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一个 VEGF-A/SOX2/SRSF2 网络控制着肺癌细胞中 VEGFR1 前体 mRNA 的可变剪接。

A VEGF-A/SOX2/SRSF2 network controls VEGFR1 pre-mRNA alternative splicing in lung carcinoma cells.

机构信息

INSERM U1209, CNRS UMR5309, Institute For Advanced Biosciences, Grenoble, 38042, France.

Université Grenoble Alpes, Institut Albert Bonniot, Grenoble, 38041, France.

出版信息

Sci Rep. 2019 Jan 23;9(1):336. doi: 10.1038/s41598-018-36728-y.

Abstract

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.

摘要

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。

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