实用肿瘤学杂志 ›› 2025, Vol. 39 ›› Issue (4): 306-315.doi: 10.11904/j.issn.1002-3070.2025.04.008

• 基础研究 • 上一篇    下一篇

LINC00511调节miR-150-5p/PHF1轴对结直肠癌细胞增殖、凋亡和上皮-间充质转化的影响

赵建刚, 刘义粉, 赵光远, 鲍双振, 刘防震, 尹长恒, 刘洪博   

  1. 衡水市人民医院胃肠外科(衡水 053000)
  • 收稿日期:2024-03-07 修回日期:2025-04-02 发布日期:2025-09-09
  • 通讯作者: 赵建刚,E-mail:275078746@qq.com
  • 作者简介:赵建刚,男,(1986—),主治医师,硕士,从事胃肠道恶性肿瘤相关的研究。
  • 基金资助:
    衡水市科技计划项目(编号:2020014045Z)

Impacts of LINC00511 on proliferation,apoptosis,and epithelial mesenchymal transition of colorectal cancer cells by regulating the miR-150-5p/PHF1 axis

ZHAO Jiangang, LIU Yifan, ZHAO Guangyuan, BAO Shuangzhen, LIU Fangzhen, YIN Changheng, LIU Hongbo   

  1. Department of Gastroenterology Surgery,Hengshui People's Hospital,Hengshui 053000,China
  • Received:2024-03-07 Revised:2025-04-02 Published:2025-09-09

摘要: 目的 探究LINC00511调节miR-150-5p/聚梳组蛋白家族指蛋白1(PHD family finger protein 1,PHF1)轴对结直肠癌细胞增殖、凋亡和上皮-间充质转化(epithelial-mesenchymal transformation,EMT)的影响。方法 收集2021年3月—2023年3月本院24例行手术治疗的结直肠癌患者的癌组织和癌旁组织;培养结直肠癌细胞株SW480并随机分为正常对照组(Ctrl组)、si-NC组、si-LINC00511组、si-LINC00511+inhibitor NC组、si-LINC00511+miR-150-5p inhibitor组。采用RT-qPCR法检测结直肠癌患者癌组织和癌旁组织以及SW480细胞的LINC00511、miR-150-5p和PHF1 mRNA表达水平;CCK-8法检测细胞增殖能力;Transwell实验检测细胞侵袭和迁移能力;流式细胞术检测细胞凋亡;免疫印迹法检测PHF1以及凋亡、EMT相关蛋白表达。双荧光素酶报告基因实验分别验证LINC00511与miR-150-5p、miR-150-5p和PHF1的关系。结果 与癌旁组织相比,结直肠癌患者癌组织中LINC00511、PHF1 mRNA表达增高,而miR-150-5p表达降低(P<0.001)。与si-NC组SW480细胞相比,si-LINC00511组SW480细胞的LINC00511表达、细胞增殖(OD450值)、细胞迁移和侵袭数目以及Bcl-2、PHF1、N-cadherin、vimentin蛋白表达水平显著降低(P<0.01),miR-150-5p表达水平、细胞凋亡率以及Bax和E-cadherin蛋白表达水平显著升高(P<0.001)。与si-LINC00511+inhibitor NC组SW480细胞相比,si-LINC00511+miR-150-5p inhibitor组的相应指标变化与上述相反(P<0.001)。LINC00511靶向负调控miR-150-5p表达,miR-150-5p靶向负调控PHF1表达。结论 敲低LINC00511可能通过促进miR-150-5p的表达,进而抑制PHF1的表达,对结直肠癌细胞增殖、EMT起到抑制作用,并诱导结直肠癌细胞凋亡。

关键词: LINC00511, miR-150-5p, 聚梳组蛋白家族指蛋白1, 结直肠癌, 上皮-间充质转化, 增殖, 凋亡

Abstract: Objective The aim of this study was to investigate the effects of LINC00511 on proliferation,apoptosis,and epithelial mesenchymal transition(EMT)of colorectal cancer cells regulating by the miR-150-5p/PHD family finger protein 1(PHF1)axis. Methods The tumor tissues and adjacent tissues were collected from 24 colorectal cancer patients who underwent surgical treatment in our hospital from March 2021 to March 2023.Colorectal cancer SW480 cells were cultured,and randomly separated into the normal control group(Ctrl group),si-NC group,si-LINC00511 group,si-LINC00511+inhibitor NC group,and si-LINC00511+miR-150-5p inhibitor group.RT-qPCR was used to detect the expression of LINC00511,miR-150-5p,and PHF1 mRNA in cancer tissues and adjacent tissues of colorectal cancer patients and SW480 cells.CCK-8 method was used to detect the proliferative ability in SW480 cells.Transwell experiment was used to detect cell invasion and migration abilities.Flow cytometry was applied to detect cell apoptosis.Immunoblotting was used to detect the expression of PHF1,apoptosis,and proteins related to EMT.The dual luciferase reporter gene experiment verified the relationship between LINC00511 and miR-150-5p,or between miR-150-5p and PHF1,respectively. Results Compared with adjacent tissues,the expression of LINC00511 and PHF1 mRNA increased in the tumor tissues of colorectal cancer patients,while the expression of miR-150-5p decreased(P<0.001).Compared with the si-NC group,the expression of LINC00511,cell proliferation(OD450 value),numbers of cell migration and invasion,and the expression of Bcl-2,PHF1,N-cadherin,and vimentin proteins in SW480 cells were significantly reduced in the si-LINC00511 group(P<0.01),while miR-150-5p,cell apoptosis rate,the expression of Bax and E-cadherin proteins were significantly increased(P<0.001).Compared with the si-LINC00511+inhibitor NC group,the changes in corresponding indicators of SW480 cells in the si-LINC00511+miR-150-5p inhibitor group were opposite to those mentioned above(P<0.001).LINC00511 had targeted negative regulation of miR-150-5p expression,while miR-150-5p targeted negative regulation of PHF1 expression. Conclusion Knockdown of LINC00511 may promote the expression of miR-150-5p,thereby inhibiting the expression of PHF1,suppressing colorectal cancer cell proliferation and EMT,and inducing apoptosis of colorectal cancer cells.

Key words: LINC00511, MiR-150-5p, PHD family finger protein 1, Colorectal cancer, Epithelial-mesenchymal transition, Proliferation, Apoptosis

中图分类号: