Voelker Hans-Ullrich, Hintermeier Isabelle, Strehl Annette, Scheich Matthias
Department of Pathology, Leopoldina Krankenhaus GmbH, Gustav-Adolf-Str. 8, D-97422 Schweinfurt, Germany.
Department of Oto-Rhino-Laryngology, Plastic, Aesthetic and Reconstructive Head and Neck Surgery, University Hospital of Wuerzburg, Josef-Schneider-Str. 2, D-97080 Wuerzburg, Germany.
World J Oncol. 2020 Apr;11(2):65-71. doi: 10.14740/wjon1259. Epub 2020 Mar 29.
Podoplanin (D2-20) stains immunohistochemically lymphatic vessels, regular mesothelium and tumor cells of different tumors, e.g. malignant mesothelioma or seminoma. In squamous cell carcinoma (SCC), the marker has been described as variously expressed.
This study has investigated the value of the immunohistochemical analysis for the prognostic relevance of the expression in 119 SCCs of the larynx and hypopharynx. The clinical data and documentation of follow-up for at least 5 years were available.
The collective showed the expected distribution of patient age with accentuation of the male sex and a balanced spread of tumor stages including nodal status. The immunohistochemical stain intensity (negative, weak or strong) and the distribution (equal versus focal) were evaluated. In addition, the accentuation of the staining reaction was separately examined at the border of invasion. SCCs with a strong expression of podoplanin were associated with an unfavorable prognosis. A comparison of grouped cases showed a trend emerging with borderline results (negative to weakly positive, P = 0.51; negative to strongly positive, P = 0.054; weakly positive to strongly positive, P = 0.17). The staining at the border of invasion had no statistical effect on overall survival. Multivariate survival statistics however showed that lymphonodal metastasis and a reaction with podoplanin in tumor cells are associated with significant worse prognosis.
In summary, regardless of the exact function of podoplanin in the process of cell migration and tumor progression, an immunohistochemical identification of expression in tumor cells of SCC of the larynx and hypopharynx can give additional information about the expectable prognosis.
血小板内皮细胞黏附分子(D2-20)可通过免疫组织化学方法标记淋巴管、正常间皮以及不同肿瘤(如恶性间皮瘤或精原细胞瘤)的肿瘤细胞。在鳞状细胞癌(SCC)中,该标志物的表达情况各异。
本研究调查了免疫组织化学分析在119例喉和下咽鳞状细胞癌中表达的预后相关性价值。研究获取了临床数据以及至少5年的随访记录。
该组患者呈现出预期的年龄分布,男性居多,肿瘤分期(包括淋巴结状态)分布均衡。评估了免疫组织化学染色强度(阴性、弱阳性或强阳性)以及分布情况(均匀分布与局灶分布)。此外,还单独检查了侵袭边界处染色反应的增强情况。血小板内皮细胞黏附分子强表达的鳞状细胞癌预后不良。分组病例比较显示出一种趋势,结果接近临界值(阴性至弱阳性,P = 0.51;阴性至强阳性,P = 0.054;弱阳性至强阳性,P = 0.17)。侵袭边界处的染色对总生存期无统计学影响。然而,多变量生存统计显示,淋巴结转移以及肿瘤细胞中血小板内皮细胞黏附分子的反应与显著更差的预后相关。
总之,无论血小板内皮细胞黏附分子在细胞迁移和肿瘤进展过程中的具体功能如何,对喉和下咽鳞状细胞癌肿瘤细胞中该分子表达进行免疫组织化学鉴定可为预期预后提供额外信息。