口腔医学 ›› 2024, Vol. 44 ›› Issue (2): 88-93.doi: 10.13591/j.cnki.kqyx.2024.02.002

• 基础与临床研究 • 上一篇    下一篇

EP300对口腔鳞癌细胞增殖和迁移的影响

王亚培,罗玉春,刘为,刘畅,唐婉容()   

  1. 川北医学院附属医院口腔科,四川南充(637000)
  • 收稿日期:2023-07-06 出版日期:2024-02-28 发布日期:2024-02-04
  • 通讯作者: 唐婉容 E-mail:642533674@qq.com
  • 基金资助:
    南充市校合作课题(19SXHZ0350)

Effect of EP300 on the proliferation and migration of oral squamous carcinoma cells

WANG Yapei,LUO Yuchun,LIU Wei,LIU Chang,TANG Wanrong()   

  1. Department of Stomatology, Affiliated Hospital of North Sichuan Medical College, Nanchong 637000, China
  • Received:2023-07-06 Online:2024-02-28 Published:2024-02-04

摘要:

目的 探讨EP300在口腔鳞癌中的表达水平以及对口腔鳞癌细胞增殖、迁移的影响。方法 通过在线数据库收集并分析EP300基因在泛癌组织及正常组织中的表达差异。采用qRT-PCR和Western blot分别检测EP300在正常口腔黏膜上皮细胞株NOK和两种不同OSCC细胞株HSC3、UM1中的基因和蛋白表达水平;通过质粒转染沉默HSC3和UM1细胞株中EP300基因,平板克隆和CCK-8检测细胞增殖能力,划痕实验检测细胞迁移能力。结果 生信分析发现EP300在头颈部鳞癌HNSCC中的表达较癌旁组织显著上调;与NOK组比较,HSC3和UM1中EP300基因和蛋白表达水平显著增高(P<0.05),且HSC3和UM1两种细胞系的EP300内源性表达相对更高。CCK-8增殖实验和克隆形成实验检测发现,沉默EP300后HSC3和UM1的增殖能力明显降低(P<0.05);细胞划痕实验检测发现沉默EP300后HSC3和UM1的迁移能力明显降低(P<0.05)。结论 EP300在口腔鳞癌细胞株HSC3和UM1中高表达,EP300低表达能够抑制口腔鳞癌细胞的增殖和迁移。

关键词: EP300, 口腔鳞状细胞癌, 增殖, 迁移

Abstract:

Objective To investigate the expression level of EP300 in oral squamous carcinoma and its effect on the proliferation and migration of oral squamous carcinoma cells. Methods Differential expression of EP300 gene in pan-cancerous tissues and their normal tissues was collected and analysed through online database. The gene and protein expression levels of EP300 in the normal oral squamous epithelial cell line NOK and two different OSCC cell lines HSC3 and UM1 were detected by RT-PCR and Western blot, respectively; the EP300 gene was silenced in HSC3 and UM1 cell lines by plasmid transfection. Cell proliferation ability was detected by plate cloning and CCK-8, and cell migration ability was detected by scratch assay. Results Bioconductivity analysis revealed that EP300 expression was significantly upregulated in HNSC of head and neck tumors compared to paraneoplastic tissues. EP300 gene and protein expression levels were significantly higher in HSC3 and UM1 compared to the NOK group (P<0.05), and EP300 endogenous expression was relatively higher in both HSC3 and UM1 cell lines. CCK-8 proliferation assay and clone formation assay detected that the proliferation ability of HSC3 and UM1 was significantly reduced after EP300 silencing (P<0.05). Cell scratch assay detected that the migration ability of HSC3 and UM1 was significantly reduced after EP300 silencing (P<0.05). Conclusion EP300 was highly expressed in oral squamous carcinoma cell lines HSC3 and UM1, and low expression of EP300 inhibited the proliferation and migration of oral squamous carcinoma cells.

Key words: EP300, oral squamous cell carcinoma, proliferation, migration

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