医学分子生物学杂志 ›› 2022, Vol. 19 ›› Issue (1): 26-32.doi: 10.3870/j.issn.1672-8009.2022.01.004

• 论著 • 上一篇    下一篇

沉默 lncRNA-H19 对甲状腺癌细胞增殖、 侵袭和细胞周期的影响 

  

  1. 厦门大学附属第一医院普外科 福建省厦门市, 361003 
  • 出版日期:2022-01-31 发布日期:2022-02-25
  • 基金资助:
    福建省自然科学基金(No. 2020J05208)

Effects of Silencing lncRNA-H19 on Proliferation, Invasion and Cell Cycle of Thyroid Cancer Cells 

  1. Department of General Surgery, The First Affiliated Hospital of Xiamen University, Xiamen, Fujian, 361003, China
  • Online:2022-01-31 Published:2022-02-25

摘要: 目的 探讨长链非编码 RNA (lncRNA) -H19 对甲状腺癌细胞增殖、 侵袭和细胞周期的影响。 方 法 检测 lncRNA-H19 在癌组织、 癌旁组织、 正常人甲状腺上皮细胞 TEC 及甲状腺癌细胞 KAT18、 FTC133、 BCPAP、 TPC-1 中的表达; 检测沉默 lncRNA-H19 对细胞增殖、 侵袭和细胞周期的影响。 结果 lncRNA-H19 在甲状腺癌组织和细胞系中高表达; 不同肿瘤大小、 N 分期、 TNM 分期患者的 lncRNA-H19 表达水平差异 显著 (P< 0. 05)。 沉默 lncRNA-H19 后, 48、 72 h 的细胞增殖率及克隆形成率、 穿膜细胞数、 微血管形成 数量均明显下降 (P< 0. 05); Ki67、 PCNA、 N-cadherin、 Fibronectin、 VEGF、 MMP-9、 MMP-14、 cyclin A、 CDK2、 CDK4、 cyclin D1 蛋白表达明显下调 (P< 0. 05), 而 E-cadherin 蛋白表达明显上调 (P< 0. 05)。 结 论 沉默 lncRNA-H19 可能通过调节周期相关蛋白表达调节 FTC133 细胞增殖、 侵袭及细胞周期。 

关键词: 甲状腺癌, 长链非编码 RNA, lncRNA-H19, 细胞增殖, 细胞侵袭, 细胞周期 

Abstract: Objective To explore the effects of long non-coding RNA (lncRNA) -H19 on the proliferation, invasion and cell cycle of thyroid cancer cells. Methods The expression of lncRNA-H19 in cancer tissues, para-cancerous tissues, normal human thyroid epithelial cells (TEC) and thyroid cancer cells (KAT18, FTC133, BCPAP, TPC-1) were detected. The effects of silencing lncRNA-H19 on cell proliferation, invasion and cell cycle were detected. Results The lncRNA-H19 was highly expressed in thyroid cancer tissues and cell lines. The expression levels of lncRNA-H19 among thyroid cancer patients with different tumor sizes, N staging and TNM staging were significantly different (P< 0. 05). After silencing lncRNA-H19, the cell proliferation rate, clone formation rate, number of migrating cells and number of microvessel formation at 48 h and 72 h were significantly decreased (P< 0. 05), the expression levels of Ki67, PCNA, N-cadherin, Fibronectin, VEGF, MMP-9, MMP-14, cyclin A, CDK2, CDK4 and cyclin D1 proteins were significantly decreased (P< 0. 05), and the expression level of E-cadherin protein was significantly increased (P< 0. 05). Conclusion Silencing lncRNA-H19 could regulate the proliferation, invasion and cell cycle of FTC133 by regulating the expression of cell cycle related proteins.

Key words: thyroid cancer, long non-coding RNA, lncRNA-H19, cell proliferation, cell invasion, cell cycle

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