口腔医学 ›› 2025, Vol. 45 ›› Issue (7): 495-501.doi: 10.13591/j.cnki.kqyx.2025.07.003

• 基础与临床研究 • 上一篇    下一篇

miR-7975对口腔鳞状细胞癌恶性表型的影响

高腾1,2,3, 赵振远1,2,3, 赵梦然1,2,3, 刘婕1,2,3, 宋晓萌1,2,3()   

  1. 1 南京医科大学附属口腔医院口腔颌面外科,江苏南京(210029)
    2 口腔疾病研究与防治国家级重点实验室培育建设点,江苏南京(210029)
    3 江苏省口腔转化医学工程研究中心,江苏南京(210029)
  • 收稿日期:2025-02-03 出版日期:2025-07-28 发布日期:2025-07-24
  • 通讯作者: 宋晓萌 Tel:(025)85031881E-mail:Xiaomengsong@njmu.edu.cn
  • 基金资助:
    国家自然科学基金(81772887);江苏省科教能力提升工程——江苏省研究型医院(YJXYYJSDW4);江苏省医学创新中心(CXZX202227)

The effect of miR-7975 on the malignant phenotype of oral squamous cell carcinoma

GAO Teng1,2,3, ZHAO Zhenyuan1,2,3, ZHAO Mengran1,2,3, LIU Jie1,2,3, SONG Xiaomeng1,2,3()   

  1. Department of Oral and Maxillofacial Surgery, The Affiliated Stomatological Hospital of Nanjing Medical University, Nanjing 210029, China
  • Received:2025-02-03 Online:2025-07-28 Published:2025-07-24

摘要:

目的 探究miR-7975对口腔鳞状细胞癌(oral squamous cell carcinoma,OSCC)恶性表型的影响及可能机制。方法 本研究通过实时定量逆转录PCR实验(real-time quantitative reverse transcription PCR,qRT-PCR)比较了miR-7975在不同口腔细胞系中的表达水平。在OSCC细胞系HSC3及HN4中分别转染miR-7975 mimic以及miR-7975 inhibitor,利用集落形成实验、CCK8实验、Transwell实验及细胞划痕实验探究miR-7975对OSCC细胞恶性表型的影响。通过蛋白质免疫印迹实验(Western blot)研究上皮-间充质转化(epithelial-mesenchymal transition,EMT)及RAS/ERK信号通路相关蛋白表达水平的变化。通过裸鼠成瘤实验进一步验证miR-7975对体内成瘤的影响。结果 OSCC细胞中miR-7975表达下调。miR-7975过表达降低了OSCC细胞的增殖、迁移以及侵袭能力。相反,miR-7975表达下降则提高了OSCC细胞的增殖、迁移以及侵袭能力。过表达miR-7975后EMT相关蛋白E-cadherin表达上调,而N-cadherin、Vimentin、β-catenin、Snail和Slug则下降,RAS/ERK信号通路相关蛋白表达增多。miR-7975表达下降后EMT及RAS/ERK信号通路相关蛋白表达的变化相反。相比于对照组,过表达miR-7975后裸鼠皮下的成瘤体积及质量明显小于对照组,miR-7975表达下降后体内成瘤体积和质量明显增大。结论 miR-7975通过调控EMT及RAS/ERK信号通路,抑制OSCC的增殖、迁移和侵袭能力,从而发挥抑癌作用。

关键词: 口腔鳞状细胞癌, miR-7975, 上皮-间充质转化, RAS/ERK信号通路

Abstract:

Objective To investigate the effect of miR-7975 on the malignant phenotype of oral squamous cell carcinoma (OSCC) and its potential mechanisms. Methods This study compared the expression levels of miR-7975 in different oral cell lines by qRT-PCR. miR-7975 mimic and miR-7975 inhibitor were transfected into OSCC cell lines HSC3 and HN4 respectively. Colony formation assay, CCK8 assay, Transwell assay, and wound healing assay were conducted to evaluate the effects of miR-7975 on the malignant phenotype of OSCC cells. Western blot was employed to analyze changes in the expression of EMT related proteins and proteins associated with the RAS/ERK signaling pathway. Subcutaneous tumor model of nude mice was used to further validate the tumorigenic effect of miR-7975 in vivo. Results The expression of miR-7975 was downregulated in OSCC cells. Overexpression of miR-7975 reduced the proliferation, migration, and invasion abilities of OSCC cells, whereas downregulation of miR-7975 enhanced these abilities. After miR-7975 overexpression, the expression of the EMT-related protein E-cadherin was upregulated, while N-cadherin, Vimentin, β-catenin, Snail, and Slug were downregulated. Additionally, the expression of proteins related to the RAS/ERK signaling pathway increased. Conversely, the expression of EMT and RAS/ERK signaling pathway-related proteins showed opposite changes when miR-7975 was downregulated. Compared to the control group, the volume and weight of tumors formed in nude mice were significantly smaller after miR-7975 overexpression, while they were significantly larger when miR-7975 expression was reduced. Conclusion miR-7975 exerts its tumor-suppressive effects by inhibiting the proliferation, migration, and invasion of OSCC through the regulation of EMT and the RAS/ERK signaling pathway.

Key words: oral squamous cell carcinoma, miR-7975, epithelial-mesenchymal transition, RAS/ERK signaling pathway

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