Engineering Research Center of Fujian University for Stomatological Biomaterials, Department of Stomatology and Affiliated Stomatological Hospital of Xiamen Medical College, Fujian, China.
Cancer Research Center, School of Medicine, Xiamen University, Xiamen, Fujian, China.
Cell Signal. 2019 Aug;60:81-90. doi: 10.1016/j.cellsig.2019.04.008. Epub 2019 Apr 15.
Integrin β6 (ITGB6), an epithelial-specific integrin, is upregulated in oral squamous cell carcinomas (OSCC) and is associated with progression and metastasis of OSCC. Lysophosphatidic acid (LPA), an important bioactive phospholipid present in saliva, has also been related to OSCC cell migration and invasiveness. LPA exerts its biological effects through signal transduction pathways that ultimately regulate gene expression. However, it is unclear whether LPA signaling is involved in ITGB6 upregulation in OSCC. Therefore, the aim of the current study was to investigate the role of LPA in the regulation of ITGB6 expression in OSCC cells, and to delineate the molecular signaling pathways involved. Using SAS and HSC-3 OSCC cell lines, we found that LPA increases ITGB6 mRNA expression without affecting mRNA stability, suggesting that LPA acts by regulating ITGB6 gene transcription. In addition, we show that LPA stimulation increases phosphorylation and binding of the transcription factors SMAD3 and ETS-1 to the ITGB6 promoter resulting in ITGB6 active transcription. Finally, we demonstrate that LPA-induced ITGB6 expression is mediated via the LPA receptors 1 (LPAR1) coupling to Gα. Our findings provide insights into the molecular mechanism underlying ITGB6 overexpression in OSCC and may have important implications for therapeutic purposes.
整合素β6(ITGB6)是一种上皮细胞特异性整合素,在口腔鳞状细胞癌(OSCC)中上调,与 OSCC 的进展和转移有关。溶血磷脂酸(LPA)是唾液中一种重要的生物活性磷脂,也与 OSCC 细胞迁移和侵袭有关。LPA 通过信号转导途径发挥其生物学效应,最终调节基因表达。然而,目前尚不清楚 LPA 信号是否参与 OSCC 中 ITGB6 的上调。因此,本研究旨在探讨 LPA 在 OSCC 细胞中调节 ITGB6 表达中的作用,并阐明涉及的分子信号通路。使用 SAS 和 HSC-3 OSCC 细胞系,我们发现 LPA 增加 ITGB6 mRNA 表达而不影响 mRNA 稳定性,表明 LPA 通过调节 ITGB6 基因转录起作用。此外,我们表明 LPA 刺激增加了转录因子 SMAD3 和 ETS-1 与 ITGB6 启动子的磷酸化和结合,导致 ITGB6 活性转录。最后,我们证明 LPA 诱导的 ITGB6 表达是通过 LPA 受体 1(LPAR1)与 Gα 的偶联介导的。我们的研究结果为 OSCC 中 ITGB6 过表达的分子机制提供了深入的了解,这可能对治疗目的具有重要意义。