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血管内皮生长因子受体-3 表达预测原发性皮肤黑色素瘤前哨淋巴结状态。

Vascular Endothelial Growth Factor Receptor-3 Expression Predicts Sentinel Node Status in Primary Cutaneous Melanoma.

机构信息

Department of Dermatology, University Medical Center, Ruprecht-Karls-University Heidelberg, DE-69120 Heidelberg, Germany. E-mail:

出版信息

Acta Derm Venereol. 2020 Aug 18;100(15):adv00235. doi: 10.2340/00015555-3588.

Abstract

This study analysed the expression of vascular endothelial growth factor-A (VEGF), VEGFR-2, and VEGFR-3 in primary cutaneous melanomas with positive and negative sentinel node status (SLN) (a total of 58 specimens divided into 2 groups of 29 for each status). The specimens were collected from the pathological archive of the department of Dermatology, Venereology and Allergology of the University Medical Center Heidelberg. A quantification score was developed for protein expression, by considering the percentage of positive melanoma cells (0: 0%, 1: up to 1%, 2: 2-10%, 3: 11-50%, and 4: > 50%) in relation to the intensity of staining (0: negative, 1: low, 2: medium, 3: strong). Tumoural VEGFR-3 expression (mean ± standard deviation) in SLN+ tumours (9.62 ± 3.09) was significantly stronger than in SLN- tumours (6.13 ± 3.87; p < 0.001). A binary logistic regression model proved VEGFR-3 expression and tumour thickness to be significant independent predictors of SLN. These data provide evidence that VEGFR-3 expression may play a critical role in the pathogenesis of malignant melanoma and that its investigation may help to improve the selection of patients with primary cutaneous melanoma for sentinel node biopsy.

摘要

本研究分析了血管内皮生长因子-A(VEGF)、VEGFR-2 和 VEGFR-3 在原发性皮肤黑色素瘤中表达情况,这些黑色素瘤的前哨淋巴结(SLN)状态为阳性和阴性(共 58 个标本,分为 29 个阳性和 29 个阴性状态)。标本取自海德堡大学医学中心皮肤科、性病学和变态反应学部门的病理档案。通过考虑阳性黑色素瘤细胞的百分比(0:0%,1:≤1%,2:2-10%,3:11-50%,4:>50%)与染色强度(0:阴性,1:低,2:中,3:强)来制定蛋白表达的定量评分。在 SLN+肿瘤中,肿瘤 VEGFR-3 表达(平均值±标准差)(9.62±3.09)明显强于 SLN-肿瘤(6.13±3.87;p<0.001)。二元逻辑回归模型证明,VEGFR-3 表达和肿瘤厚度是 SLN 的显著独立预测因子。这些数据表明,VEGFR-3 表达可能在恶性黑色素瘤的发病机制中发挥关键作用,对其进行研究可能有助于改善对原发性皮肤黑色素瘤患者进行前哨淋巴结活检的选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a833/9207649/015911591427/ActaDV-100-15-5837-g001.jpg

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