Université de Lyon, F-69003, Lyon, France.
Université Lyon 1, Lyon, F-69003, France.
Oncogene. 2019 May;38(20):3781-3793. doi: 10.1038/s41388-019-0691-z. Epub 2019 Jan 24.
Due to its high proclivity to metastasize, and despite the recent development of targeted and immune therapy strategies, melanoma is still the deadliest form of skin cancer. Therefore, understanding the molecular mechanisms underlying melanoma invasion remains crucial. We previously characterized Tspan8 for its ability to prompt melanoma cell detachment from their microenvironment and trigger melanoma cell invasiveness, but the signaling events by which Tspan8 regulates the invasion process still remain unknown. Here, we demonstrated that β-catenin stabilization is a molecular signal subsequent to the onset of Tspan8 expression, and that, in turn, β-catenin triggers the direct transcriptional activation of Tspan8 expression, leading to melanoma invasion. Moreover, we showed that β-catenin activation systematically correlates with a high expression of Tspan8 protein in melanoma lesions from transgenic Nras; bcat* mice, as well as in deep penetrating naevi, a type of human pre-melanoma neoplasm characterized by a combined activation of β-catenin and MAP kinase signaling. Overall, our data suggest that β-catenin and Tspan8 are part of a positive feedback loop, which sustains a high Tspan8 expression level, conferring to melanoma cells the invasive properties required for tumor progression and dissemination.
由于其高度转移倾向,尽管最近开发了靶向和免疫治疗策略,黑色素瘤仍然是皮肤癌中最致命的形式。因此,了解黑色素瘤侵袭的分子机制仍然至关重要。我们之前已经对 Tspan8 进行了特征描述,因为它能够促使黑色素瘤细胞从其微环境中分离出来,并触发黑色素瘤细胞的侵袭性,但 Tspan8 调节侵袭过程的信号事件仍不清楚。在这里,我们证明β-catenin 的稳定是 Tspan8 表达开始后的一个分子信号,而β-catenin 反过来又触发 Tspan8 表达的直接转录激活,导致黑色素瘤侵袭。此外,我们还表明,β-catenin 的激活与转染 Nras; bcat* 小鼠的黑色素瘤病变中 Tspan8 蛋白的高表达以及深穿透痣(一种人类前黑色素瘤肿瘤,其特征是β-catenin 和 MAP 激酶信号的联合激活)中的 Tspan8 蛋白的高表达系统相关。总体而言,我们的数据表明β-catenin 和 Tspan8 是正反馈回路的一部分,该回路维持高水平的 Tspan8 表达,赋予黑色素瘤细胞肿瘤进展和扩散所需的侵袭特性。