Innoprot SL, Bizkaia Technology Park, Derio, Bizkaia, Spain.
Department of Cellular Biology and Histology, Basque Country University School of Medicine and Dentistry, Leioa, Bizkaia, Spain.
J Invest Dermatol. 2014 Feb;134(2):470-480. doi: 10.1038/jid.2013.342. Epub 2013 Aug 12.
Very late antigen-4 (VLA-4) is frequently overexpressed on melanoma cells contributing to inflammation-dependent metastasis. Melanoma cell adhesion to endothelium via VLA-4-vascular cell adhesion molecule-1 (VCAM-1) interaction was used to study VLA-4 activation during melanoma cell response to inflammation. Cooperation among major inflammatory mediators was analyzed in melanoma cells exposed to single inflammatory factors in the presence of inhibitors for other assayed mediators. A stepwise cascade of hierarchized molecules heterogeneously made and used during melanoma response to IL-18, induced hydrogen peroxide (H2O2), in turn activating VLA-4 and melanoma cell adhesion to endothelium. The cascade involved prostaglandin E2 (PGE2) production from melanoma induced by IL-18-dependent tumor necrosis factor-α (TNFα); next, PGE2-induced IL-1β via vascular endothelial growth factor (VEGF) secretion, which in turn induced VLA-4 activation via cyclooxygenase 2-dependent H2O2. This sequence operated in IL-18R/VLA-4/VEGF-expressing murine (B16) and human (A375 and 883) melanomas, but not in those without this phenotype. Separation of active VLA-4-expressing B16 melanoma cells through immobilized VCAM-1 verified their higher IL-18R/TNFR1/VEGFR2 expression and metastatic growth than inactive VLA-4-expressing cells. However, cooperation among melanoma cell sub-populations with heterogeneous cytokine receptor levels may occur through VLA-4-stimulating factors, leading to intratumoral amplification of metastatic potential. Therefore, expression of the VLA-4-stimulating factor sequence may help to predict melanoma prometastatic risk, and offers therapeutic targets for metastatic melanoma deactivation through VLA-4 activation blockade.
非常晚期抗原-4(VLA-4)在黑色素瘤细胞中经常过度表达,有助于炎症依赖性转移。通过 VLA-4-血管细胞黏附分子-1(VCAM-1)相互作用,黑色素瘤细胞黏附在内皮细胞上,用于研究黑色素瘤细胞对炎症反应过程中 VLA-4 的激活。分析了在存在其他测定的介质抑制剂的情况下,暴露于单一炎症因子的黑色素瘤细胞中主要炎症介质之间的合作。在 IL-18 诱导的过氧化氢(H2O2)的情况下,黑色素瘤对 IL-18 的反应中逐步级联的分层分子不均匀地产生和使用,依次激活 VLA-4 和黑色素瘤细胞与内皮细胞的黏附。级联反应涉及由 IL-18 依赖性肿瘤坏死因子-α(TNFα)诱导的黑色素瘤产生的前列腺素 E2(PGE2);接下来,PGE2 通过血管内皮生长因子(VEGF)分泌诱导 IL-1β,反过来通过环氧化酶 2 依赖性 H2O2 诱导 VLA-4 激活。这个序列在表达 IL-18R/VLA-4/VEGF 的鼠(B16)和人(A375 和 883)黑色素瘤中起作用,但在没有这种表型的黑色素瘤中不起作用。通过固定化 VCAM-1 分离活性 VLA-4 表达的 B16 黑色素瘤细胞,证实它们比非活性 VLA-4 表达细胞具有更高的 IL-18R/TNFR1/VEGFR2 表达和转移性生长。然而,通过 VLA-4 刺激因子,具有不同细胞因子受体水平的黑色素瘤细胞亚群之间可能发生合作,导致肿瘤内转移潜力的扩增。因此,VLA-4 刺激因子序列的表达可能有助于预测黑色素瘤的促转移风险,并为通过 VLA-4 激活阻断来治疗转移性黑色素瘤提供治疗靶点。