Department of Oral and Maxillofacial Surgery, - Plastic Surgery, University Medical Centre Mainz, Mainz, Germany.
Department of Otorhinolaryngology, University Medical Centre Mainz, Mainz, Germany.
J Oral Pathol Med. 2019 Oct;48(9):810-816. doi: 10.1111/jop.12893. Epub 2019 Jul 19.
The vascular endothelial growth factor (VEGF) is involved in tumorigenesis of the upper aerodigestive tract. Different single nucleotide polymorphisms (SNPs) turn the regulation of the VEGF gene into a highly complex process, particularly influenced by exogenic factors like cigarette smoke (CSE). Analysis of the SNP- and CSE-dependent VEGF-gene regulation can help to improve antiangiogenic therapies and prognosis. Therefore, the aim of this study was to analyse the influence of CSE on the SNP-dependent regulation of the VEGF-gene in vitro.
Human alveolar epithelial-like type-II cells (A549) were transfected with different SNPs and incubated with CSE. SNP- and CSE-dependent VEGF-promoter activity and mRNA stability was measured using qRT-PCR and Western blot analysis.
Transfection with SNP -460 (ATC) and incubation with 10% CSE resulted in +19% elevated VEGF-promoter activity (P < 0.05). Transfection with SNP -2578/-460 (CTC) and 10% CSE incubation resulted in a 14% reduction of VEGF-promoter activity (P < 0.05). Regarding mRNA stability, transfection with SNP +936 T allele led to half-life of 1.11 hours, which decreased to 0.2 hours after incubation with CSE. In contrast, on protein level SNP +936 T transfection showed a not significant increase up to 176% (P > 0.05), while incubation with CSE led to a significant decrease to 61% (P = 0.002).
Transcriptional regulation of the VEGF gene by SNP -460 (ATC) in combination with CSE represents a mechanism for elevated VEGF expression and may be associated with a worse prognosis. The influence of +SNP 936 on mRNA stability may be responsible for regulation of VEGF plasma levels.
血管内皮生长因子(VEGF)参与上呼吸道肿瘤的发生。不同的单核苷酸多态性(SNP)使 VEGF 基因的调控变得非常复杂,特别是受到外源性因素如香烟烟雾(CSE)的影响。分析 SNP 和 CSE 依赖性 VEGF 基因调控可以帮助改善抗血管生成治疗和预后。因此,本研究旨在分析 CSE 对体外 VEGF 基因 SNP 依赖性调节的影响。
用人肺泡上皮样 II 型细胞(A549)转染不同的 SNP,并与 CSE 孵育。使用 qRT-PCR 和 Western blot 分析检测 SNP 和 CSE 依赖性 VEGF 启动子活性和 mRNA 稳定性。
转染 SNP-460(ATC)并孵育 10% CSE 可使 VEGF 启动子活性升高 19%(P<0.05)。转染 SNP-2578/-460(CTC)并孵育 10% CSE 可使 VEGF 启动子活性降低 14%(P<0.05)。关于 mRNA 稳定性,转染 SNP+936 T 等位基因可使半衰期为 1.11 小时,孵育 CSE 后半衰期缩短至 0.2 小时。相比之下,SNP+936 T 转染在蛋白水平上显示出不显著的增加,增加至 176%(P>0.05),而孵育 CSE 后则显著降低至 61%(P=0.002)。
SNP-460(ATC)与 CSE 联合转录调控 VEGF 基因表达代表了一种升高 VEGF 表达的机制,可能与预后不良有关。+SNP936 对 mRNA 稳定性的影响可能负责调节 VEGF 血浆水平。