外科理论与实践 ›› 2025, Vol. 30 ›› Issue (04): 295-301.doi: 10.16139/j.1007-9610.2025.04.02

• 论著 • 上一篇    下一篇

miR-4674表达变化对BGC-823胃癌细胞系生物学特征的影响

袁小兵1, 朱建伟2()   

  1. 1.江苏省如皋市人民医院普通外科,江苏 如皋 226500
    2.南通大学附属医院胃肠外科,江苏 南通 226000
  • 收稿日期:2024-10-16 出版日期:2025-07-25 发布日期:2025-10-23
  • 通讯作者: 朱建伟,E-mail: jwzhumd@aliyun.com

Impact of miR-4674 expression changes on the biological characteristics of BGC-823 gastric cancer cell line

YUAN Xiaobing1, ZHU Jianwei2()   

  1. 1. Department of General Surgery, Rugao People's Hospital, Jiangsu Province, Jiangsu Rugao 226500, China
    2. Department of Gastrointestinal Surgery, Affiliated Hospital of Nantong University, Jiangsu Nantong 226000, China
  • Received:2024-10-16 Online:2025-07-25 Published:2025-10-23

摘要:

目的:以生物信息学研究为基础,探讨miR-4674表达变化对BGC-823胃癌细胞系生物学特征的影响。方法:通过生物信息学分析,得到与胃癌关系密切的研究靶点miR-4674,构建miR-4674模拟物(mimic)、抑制物(inhibitor)以及相关阴性对照(NC)转染至BGC-823细胞系。应用逆转录聚合酶链式反应(RT-PCR)方法检测BGC-823细胞中miR-4674的表达变化。应用噻唑蓝(MTT)法检测细胞增殖能力。应用Transwell培养体系检测细胞迁移能力,应用TUNEL检测细胞的凋亡情况。结果:与空白对照组以及转染NC的细胞比较,转染miR-4674 mimic的细胞中miR-4674表达水平明显升高,细胞的增殖与迁移能力均明显升高(P<0.05),而转染miR-4674 inhibitor的细胞中miR-4674表达水平明显降低,细胞的增殖与迁移能力均明显下降(P<0.05)。TUNEL检测结果显示,各组均未见到凋亡细胞。结论:在BGC-823胃癌细胞系抑制miR-4674表达降低其恶性程度,在BGC-823胃癌细胞系过表达miR-4674则促进其恶性程度,miR-4674可能是胃癌干预的治疗靶点,为胃癌的治疗提供了新的策略。

关键词: miR-4674, 胃癌, BGC-823细胞系, 恶性程度

Abstract:

Objective To explore the impact of miR-4674 expression changes on the biological characteristics of BGC-823 gastric cancer cell line based on bioinformatics research. Methods Through bioinformatics screening, miR-4674 was prioritized as a gastric cancer-associated miRNA. We constructed miR-4674 mimic, inhibitor, and corresponding negative control (NC) transfected into the BGC-823 cell line. Reverse transcription-polymerase chain reaction (RT-PCR) method was used to detect the expression changes of miR-4674 in BGC-823 cells. Functional assays included: MTT assay for cell proliferation ability; Transwell assay for migration capacity; TUNEL staining for cell apoptosis detection.Results Compared with the control group and cells transfected with NC, the level of miR-4674 was significantly increased in cells transfected with miR-4674 mimic, and the proliferation and migration abilities of the cells were significantly improved (P< 0.05). In cells transfected with miR-4674 inhibitor, the level of miR-4674 was significantly decreased, and the proliferation and migration abilities of the cells were significantly reduced (P<0.05). The result of TUNEL showed no significant differences in apoptotic rates were observed across all groups. Conclusions In the BGC-823 gastric cancer cell line, inhibition of miR-4674 expression can reduce its malignancy, while overexpression of miR-4674 can enhance its malignancy, suggesting its potential as a therapeutic target for gastric cancer intervention, providing a new strategy for the treatment of gastric cancer.

Key words: miR-4674, Gastric cancer, BGC-823 cell line, Malignancy degree

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