Department of Pathology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Department of Ophthalmology, Leiden University Medical Center, Leiden, The Netherlands.
Invest Ophthalmol Vis Sci. 2019 Jul 1;60(8):2950-2957. doi: 10.1167/iovs.19-27162.
Chemokines play a role in the progression and metastatic spread of both cutaneous and uveal melanomas. The aim of this study was to examine the prognostic value of expression of chemokine receptors CCR7, CXCR4, and CCR10 in conjunctival melanocytic lesions.
In total, 44 conjunctival nevi, 21 cases of primary acquired melanosis (PAM) with atypia and 35 conjunctival melanomas, were included. After immunohistochemical staining for CCR7, CXCR4, and CCR10 the immunoreactive score (IRS) was determined. The findings were correlated for association with melanoma and development of metastasis. For mechanistic evaluation, we used a mouse melanoma metastasis model using two human conjunctival melanoma cell lines, CM2005.1 and CRMM1.
All tested chemokines showed a significantly higher expression in conjunctival melanoma than conjunctival nevi. There was a statistically significant difference between the IRS in nevi and PAM with atypia for nuclear IRS in CCR10 (P = 0.03) and both nuclear and cytoplasmic IRS in CXCR4 (P < 0.01 and P = 0.03, respectively); this was also true evaluating the groups PAM with atypia and melanoma all together (P < 0.01). Furthermore, a trend for lower IRS was seen in cases of melanoma without metastasis, with a suggestive pattern of a higher IRS in cases that did develop metastases, supported for CXCR4 using the mouse melanoma metastasis model.
Expression of specific chemokines changes during the progression and metastatic spread of conjunctival melanocytic lesions. Differential chemokine profiles may hold prognostic value for patients with conjunctival melanomas and might be considered as a therapeutic target.
趋化因子在皮肤和葡萄膜黑色素瘤的进展和转移扩散中发挥作用。本研究旨在探讨趋化因子受体 CCR7、CXCR4 和 CCR10 在结膜黑色素细胞病变中的表达的预后价值。
共纳入 44 例结膜痣、21 例伴不典型性的原发性获得性黑色素沉着(PAM)和 35 例结膜黑色素瘤。用免疫组化法检测 CCR7、CXCR4 和 CCR10 的表达,确定免疫反应评分(IRS)。将这些发现与黑色素瘤和转移的发生相关联。为了进行机制评估,我们使用了两种人结膜黑色素瘤细胞系 CM2005.1 和 CRMM1 的小鼠黑色素瘤转移模型。
所有检测的趋化因子在结膜黑色素瘤中的表达均明显高于结膜痣。CCR10 的核 IRS(P = 0.03)和 CXCR4 的核和细胞质 IRS(P < 0.01 和 P = 0.03,分别)在痣和伴不典型性的 PAM 之间的 IRS 存在统计学显著差异;评估伴不典型性的 PAM 和黑色素瘤的所有组之间也是如此(P < 0.01)。此外,在无转移的黑色素瘤病例中 IRS 较低,而在发生转移的病例中 IRS 较高,这一趋势在使用小鼠黑色素瘤转移模型评估 CXCR4 时得到了支持。
在结膜黑色素细胞病变的进展和转移扩散过程中,特定趋化因子的表达发生变化。差异的趋化因子谱可能对结膜黑色素瘤患者具有预后价值,并可作为治疗靶点。