实用肿瘤学杂志 ›› 2020, Vol. 34 ›› Issue (5): 398-403.doi: 10.11904/j.issn.1002-3070.2020.05.003

• 基础研究 • 上一篇    下一篇

LncRNA SOX2OT海绵吸附miR-34a促进SOX2表达增强大肠癌多药耐药

郭飘婷1, 邹阳2   

  1. 1.浙江中医药大学附属第二医院全科医学科(杭州 310005);
    2.浙江中医药大学附属第二医院骨科
  • 收稿日期:2020-04-04 出版日期:2020-10-28 发布日期:2020-11-02
  • 通讯作者: 郭飘婷,E-mail:522135842@qq.com
  • 作者简介:郭飘婷,女,(1990-),硕士,主治医师,从事中西医结合抗肿瘤相关的研究。
  • 基金资助:
    国家自然科学基金青年项目(编号:81803876)

LncRNA SOX2OT sponge adsorbs miR-34a to promote SOX2 expression and enhance multidrug resistance in colorectal cancer

GUO Piaoting1, ZOU Yang2   

  1. 1. Department of General Medicine,The Second Affiliated Hospital of Zhejiang University of Traditional Chinese Medicine,Hangzhou 310005,China;
    2. Department of Orthopedics,The Second Affiliated Hospital of Zhejiang University of Traditional Chinese Medicine
  • Received:2020-04-04 Online:2020-10-28 Published:2020-11-02

摘要: 目的 验证长链非编码RNA SOX2OT(Long noncoding RNA SOX2OT,SOX2OT)增强大肠癌HCT-116细胞多药耐药(Multidrug resistance,MDR),并从SOX2OT/miR-34a/SOX2信号通路探讨其可能的有效机制。方法 双荧光素酶报告基因验证SOX2OT与miR-34a、miR-34a与SOX2的靶向结合;HCT-116细胞瞬时转染SOX2OT质粒、miR-34a mimic,RT-qPCR验证转染效率;RT-qPCR检测SOX2OT、miR-34a和SOX2表达水平并进行相关性分析;CCK-8检测细胞增殖,评估SOX2OT、miR-34a对HCT-116细胞5-氟尿嘧啶(5-FU)、长春新碱(VCR)、顺铂(CDDP)、紫杉醇(TAXOL)化疗敏感性的影响。结果 SOX2OT与miR-34a、miR-34a与SOX2之间存在靶向关系;SOX2OT抑制miR-34a(P<0.05),上调SOX2(P<0.01);miR-34下调SOX2OT(P<0.01)和SOX2(P<0.01);转染SOX2OT质粒后HCT-116细胞的5-FU、VCR、CDDP、TAXOL的IC50值均升高(P<0.01);HCT-116细胞共转染SOX2OT、miR-34a mimic时对四种化疗药物的IC50值与转染SOX2OT组相比均明显降低(P<0.01),其中5-FU、CDDP的IC50值与对照组相比无统计学差异(P>0.05)。结论 SOX2OT海绵吸附miR-34a促进SOX2的表达致使HCT-116细胞多药耐药。

关键词: 大肠癌, 多药耐药, SOX2OT, miR-34a, SOX2

Abstract: Objective The aim of this study was to verify that long noncoding RNA SOX2OT(SOX2OT)enhanced the multidrug resistance(MDR)of colorectal cancer HCT-116 cells,and explored its possible effective mechanism on SOX2OT/miR-34a/SOX2 signaling pathway.Methods Dual luciferase reporter gene assay was used to verify the targeted binding of SOX2OT to miR-34a,and miR-34a to SOX2;The SOX2OT plasmid and miR-34a were transient transfected into HCT-116 cells,and the transfection efficiency was verified by RT-qPCR;RT-qPCR was used to detect the levels of SOX2OT,miR-34a and SOX2,and the correlation amongst them were analyzed;The CCK-8 assay was used to detect cell proliferation and to assess the influence of SOX2OT and miR-34a on the chemosensitivity of HCT-116 cells to 5-fluorouracil(5-FU),vincristine(VCR),cisplatin(CDDP),and paclitaxel(Taxol).Results There was a targeting relationship between SOX2OT and miR-34a,and miR-34a with SOX2;The SOX2OT inhibited miR-34a(P<0.05)and upregulated the level of SOX2(P<0.01);The MiR-34a down-regulated the expression of SOX2OT and SOX2(P<0.01);The IC50 values for 5-FU,VCR,CDDP,and TAXOL in HCT-116 cells were increased after transfection of SOX2OT plasmid(P<0.01);The IC50 values of four chemotherapy drugs in the co-transfected with SOX2OT and miR-34a mimic groups were significantly lower than those of the transfected SOX2OT group(P<0.01).The IC50 values of 5-FU and CDDP were not different from the control group(P>0.05).Conclusion The SOX2OT sponge adsorbs miR-34a and promotes the expression of SOX2,resulting in multidrug resistance of HCT-116 cells.

Key words: Colorectal cancer, Multidrug resistance, SOX2OT, miR-34a

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