School of Dentistry, College of Oral Medicine, Taipei Medical University, Taipei, Taiwan.
Division of Oral and Maxillofacial Surgery, Department of Dentistry, Wan Fang Hospital, Taipei Medical University, Taipei, Taiwan.
Environ Toxicol. 2018 May;33(5):545-554. doi: 10.1002/tox.22542. Epub 2018 Jan 31.
The metastasis of oral squamous cell carcinoma (OSCC) is one of the most important causes of cancer-related deaths. Thus, various therapeutic strategies have been developed to prevent the metastasis of OSCC. Salvianolic acid A (SAA), a traditional Chinese medicine, has antithrombosis, antiplatelet, anti-inflammation, and antitumor activities. Here, we provide molecular evidence indicating that SAA exerts its antimetastatic effects by markedly inhibiting the invasion and migration of oral squamous SCC-9 and SCC-25 cells. SCC-9 and SCC-25 cells were treated with various concentrations of SAA to further investigate the precise involvement of SAA in cancer metastasis. The results of zymography, and Western blotting indicated that SAA treatment may decrease matrix metallopoteinase-2 (MMP-2) expression. SAA also inhibited p-c-Raf, p-MEK1/2, and p-ERK1/2 protein expression. In addition, treating SCC-9 cells with U0126, a MEK-specific inhibitor, decreased MMP-2 expression and concomitantly inhibited cell migration. Our findings suggested that SAA inhibits the invasion and migration of OSCC by inhibiting the c-Raf/MEK/ERK pathways that control MMP-2 expression. Our findings provide new insights into the molecular mechanisms that underlie the antimetastatic effect of SAA and are thus valuable for the development of treatment strategies for metastatic OSCC.
口腔鳞状细胞癌(OSCC)的转移是癌症相关死亡的最重要原因之一。因此,已经开发了各种治疗策略来预防 OSCC 的转移。丹酚酸 A(SAA)是一种中药,具有抗血栓、抗血小板、抗炎和抗肿瘤作用。在这里,我们提供分子证据表明,SAA 通过显著抑制口腔鳞状 SCC-9 和 SCC-25 细胞的侵袭和迁移来发挥其抗转移作用。用不同浓度的 SAA 处理 SCC-9 和 SCC-25 细胞,以进一步研究 SAA 确切参与癌症转移的情况。明胶酶谱和 Western blot 分析表明,SAA 处理可能会降低基质金属蛋白酶-2(MMP-2)的表达。SAA 还抑制 p-c-Raf、p-MEK1/2 和 p-ERK1/2 蛋白的表达。此外,用 MEK 特异性抑制剂 U0126 处理 SCC-9 细胞可降低 MMP-2 的表达并同时抑制细胞迁移。我们的研究结果表明,SAA 通过抑制控制 MMP-2 表达的 c-Raf/MEK/ERK 途径来抑制 OSCC 的侵袭和迁移。我们的研究结果为 SAA 抗转移作用的分子机制提供了新的见解,因此对于开发治疗转移性 OSCC 的策略具有重要价值。