Department of Oral and Maxillofacial Surgery, Key Laboratory of Oral Diseases of Traditional Chinese Medicine, Jiangxi University of Chinese Medicine, Nanchang, Jiangxi Province, China, 330006.
Department of Oral and Maxillofacial Surgery, Key Laboratory of Oral Diseases of Traditional Chinese Medicine, Jiangxi University of Chinese Medicine, Nanchang, Jiangxi Province, China, 330006; School of Stomatology, Nanchang University, Nanchang, Jiangxi Province, China, 330036.
J Stomatol Oral Maxillofac Surg. 2023 Dec;124(6S):101611. doi: 10.1016/j.jormas.2023.101611. Epub 2023 Aug 22.
Tongue squamous cell carcinoma (TSCC) is one of the most common malignant tumors of head and neck. Its incidence is on the rise, and the proportion of young patients is gradually increasing, which is prone to tumor recurrence and metastasis. At present, there is no effective method to completely treat TSCC. Studies have shown that brucea javanica oil (BJO) has good antitumor activity against lung cancer and gastrointestinal tumors, but its therapeutic effect on TSCC is not clear. We have previously confirmed that oleic acid, the main component of BJO, can induce apoptosis of TSCC and reduce its invasion and metastasis ability. However, the anticancer effect and mechanism of BJO in TSCC remain unclear. In order to further explore the effects of BJO on the biological characteristics of TSCC cells, we studied the effects of different concentrations of BJO on the migration, invasion ability and epithelial mesenchymal transition (EMT) progression of TSCC cells and the possible mechanisms through in vitro experiments. We found that BJO could inhibit the invasion and metastasis of TSCC and up-regulate miR-138. After BJO treatment, the expression of E-cad was significantly increased, while the expression of EZH2, Slug, p-ERK1/2 and Vimentin was significantly decreased. EZH2 is a miR-138 target gene involved in TSCC. BJO inhibits TSCC invasion and metastasis by regulating the miR-138-EZH2 pathway. In vivo experiments have also well demonstrated the targeting effect of this pathway. This study provides a new therapeutic strategy for the treatment of TSCC.
舌鳞状细胞癌(TSCC)是头颈部最常见的恶性肿瘤之一。其发病率呈上升趋势,且青年患者比例逐渐增加,易发生肿瘤复发和转移。目前,尚无有效方法可完全治疗 TSCC。研究表明,鸦胆子油(BJO)对肺癌和胃肠道肿瘤具有良好的抗肿瘤活性,但对 TSCC 的治疗效果尚不清楚。我们之前已经证实,BJO 的主要成分油酸可以诱导 TSCC 细胞凋亡,降低其侵袭和转移能力。然而,BJO 治疗 TSCC 的抗癌作用和机制仍不清楚。为了进一步探讨 BJO 对 TSCC 细胞生物学特性的影响,我们通过体外实验研究了不同浓度的 BJO 对 TSCC 细胞迁移、侵袭能力和上皮间质转化(EMT)进展的影响及其可能的机制。我们发现 BJO 可以抑制 TSCC 的侵袭和转移,并上调 miR-138。BJO 处理后,E-cad 的表达明显增加,而 EZH2、Slug、p-ERK1/2 和 Vimentin 的表达明显降低。EZH2 是参与 TSCC 的 miR-138 靶基因。BJO 通过调节 miR-138-EZH2 通路抑制 TSCC 的侵袭和转移。体内实验也很好地证明了该通路的靶向作用。本研究为 TSCC 的治疗提供了新的治疗策略。