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岭南现代临床外科 ›› 2017, Vol. 17 ›› Issue (06): 665-668.DOI: 10.3969/j.issn.1009-976X.2017.06.008

• 论著与临床研究 • 上一篇    下一篇

长链非编码RNA Lnc-DQ在肝癌组织中的表达及对其对SMMC7721细胞干性特征的影响

林泽伟 1 曾兵 2* 叶会霖 3 程帝 3 刘吉奎 1*   

  1. 1. 北京大学深圳医院肝胆外科 2. 广州医科大学附属第六医院 3. 中山大学孙逸仙纪念医院
  • 通讯作者: 刘吉奎
  • 基金资助:

    Lnc-DQ 通过 p300/CREB调控Treg细胞分化介导肝癌免疫逃逸的机制研究;SMYD3调控谷氨酰胺代谢促进肝内胆管癌进展的机制研究;SMYD3/SIRT3/GDH途径调控谷氨酰胺代谢促进肝内胆管癌进展的机制研究

Expression of Lnc-DQ in hepatocellular carcinoma and its role in regulating of the stemness characteristics of SMMC7721 cells

LIN Zewei1,ZENG Bing2,YE Huilin3,CHENG Di3,LIU Jikui1.   

  1. 1Hepatobiliary Surgery Department,Peking University Shenzhen Hospital,Guangdong 518036,China; 2Gastrointestinal Surgery Department,The Sixth Affiliated Hospital,Guangzhou Medical University,Guangdong 511518,China. 3Hepatopancreatobiliary Surgery Department, Sun Yat-sen Memorial Hospital,Sun Yat-sen University,Guangzhou 510120,China.
  • Online:2017-12-20 Published:2017-12-20
  • Contact: LIU Jikui

摘要: 目的 检测长链非编码RNALnc-DQ在肝癌组织中的表达,探讨其对肝癌SMMC7721细胞干性特征的影响。方法 采用实时定量反转录聚合酶链反应(RT-qPCR)检测Lnc-DQ在30例肝癌组织和癌旁组织中的表达;shRNA干扰下调Lnc-DQ在SMMC7721细胞中的表达,克隆形成和成球培养实验观察其对SMMC7721肿瘤干细胞特征的影响;流式细胞仪检测CD133+细胞亚群的比例。结果 Lnc-DQ在肝癌组织中的相对表达显著高于癌旁组织(3.24±0.34 vs 1.81±0.17),差异具有统计学意义(P<0.05)。shRNA转染可显著下调Lnc-DQ在SMMC7721细胞中的表达(P<0.05)。实验组细胞(sh-Lnc-DQ)克隆形成数为43.62±5.35,较对照组(sh-NC)显著减少(94.31±5.07),差异具有统计学意义(P<0.05)。成球培养实验显示sh-Lnc-DQ可显著抑制SMMC7721细胞的成球能力(P<0.05)。实验组细胞CD133+细胞比例显著低于对照组织(2.32%±0.25% vs 9.24%±0.69%),差异具有统计学意义(P<0.05)。结论 Lnc-DQ在肝癌中高表达,下调Lnc-DQ的表达能够抑制肝癌SMMC7721细胞的干性功能。

关键词: 长链非编码 RNA, Lnc-DQ, 肝癌, 干性特征

Abstract: Objective To investigate the expression of Lnc- DQ in hepatocellular carcinoma (HCC) and its role in regulating of the stemness characteristics of SMMC7721 cells. Methods The expression of Lnc- DQ was determined by real- time quantitative reverse transcriptase polymerase chain reaction(RT-qPCR)in HCC samples and cell lines. Cells were infected with negative control short hairpin RNAs(sh- NC)or specific shRNAs targeting Lnc- DQ (sh- Lnc- DQ)to generate stable Lnc- DQ knockdown cell lines. Colon formation ,anchorage- independent sphere formation and flow cytometry assays were used to analyze the effects of Lnc- DQ knockdown on the cancer stem- like phenotype of SMMC7721 cells. Results LncDQ was up-regulated in both HCC tissue samples and cell lines. shRNA transfection could significantly reduced the expression of Lnc-DQ in HCC cells. For colon formation assay,the colony number was 43.62±5.35 in sh-Lnc-DQ group,and was significantly lower than 94.31±5.07 in sh- NC group(P<0.05). The mammosphere number in sh- Lnc- DQ group was small and lower than in sh- NC group(P<0.05). The proportion of CD133 positive was 2.32% ± 0.25% in sh- Lnc- DQ group and 9.24% ± 0.69% in sh- NC group(P<0.05). Conclusion LncDQ was up- regulated in HCC and play an important role in the regulating of the stemness related characteristics of SMMC7721 cells.

Key words: long noncoding RNA Lnc-DQ, hepatocellular carcinoma, stemness characteristics

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