医学分子生物学杂志 ›› 2025, Vol. 22 ›› Issue (1): 62-67.doi: 10.3870/j.issn.1672-8009.2025.01.010

• 论著 • 上一篇    下一篇

MYH11 激活 ERK / MAPK 信号通路诱导喉鳞状细胞癌细胞生长和转移 #br#

  

  1. 自贡市第一人民医院耳鼻咽喉头颈外科 四川省自贡市, 643000
  • 出版日期:2025-01-31 发布日期:2025-02-28
  • 基金资助:
    自贡市重点科技计划项目 (No. 2022ZCYKY07), 高质量发展重点研发科技计划项目 (No. 2024GZL04)

MYH11 Activates the ERK / MAPK Signaling Pathway and Induces Growth and Metastasis of Laryngeal Squamous Cell Carcinoma Cells #br#

  1. Department of Otolaryngology-Head and Neck Surgery, the First Peoples Hospital of Zigong City,Zigong, Sichuan, 643000, China
  • Online:2025-01-31 Published:2025-02-28

摘要: 目的 探究肌球蛋白重链 11 (myosin heavy chain 11, MYH11) 对喉鳞状细胞癌细胞恶性生物学行为的影响及机制方法 qRT-PCR 检测 MYH11 mRNA 在喉鳞状细胞癌组织以及喉鳞状细胞癌细胞中的表达喉鳞状细胞癌细胞 TU686 分为 si-MYH11 组和 si-NC 。 FD-LSC-1 细胞分为 MYH11 组和 Vector 。CCK8、 流式细胞术细胞划痕、 Transwell 实验分别用于检测细胞增殖凋亡迁移以及侵袭能力, 蛋白质印迹检测各组细胞 ERK 1 / 2 磷酸化水平及 MAPK 相对表达量结果 MYH11 高表达于喉鳞状细胞癌组织及细胞。 si-MYH11 TU686 细胞增殖迁移和侵袭能力显著低于 si-NC ( P< 0. 05), 细胞凋亡显著高于si-NC (P< 0. 01), ERK1 / 2 磷酸化水平及 MAPK 表达显著低于 si-NC (P< 0. 01)。 MYH11 TU686 细胞增殖迁移和侵袭能力显著高于 Vector ( P< 0. 05), 细胞凋亡显著低于 Vector ( P < 0. 01), ERK1 / 2 磷酸化水平及 MAPK 表达显著高于 Vector (P< 0. 01)。 结论 MYH11 激活 ERK / MAPK 信号通路而促进喉鳞状细胞癌细胞的增殖迁移和侵袭能力

关键词: MYH11, 喉鳞状细胞癌, 生长, 转移

Abstract: Objective To investigate the effect and mechanism of myosin heavy chain 11( MYH11 ) on the malignant biological behaviors of laryngeal squamous cell carcinomacells. Methods qRT-PCR was used to detect the expression level of MYH11 mRNA in laryngealsquamous cell carcinoma tissues and cells. Laryngeal squamous cell carcinoma cells TU686 were divided into 2 groups: si-MYH11 group and si-NC group. FD-LSC-1 cells were divided into 2 groups: MYH11 group and Vector group. CCK8, flow cytometry, wound-healing assay and Transwell assay were used to determine the cell proliferation, apoptosis, migration, and invasion abilities, respectively. Western blotting was used to detect the phosphorylation level of ERK1 / 2 and the expressionlevel of MAPK in each group of cells. Results MYH11 was highly expressed in laryngeal squamouscell carcinoma tissues and cells. The proliferation, migration, and invasion ability of TU686 cells inthe si-MYH11 group were significantly lower than those in the si-NC group ( P < 0. 05), and cell apoptosis was significantly higher than that in the si-NC group (P < 0. 01), the ERK1 / 2 phosphorylation level and MAPK expression level were significantly lower than those in the si-NC group (P< 0. 01). The proliferation, migration, and invasion ability of TU686 cells in the MYH11 groupwere significantly higher than those in the Vector group (P < 0. 05), and cell apoptosis was significantly lower than that in the Vector group ( P < 0. 01), the phosphorylation level of ERK1 / 2 and MAPK expression level were significantly higher than those in the Vector group (P < 0. 01). Conclusion MYH11 activates the ERK/ MAPK signaling pathway and promotes the proliferation, migration, and invasion of laryngeal squamous cell carcinoma cells.

Key words: MYH11, laryngeal squamous cell carcinoma, growth, migration

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