School and Hospital of Stomatology, Tianjin Medical University, Tianjin, China.
Hexi Women & Children Healthcare and Family Planning Service Center, Tianjin, China.
Med Oncol. 2022 Jul 19;39(10):154. doi: 10.1007/s12032-022-01746-4.
Oral squamous cell carcinoma (named OSCC) is considered the most frequent malignancy in oral cavity, which has become a rapid increasing problem for the global public health with unclear molecular mechanism. Previously, Tiam1 (T-lymphoma invasion and metastasis inducing factor 1) has been reported as a potential oncogene for OSCC. Here, we in-depth explored its signaling mechanism for the disorder. The mRNA and protein expression levels of primary differentially expressed genes (Tiam1, Fibulin-3, and MMP-7) were measured in different TNM stages of OSCC patients using RT-PCR and ELISA methods. Based on the analysis of human OSCC cell line CAL27, the relationships between these factors have been further investigated and the interactions were also examined. The luciferase reporter assay was established for the promoter region of MMP-7. Both the epithelial (E-cadherin) and mesenchymal protein markers (Vimentin and Snail) expressions were examined using western blotting. The mRNA and protein activities of Fibulin-3 declined as the increase of TNM stage. Inversely, the mRNA and protein levels of Tiam1 and MMP-7 elevated significantly as OSCC progressed. Tiam1 transfection in CAL27 cells stimulated the expression of MMP-7 by accelerating the nuclear translocation of β-catenin, which was opposite to the functions of Fibulin-3. Moreover, Tiam1 interacted directly with Fibulin-3. The Tiam1 induced OSCC epithelial-mesenchymal transition (EMT) via MMP-7 activation, which was dependent on the direct binding of β-catenin at the promoter region. Collectively, these results indicated that Tiam1 competed with Fibulin-3 for nuclear β-catenin translocation, which subsequently stimulated MMP-7 expression by TCF-4 domain interaction following EMT initiation in OSCC development. Our systematical work hypothesized an innovative signaling cassette for OSCC progression, which provided beneficial references for future clinical study.
口腔鳞状细胞癌(OSCC)被认为是口腔最常见的恶性肿瘤,其分子机制尚不清楚,但已成为全球公共卫生的一个迅速增长的问题。此前,Tiam1(T 淋巴细胞侵袭和转移诱导因子 1)已被报道为 OSCC 的潜在癌基因。在这里,我们深入探讨了其在疾病中的信号机制。使用 RT-PCR 和 ELISA 方法测量了不同 TNM 阶段 OSCC 患者中初级差异表达基因(Tiam1、Fibulin-3 和 MMP-7)的 mRNA 和蛋白表达水平。基于对人 OSCC 细胞系 CAL27 的分析,进一步研究了这些因素之间的关系,并检查了它们之间的相互作用。建立了 MMP-7 启动子区域的荧光素酶报告基因检测。使用 Western blot 检测上皮(E-钙粘蛋白)和间充质蛋白标志物(波形蛋白和 Snail)的表达。随着 TNM 阶段的增加,Fibulin-3 的 mRNA 和蛋白活性下降。相反,随着 OSCC 的进展,Tiam1 和 MMP-7 的 mRNA 和蛋白水平显著升高。CAL27 细胞中转染 Tiam1 通过加速β-连环蛋白的核易位刺激 MMP-7 的表达,这与 Fibulin-3 的功能相反。此外,Tiam1 与 Fibulin-3 直接相互作用。Tiam1 通过 MMP-7 激活诱导 OSCC 上皮-间充质转化(EMT),这依赖于β-连环蛋白在启动子区域的直接结合。总之,这些结果表明,Tiam1 与 Fibulin-3 竞争核β-连环蛋白易位,随后通过 TCF-4 结构域相互作用刺激 MMP-7 表达,从而启动 EMT,促进 OSCC 的发展。我们的系统工作假设了一个用于 OSCC 进展的创新信号级联,为未来的临床研究提供了有益的参考。