基础医学与临床 ›› 2019, Vol. 39 ›› Issue (9): 1294-1299.

• 研究论文 • 上一篇    下一篇

HMG-CoA2裂解酶在鼻咽癌组织中表达及其对鼻咽癌细胞增殖、侵袭能力的影响

孙光炎1,丁明炎2,姚和迁2,曾凡杨2   

  1. 1. 湖北省汉川市人民医院
    2. 汉川市人民医院
  • 收稿日期:2018-10-19 修回日期:2018-12-24 出版日期:2019-09-05 发布日期:2019-09-06
  • 通讯作者: 丁明炎 E-mail:182196906@qq.com

Expression of HMG-CoA2-ligase in nasopharyngeal carcinoma and its influence on the cell proliferation and invasion of nasopharyngeal carcinoma cells

  • Received:2018-10-19 Revised:2018-12-24 Online:2019-09-05 Published:2019-09-06

摘要: 目的 探讨HMG-CoA2裂解酶(HMGCL)在鼻咽癌(NPC)组织中表达及其过表达对鼻咽癌细胞行为学的影响。方法 Western blot检测64例鼻咽癌组织和42例正常鼻咽上皮组织(NNE)及5个NPC细胞系(HK-1、CNE1、CNE2、HONE1和HNE-1)和正常鼻咽上皮细胞NP69中HMGCL表达水平;以HK-1细胞为研究对象,构建过表达HMGCL的细胞株;MTT法、集落形成实验、Transwell实验分别检测过表达HMGCL后HK-1细胞增殖、集落形成和迁移侵袭能力。结果 HMGCL在NPC和NPC细胞系中普遍低表达(P<0.05),在NNE和NP69细胞中普遍高表达(P<0.05);成功构建了过表达HMGCL的HK-1细胞株,过表达HMGCL后HK-1细胞增殖、集落形成和迁移侵袭能力均显著降低(P<0.05)。结论 HMGCL在鼻咽癌组织中低表达可能与鼻咽癌细胞恶性表型有关,为将来寻找抑制鼻咽癌发生进展提供了新的靶标。

关键词: 3-羟基-3-甲基戊糖-辅酶A 2裂解酶, 鼻咽癌, 增殖, 侵袭迁移

Abstract: Objective To investigate the expression of HMG-CoA2-ligase (HMGCL) in nasopharyngeal carcinoma (NPC) and its effect on the behavior of nasopharyngeal carcinoma cells. Methods The expression of HMGCL in 64 NPCs, 42 NNE tissues, 5 NPC cell lines (HK-1, CNE1, CNE2, HONE1, HNE-1) and normal nasopharyngeal epithelial cells NP69 were detected by Western blot. Taken HK-1 cells as the research object to construct overexpressing HMGCL cells. MTT assay, Colony formation assay and Transwell assay were used to detect the proliferation, colony formation, migration and invasion of HK-1 cells after HMGCL overexpression. Results HMGCL was highly expressed in NNE and NP69 cells, and lower in NPC and NPC cell lines. HK-1 cells overexpressing HMGCL were successfully constructed. The ability of cell proliferation, colony formation, migration and invasion were significantly reduced after overexpressing HMGCL. Conclusion The low expression of HMGCL in NPCs might be related to the malignant phenotype of NPC cells. This study provides a new target for inhibiting the progression of NPC in the future.

Key words: HMGCL, NPC, proliferation, metastasis