1] Inserm UMR1037, Equipe Labellisée Ligue Contre le Cancer 2013, Centre de Recherches en Cancérologie de Toulouse, Toulouse, France [2] Université Toulouse III Paul-Sabatier, Toulouse, France.
Institute of Pharmacology, University of Bern, Bern, Switzerland.
Oncogene. 2014 Jun 26;33(26):3364-73. doi: 10.1038/onc.2013.303. Epub 2013 Jul 29.
Despite progress in the understanding of the biology and genetics of melanoma, no effective treatment against this cancer is available. The adjacent microenvironment has an important role in melanoma progression. Defining the molecular signals that control the bidirectional dialog between malignant cells and the surrounding stroma is crucial for efficient targeted therapy. Our study aimed at defining the role of sphingosine-1-phosphate (S1P) in melanoma-stroma interactions. Transcriptomic analysis of human melanoma cell lines showed increased expression of sphingosine kinase-1 (SPHK1), the enzyme that produces S1P, as compared with normal melanocytes. Such an increase was also observed by immunohistochemistry in melanoma specimens as compared with nevi, and occurred downstream of ERK activation because of BRAF or NRAS mutations. Importantly, migration of melanoma cells was not affected by changes in SPHK1 activity in tumor cells, but was stimulated by comparable modifications of S1P-metabolizing enzymes in cocultured dermal fibroblasts. Reciprocally, incubation of fibroblasts with the conditioned medium from SPHK1-expressing melanoma cells resulted in their differentiation to myofibroblasts, increased production of matrix metalloproteinases and enhanced SPHK1 expression and activity. In vivo tumorigenesis experiments showed that the lack of S1P in the microenvironment prevented the development of orthotopically injected melanoma cells. Finally, local tumor growth and dissemination were enhanced more efficiently by coinjection of wild-type skin fibroblasts than by fibroblasts from Sphk1(-/-) mice. This report is the first to document that SPHK1/S1P modulates the communication between melanoma cells and dermal fibroblasts. Altogether, our findings highlight SPHK1 as a potential therapeutic target in melanoma progression.
尽管人们在理解黑色素瘤的生物学和遗传学方面取得了进展,但针对这种癌症仍没有有效的治疗方法。相邻的微环境在黑色素瘤的进展中起着重要作用。定义控制恶性细胞与周围基质之间双向对话的分子信号对于有效的靶向治疗至关重要。我们的研究旨在定义鞘氨醇-1-磷酸(S1P)在黑色素瘤-基质相互作用中的作用。与正常黑素细胞相比,人类黑色素瘤细胞系的转录组分析显示鞘氨醇激酶-1(SPHK1)的表达增加,SPHK1 是产生 S1P 的酶。与痣相比,在黑色素瘤标本中通过免疫组织化学也观察到这种增加,并且由于 BRAF 或 NRAS 突变而发生在 ERK 激活的下游。重要的是,黑色素瘤细胞的迁移不受肿瘤细胞中 SPHK1 活性变化的影响,但受到共培养真皮成纤维细胞中 S1P 代谢酶可比修饰的刺激。反过来,用表达 SPHK1 的黑色素瘤细胞的条件培养基孵育成纤维细胞会导致其分化为肌成纤维细胞,增加基质金属蛋白酶的产生并增强 SPHK1 的表达和活性。体内肿瘤发生实验表明,微环境中 S1P 的缺乏可阻止原位注射的黑色素瘤细胞的发展。最后,与从 Sphk1(-/-) 小鼠中分离的成纤维细胞相比,野生型皮肤成纤维细胞的共注射更有效地增强了局部肿瘤的生长和扩散。本报告首次证明 SPHK1/S1P 调节黑色素瘤细胞和真皮成纤维细胞之间的通讯。总之,我们的研究结果强调了 SPHK1 作为黑色素瘤进展中潜在的治疗靶点。