INSERM U1209, CNRS UMR5309, Institute For Advanced Biosciences, Grenoble, 38042, France.
Université Grenoble Alpes, Institut Albert Bonniot, Grenoble, 38041, France.
Sci Rep. 2019 Jan 23;9(1):336. doi: 10.1038/s41598-018-36728-y.
The splice variant sVEGFR1-i13 is a truncated version of the cell membrane-spanning VEGFR1 receptor that is devoid of its transmembrane and tyrosine kinase domains. We recently showed the contribution of sVEGFR1-i13 to the progression and the response of squamous lung carcinoma to anti-angiogenic therapies. In this study, we identify VEGF165, a splice variant of VEGF-A, as a regulator of sVEGFR1-i13 expression in these tumors, and further show that VEGF cooperates with the transcription factor SOX2 and the splicing factor SRSF2 to control sVEGFR1-i13 expression. We also demonstrate that anti-angiogenic therapies up-regulate sVEGFR1-i13 protein level in squamous lung carcinoma cells by a mechanism involving the VEGF/SOX2/SRSF2 network. Collectively, our results identify for the first time a signaling network that controls VEGFR1 pre-mRNA alternative splicing in cancer cells.
剪接变异体 sVEGFR1-i13 是跨膜 VEGFR1 受体的截断版本,缺乏跨膜和酪氨酸激酶结构域。我们最近表明 sVEGFR1-i13 对鳞状肺癌的进展和对抗血管生成治疗的反应有贡献。在这项研究中,我们确定了 VEGF165,即 VEGF-A 的剪接变体,是这些肿瘤中 sVEGFR1-i13 表达的调节剂,并进一步表明 VEGF 与转录因子 SOX2 和剪接因子 SRSF2 合作来控制 sVEGFR1-i13 的表达。我们还证明,抗血管生成治疗通过涉及 VEGF/SOX2/SRSF2 网络的机制上调鳞状肺癌细胞中 sVEGFR1-i13 蛋白水平。总之,我们的结果首次确定了一个信号网络,该网络控制癌细胞中 VEGFR1 前体 mRNA 的选择性剪接。