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血管内皮生长因子 C/D 的表达和淋巴管密度均不能支持局部复发多形性腺瘤局部扩散的机制是淋巴浸润。

Neither expression of VEGF-C/D nor lymph vessel density supports lymphatic invasion as the mechanism responsible for local spread of recurrent salivary pleomorphic adenoma.

出版信息

Virchows Arch. 2014 Jan;464(1):29-34. doi: 10.1007/s00428-013-1502-5.

DOI:10.1007/s00428-013-1502-5
PMID:24233153
Abstract

Recent research suggests that multinodular recurrent pleomorphic adenoma (PA) might result from cell migration through lymphatics. Lymphangiogenesis in malignancies is mediated by vascular endothelial growth factors C and D (VEGF-C/D). We studied the expression of VEGF-C/D in PA by immunohistochemistry as well as lymphatic vessel density (LVD). In 6 non-recurrent, 4 primary-to-recur, and 10 recurrent PAs, VEGF-C/D expression was assessed by immunohistochemistry. Staining was scored in terms of staining intensity (0 = absent to 3 = strong), and the percentage of positive tumor cells (scored as 0 (0-19 %), 1 (20-39 %), 2 (40-50 %), and 3 (60-100 %)) and a sum score were calculated. Intra- and peritumoral LVD was assessed by counting of LV after immunostaining, using the D2-40 antibody. All but one sample were VEGF-C negative. The differences in VEGF-D expression between non-recurrent, primary-to-recur, and recurrent PAs were not significant (p>0.05). VEGF-D expression did not correlate with peritumoral LVD (p>0.05). Our study revealed a significant difference between intra- and peritumoral LVD values when comparing individual and all sample groups (p=0.01). The lack of VEGF-C expression and of significant differences in VEGF-D expression and peritumoral LVD between patients with non-recurrent, primary-to-recur, and recurrent PAs does not support the lymphangiogenic local spread hypothesis

摘要

最近的研究表明,多结节复发性多形性腺瘤(PA)可能是由于细胞通过淋巴管迁移而导致的。恶性肿瘤中的淋巴管生成是由血管内皮生长因子 C 和 D(VEGF-C/D)介导的。我们通过免疫组织化学研究了 PA 中 VEGF-C/D 的表达以及淋巴管密度(LVD)。在 6 例非复发性、4 例原发性复发和 10 例复发性 PA 中,通过免疫组织化学评估了 VEGF-C/D 的表达。根据染色强度(0=无到 3=强)和阳性肿瘤细胞的百分比(评分 0(0-19%)、1(20-39%)、2(40-50%)和 3(60-100%))和总和评分进行评分。使用 D2-40 抗体进行免疫染色后,通过计数 LV 评估肿瘤内和肿瘤周围的 LVD。除一个样本外,所有样本均为 VEGF-C 阴性。非复发性、原发性复发和复发性 PA 之间 VEGF-D 表达的差异无统计学意义(p>0.05)。VEGF-D 表达与肿瘤周围 LVD 无相关性(p>0.05)。当比较个体和所有样本组时,我们发现肿瘤内和肿瘤周围 LVD 值之间存在显著差异(p=0.01)。缺乏 VEGF-C 表达以及非复发性、原发性复发和复发性 PA 患者之间 VEGF-D 表达和肿瘤周围 LVD 无显著差异,这并不支持淋巴管生成的局部扩散假说。

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