased Gal3 expression in regional lymph nodes of larger tumors underlines the need of immunomodulatory treatment concepts in early-stage oscc. Blocking of Gal3 might be a therapeutic option in oral cancer.
颈清扫术是口腔鳞状细胞癌(OSCC)手术治疗的标准方法。然而,原发肿瘤与淋巴结之间的免疫联系尚未得到充分理解。半乳糖凝集素 3(Gal3)促进巨噬细胞 M2 极化,并有助于免疫抑制。本研究分析了 OSCC 区域淋巴结中 Gal3 表达与原发肿瘤组织学形态参数(T、N、L、Pn 分期、分级)之间的关系。此外,Gal3 表达与巨噬细胞极化标志物(M1 与 M2)相关。
对 T1/T2 OSCC 患者的术前诊断性活检(n=26)、肿瘤切除标本(n=34)、肿瘤无转移淋巴结(n=28)和淋巴结转移(n=10)进行免疫组织化学分析,检测 Gal3 和巨噬细胞标志物(CD68、CD11c、CD163 和 MRC1)的表达。定量评估阳性细胞数和表达比。
肿瘤无转移淋巴结中 Gal3 高表达与肿瘤大小增加显著相关(p<0.05)。与活检和肿瘤切除标本相比,淋巴结转移的上皮细胞区 Gal3 表达显著增加(p<0.05)。淋巴结和肿瘤标本中 Gal3 表达细胞的数量与 M2 巨噬细胞的细胞密度呈显著正相关(p<0.05)。
区域淋巴结中的 Gal3 表达可能与 OSCC 进展相关。较大肿瘤区域淋巴结中 Gal3 表达的增加强调了早期 OSCC 中免疫调节治疗概念的必要性。Gal3 阻断可能是口腔癌的一种治疗选择。