基础医学与临床 ›› 2025, Vol. 45 ›› Issue (5): 627-636.doi: 10.16352/j.issn.1001-6325.2025.05.0627

• 研究论文 • 上一篇    下一篇

LncRNA HIF1A-AS1通过干预HIF1A促进胃癌细胞系增殖

殷利军1, 卜阳1, 昂格勒玛2, 宋琳琳3*   

  1. 1.宁夏回族自治区人民医院 普通外科中心, 宁夏 银川 750000;
    2.宁夏医科大学 第一临床学院, 宁夏 银川 750000;
    3.宁夏医科大学总医院心脑血管病医院 妇科,宁夏 银川 750000
  • 收稿日期:2024-07-29 修回日期:2024-11-08 出版日期:2025-05-05 发布日期:2025-04-23
  • 通讯作者: * 42976260@qq.com
  • 基金资助:
    宁夏自然科学基金(2022AAC03376)

LncRNA HIF1A-AS1 promotes the proliferation of gastric cancer cell lines through interfering with HIF1A

YIN Lijun1, BO Yang1, Anggelema2, SONG Linlin3*   

  1. 1. Center of General Surgery, People′s Hospital of Ningxia Hui Autonomous Region, Yinchuan 750000;
    2. The First Clinical College of Ningxia Medical University, Yinchuan 750000;
    3. Department of Gynecology,Cardio-Cerebrovascular Disease Hospital, General Hospital of Ningxia Medical University, Yinchuan 750000, China
  • Received:2024-07-29 Revised:2024-11-08 Online:2025-05-05 Published:2025-04-23
  • Contact: * 42976260@qq.com

摘要: 目的 探索HIF1A-AS1对胃癌细胞系作用及其可能的作用机制。方法 生物信息学分析胃癌组织中HIF1A-AS1的表达情况;构建HIF1A-AS1的过表达和沉默BGC-823、MKN28细胞株,real-time PCR检测HIF1A-AS1的表达情况,CCK-8法完成细胞增殖检测,流式细胞测量术完成细胞凋亡检测,Western blot完成HIF1A蛋白在细胞质和细胞核中的表达检测,细胞免疫荧光完成HIF1A蛋白的入核检测。结果 成功构建了HIF1A-AS1过表达和沉默的BGC-823和MKN28细胞模型。CCK-8法结果显示,HIF1A-AS1的沉默使细胞增殖下降(P<0.05),HIF1A-AS1过表达则细胞增殖显著上升(P<0.05);细胞凋亡结果显示HIF1A-AS1的沉默使细胞凋亡显著上升(P<0.05),HIF1A-AS1-over组细胞凋亡显著降低(P<0.05);细胞免疫荧光显示结果显示HIF1A-AS1的沉默抑制HIF1A蛋白的入核现象,过表达则促进入核现象的发生;Western blot结果显示,HIF1A-AS1沉默使HIF1A细胞质蛋白的表达显著降低(P<0.05),HIF1A-AS1过表达则促使HIF1A细胞质蛋白的表达显著上升(P<0.05);HIF1A-AS1沉默促使HIF1A细胞核蛋白的表达显著降低(P<0.05),HIF1A-AS1过表达促使HIF1A细胞核蛋白的表达显著上升(P<0.05)。结论 HIF1A-AS1可能通过调控亲本基因HIF1A的表达促进胃癌细胞系BGC-823、MKN28的增殖,抑制凋亡。

关键词: 亲本基因控调, 入核, 增殖, 凋亡

Abstract: Objective To investigate the effects of HIF1A-AS1 on the proliferation and apoptosis of gastric cancer cells lines BGC-823 and MKN28 and its possible mechanism. Methods The expression of HIF1A-AS1 in gastric cancer tissues was analyzed by bioinformatics. HIF1A-AS1 over expression and silenced BGC-823 and MKN28 cell strains were constructed. HIF1A-AS1 expression was detected by real-time PCR, cell proliferation was detected by CCK-8 assay, and apoptosis was detected by flow cytometry. Western blot was used to detect the expression of HIF1A protein in cytoplasm and nucleus and cellular immunofluorescence was used to detect HIF1A protein into nucleus. Results Models of BGC-823 and MKN28 gastric cancer cells with HIF1A-AS1 over-expression and silence were successfully constructed.HIF1A-AS1 over-expression decreased cell proliferation (P<0.05), while HIF1A-AS1 over-expression significantly increased cell proliferation (P<0.05). HIF1A-AS1 silencing significantly increased the apoptosis (P<0.05), and HIF1A-AS1-over expression significantly decreased the apoptosis (P<0.05). HIF1A-AS1 silencing inhibited the nucleation of HIF1A protein and over-expression promoted the nucleation of HIF1A protein. HIF1A-AS1 silencing significantly decreased the expression of HIF1A cytoplasmic protein (P<0.05) and over-expression of HIF1A-AS1 significantly increased the expression of HIF1A cytoplasm protein (P<0.05). HIF1A-AS1 silencing significantly decreased the expression of HIF1A nuclear protein (P<0.05) while HIF1A-AS1 over-expression significantly increased the expression of HIF1A nuclear protein (P<0.05). Conclusions HIF1A-AS1 may promote the proliferation and inhibit apoptosis of BGC-823 and MKN28 gastric cancer cells by regulating the expression of parental gene HIF1A.

Key words: parental gene control, enter the nucleus, proliferation, apoptosis

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