Department of Oral Pathology, College of Dentistry, Gangneung-Wonju National University, 7 Jukheon-gil, Gangneung-si, Gangwon-do, Republic of Korea.
Department of Oral and Maxillofacial Surgery, College of Dentistry, Gangneung-Wonju National University, Gangneung, Republic of Korea.
BMC Oral Health. 2022 Sep 5;22(1):378. doi: 10.1186/s12903-022-02425-6.
Rapid metastasis of oral squamous cell carcinoma (OSCC) is associated with a poor prognosis and a high mortality rate. However, the molecular mechanisms underlying OSCC metastasis have not been fully elucidated. Although deregulated expression of microRNA (miRNA) has a crucial role in malignant cancer progression, the biological function of miRNA in OSCC progression remains unclear. This study aimed to investigate the function of miRNA-18a in OSCC metastatic regulation via hypoxia-inducible factor 1α (HIF-1α).
miRNA-18a-5p (miRNA-18a) expressions in patients with OSCC (n = 39) and in OSCC cell lines (e.g., YD-10B and HSC-2 cells) were analyzed using quantitative real-time polymerase chain reaction. HIF-1α protein expressions in OSCC cells treated with miRNA-18a mimics or combined with cobalt chloride were analyzed using western blotting. The miRNA-18a expression-dependent proliferation and invasion abilities of OSCC cells were analyzed using MTT assay, EdU assay, and a Transwell® insert system.
miRNA-18a expression was significantly lower in OSCC tissue than in the adjacent normal tissue. In OSCC cell lines, HIF-1α expression was significantly decreased by miRNA-18a mimic treatment. Furthermore, the migration and invasion abilities of OSCC cells were significantly decreased by miRNA-18a mimics and significantly increased by the overexpression of HIF-1α under hypoxic conditions relative to those abilities in cells treated only with miRNA-18a mimics.
miRNA-18a negatively affects HIF-1α expression and inhibits the metastasis of OSCC, thereby suggesting its potential as a therapeutic target for antimetastatic strategies in OSCC.
口腔鳞状细胞癌(OSCC)的快速转移与预后不良和高死亡率相关。然而,OSCC 转移的分子机制尚未完全阐明。尽管 microRNA(miRNA)的失调表达在恶性癌症进展中起着关键作用,但 miRNA 在 OSCC 进展中的生物学功能仍不清楚。本研究旨在通过缺氧诱导因子 1α(HIF-1α)研究 miRNA-18a 在 OSCC 转移调节中的功能。
采用定量实时聚合酶链反应分析 39 例 OSCC 患者和 OSCC 细胞系(如 YD-10B 和 HSC-2 细胞)中 miRNA-18a-5p(miRNA-18a)的表达。采用 Western blot 分析 OSCC 细胞在 miRNA-18a 模拟物处理或与钴氯化物联合处理后 HIF-1α 蛋白的表达。采用 MTT assay、EdU assay 和 Transwell®插入系统分析 miRNA-18a 表达依赖性 OSCC 细胞的增殖和侵袭能力。
OSCC 组织中 miRNA-18a 的表达明显低于相邻正常组织。在 OSCC 细胞系中,miRNA-18a 模拟物处理可显著降低 HIF-1α 的表达。此外,与仅用 miRNA-18a 模拟物处理的细胞相比,miRNA-18a 模拟物和缺氧条件下 HIF-1α 的过表达可显著降低 OSCC 细胞的迁移和侵袭能力。
miRNA-18a 负调控 HIF-1α 的表达,抑制 OSCC 的转移,提示其可能成为 OSCC 抗转移策略的治疗靶点。