Manchester Cancer Research Centre, Faculty of Biology, Medicine and Health, School of Medical Sciences, Division of Cancer Sciences, The University of Manchester, Michael Smith Building, Oxford Road, Manchester, M13 9PT, UK.
Oncogene. 2018 Jun;37(23):3166-3182. doi: 10.1038/s41388-018-0209-0. Epub 2018 Mar 16.
Despite the general focus on an invasive and de-differentiated phenotype as main driver of cancer metastasis, in melanoma patients many metastatic lesions display a high degree of pigmentation, indicative for a differentiated phenotype. Indeed, studies in mice and fish show that melanoma cells switch to a differentiated phenotype at secondary sites, possibly because in melanoma differentiation is closely linked to proliferation through the lineage-specific transcriptional master regulator MITF. Importantly, while a lot of effort has gone into identifying factors that induce the de-differentiated/invasive phenotype, it is not well understood how the switch to the differentiated/proliferative phenotype is controlled. We identify collagen as a contributor to this switch. We demonstrate that collagen stiffness induces melanoma differentiation through a YAP/PAX3/MITF axis and show that in melanoma patients increased collagen abundance correlates with nuclear YAP localization. However, the interrogation of large patient datasets revealed that in the context of the tumour microenvironment, YAP function is more complex. In the absence of fibroblasts, YAP/PAX3-mediated transcription prevails, but in the presence of fibroblasts tumour growth factor-β suppresses YAP/PAX3-mediated MITF expression and induces YAP/TEAD/SMAD-driven transcription and a de-differentiated phenotype. Intriguingly, while high collagen expression is correlated with poorer patient survival, the worst prognosis is seen in patients with high collagen expression, who also express MITF target genes such as the differentiation markers TRPM1, TYR and TYRP1, as well as CDK4. In summary, we reveal a distinct lineage-specific route of YAP signalling that contributes to the regulation of melanoma pigmentation and uncovers a set of potential biomarkers predictive for poor survival.
尽管人们普遍关注侵袭性和去分化表型作为癌症转移的主要驱动因素,但在黑色素瘤患者中,许多转移性病变显示出高度的色素沉着,表明其具有分化表型。事实上,在小鼠和鱼类中的研究表明,黑色素瘤细胞在次级部位向分化表型转换,这可能是因为在黑色素瘤中,分化与通过谱系特异性转录主调控因子 MITF 的增殖密切相关。重要的是,尽管已经投入大量精力来识别诱导去分化/侵袭表型的因素,但对于如何控制向分化/增殖表型的转换还了解甚少。我们发现胶原蛋白是这种转换的一个贡献因素。我们证明,胶原蛋白硬度通过 YAP/PAX3/MITF 轴诱导黑色素瘤分化,并表明在黑色素瘤患者中,胶原蛋白丰度增加与核 YAP 定位相关。然而,对大型患者数据集的分析表明,在肿瘤微环境的背景下,YAP 的功能更为复杂。在没有成纤维细胞的情况下,YAP/PAX3 介导的转录占主导地位,但在存在成纤维细胞的情况下,肿瘤生长因子-β抑制 YAP/PAX3 介导的 MITF 表达,并诱导 YAP/TEAD/SMAD 驱动的转录和去分化表型。有趣的是,尽管高胶原蛋白表达与患者生存率较差相关,但预后最差的是高胶原蛋白表达的患者,这些患者还表达 MITF 靶基因,如分化标志物 TRPM1、TYR 和 TYRP1,以及 CDK4。总之,我们揭示了 YAP 信号的一种独特的谱系特异性途径,该途径有助于黑色素瘤色素沉着的调节,并揭示了一组潜在的生物标志物,可预测不良预后。