Department of Biochemistry, Universidad Autónoma de Madrid (UAM) and Instituto de Investigaciones Biomédicas Alberto Sols, CSIC-UAM, Madrid, Spain.
Melanoma Res. 2011 Aug;21(4):285-97. doi: 10.1097/CMR.0b013e32834495c3.
Pigment epithelium-derived factor (PEDF) is a broad-spectrum angiogenesis inhibitor that displays potent antimetastatic activity in multiple tumor types. We have previously shown that PEDF prevents primary tumor growth and metastatic spread of human melanoma in mouse experimental models. Consistent with these observations, PEDF expression is lost at the late stages of melanoma progression, allowing melanoma cells to become angiogenic, migratory, and invasive. PEDF's ability to modify the interplay between the host and tumor tissues strongly supports its use as a therapeutic agent for the treatment of metastatic melanoma. However, transition to the clinic requires a more detailed knowledge of the molecular mechanisms underpinning PEDF's activity. In this study, we describe changes in the gene expression profile of A375 human melanoma cells induced by PEDF overexpression. PEDF modulated diverse categories of genes known to be involved in angiogenesis and migration. It downregulated cytokines such as interleukin-8 and extracellular matrix proteins such as collagen IV, while it upregulated fibronectin. Multiple transcripts previously described as contributing to the acquisition of malignant phenotype by melanoma were also diminished by PEDF overexpression, among which we validated galectin 3 and jagged 1. In addition, PEDF downregulated S100β and melanoma inhibitory activity, which are widely used in the pathological diagnosis of melanoma. Interestingly, PEDF increased the expression of melanophilin and decreased rab27A, which are relevant targets for melanosome transport; suggesting that PEDF could directly impinge on melanocytic lineage-specific processes. Our study identifies new molecular targets and signaling pathways that may potentially contribute to determine PEDF's ability to restrict the aggressiveness of A375 human melanoma cells.
色素上皮衍生因子(PEDF)是一种广谱血管生成抑制剂,在多种肿瘤类型中显示出强大的抗转移活性。我们之前已经表明,PEDF 可防止人黑色素瘤在小鼠实验模型中的原发性肿瘤生长和转移扩散。与这些观察结果一致,PEDF 的表达在黑色素瘤进展的晚期丢失,从而使黑色素瘤细胞变得血管生成、迁移和侵袭。PEDF 改变宿主和肿瘤组织之间相互作用的能力强烈支持将其用作治疗转移性黑色素瘤的治疗剂。然而,向临床的转变需要更详细地了解支撑 PEDF 活性的分子机制。在这项研究中,我们描述了 A375 人黑色素瘤细胞中由 PEDF 过表达诱导的基因表达谱的变化。PEDF 调节了已知参与血管生成和迁移的多种基因类别。它下调了白细胞介素 8 等细胞因子和胶原蛋白 IV 等细胞外基质蛋白,同时上调了纤维连接蛋白。PEDF 过表达还下调了先前被描述为有助于黑色素瘤获得恶性表型的多个转录本,其中我们验证了半乳糖凝集素 3 和 jagged 1。此外,PEDF 下调了 S100β 和黑色素抑制活性,这些广泛用于黑色素瘤的病理诊断。有趣的是,PEDF 增加了黑素小体运输相关的黑素体磷蛋白的表达并降低了 rab27A 的表达;表明 PEDF 可能直接影响黑素细胞谱系特异性过程。我们的研究确定了新的分子靶标和信号通路,这些靶标和信号通路可能有助于确定 PEDF 限制 A375 人黑色素瘤细胞侵袭性的能力。