期刊文献+

靶向沉默人基因MDC1表达对食管癌细胞放射增敏作用的实验研究 被引量:4

Short hairpin RNA-mediated MDC1 gene silencing enhances the radiosensitivity of esophageal squamous cell carcinoma cell line ECA109
下载PDF
导出
摘要 目的利用RNA干扰技术抑制食管癌细胞ECA109细胞MDC1基因表达,观察其对细胞周期和放射敏感性的影响。方法构建MDC1基因的干扰质粒pMDC1-shRNA,与慢病毒包装质粒混合物共同转染293T细胞,收集病毒液,感染ECA109细胞,采用Real-TimePCR和westernblotting测定MDC1在mRNA水平和蛋白水平的表达。采用流式细胞术和克隆形成实验,检测RNA干扰对ECA109细胞放射敏感性的影响。结果成功构建pMDC1-shRNA质粒,转染ECA109细胞,获得稳定转染细胞株ECA109/MDC1,基因MDC1在mRNA水平和蛋白水平的表达均明显降低;5Gy射线照射后12h、24h、48h,ECA109/MDC1的G2/M期比例明显低于阴性对照组和空白对照组;ECA109、ECA109/NEGATIVE、ECA109/MDC1细胞的D0值分别为3.06Gy、2.90Gy、1.88Gy;SF2值分别为0.91、0.89、0.84;Dq值分别为1.59、1.47、1.20,显示ECA109/MDC1的D0值、SF2值、Dq值均明显降低。结论 RNAi技术可以有效地抑制食管癌细胞ECA109中基因MDC1的表达,从而增强ECA109细胞对放射线的敏感性。 Objective To explore the effect of MDC1 gene silencing by RNA interference on the radiosensitivity of human esophageal carcinoma cell line ECA109. Methods The vectors containing short hairpin RNA (shRNA) targeting MDC1 gene (pMDC1-shRNA) were cotransfected with pPACKH1-lentivector packaging system into 293T cells to package the lentivirus particles. Forty-eight hours after the transfection with specific or control lentiviral vectors, the stable integrants were selected using copGFP reporter gene; real-time RT-PCR and Western blotting were used to detect the expression levels of MDC1 mRNA and protein in the transfected ECA109 cells, respectively. The cell cycle distribution was measured with flow cytometry at 12, 24 and 48 h after a 5 Gy irradiation, and the radiosensitivity of esophageal carcinoma cell was evaluated by clone formation array. Results Sequence analysis confirmed correct insertion of MDC1-shRNA construct into pSIH1-H1-copGFP. The percentage of G2/M phase ECA109/ MDC1 cells was lower than that of ECA109 and ECA109/negative cells. The value of D0, SF2 and Dq of ECA109/ MDC1 cells were 1.88 Gy, 0.84 and 1.20, respectively, lower than those of ECA109 cells (3.06 Gy, 0.91 and 1.59) and those of ECA109/negative cells (2.90 Gy, 0.89 and 1.47). Conclusion RNA interference can inhibit MDC1 gene expression and enhance the radiosensitivity of ECA109 cells in vitro.
出处 《南方医科大学学报》 CAS CSCD 北大核心 2010年第8期1830-1834,共5页 Journal of Southern Medical University
基金 国家自然科学基金(30470524 30870743)
关键词 MDC1 细胞周期 放射敏感性 RNA干扰 MDC 1 cell cycle radiosensitivity RNA interference
  • 相关文献

参考文献15

  • 1DiTullio RAJr, Mochan TA, Venere M, et al. 53BPI functions in an ATM-dependent checkpoint pathway that is constitutively activated in human cancer [ J ]. Nat Cell Biol, 2002, 4(12): 998-1002.
  • 2Femandez-Capetillo O, Chen HT, Celeste I, et al. DNA damage- induced G(2)-M checkpoint activation by histone H2AX and 53BP 1 [J]. Nat Cell Biol, 2002, 4(12): 993-7.
  • 3Lou Z, Minter-Dykhouse K, Wu X, et al. MDCI is coupled to activated CHK2 in mammalian DNA damage response pathways [J]. Nature, 2003, 421(6926): 957-61.
  • 4Goldberg M, Stucki M, Falck J, et al. MDC1 is required for the intra-S-phase DNA damage checkpoint [J]. Nature, 2003, 421 (6926): 952-6.
  • 5Stewart GS, Wang B, Bignell CR, et al. MDCI is a mediator of the mammalian DNA damage checkpoint [ J ]. Nature, 2003, 421 (6926): 961-6.
  • 6Shang YL, Bodero AJ, Chen PL. NFBDI, a novel nuclear protein with signature motifs of FHA and BRCT, and an internal 41-amino acid repeat sequence, is an early participant in DNA damage response [ J ]. J Biol Chem, 2003, 278(8): 6323-9.
  • 7Lou Z, Chini CC, Minter-Dykhouse K, et al. Mediator of DNA damage checkpoint protein 1 regulates BRCAI localization and phosphorylation in DNA damage checkpoint control [J]. J Biol Chem, 2003, 278(16): 13599-602.
  • 8Peng A, Chen PL. NFBDI, like 53BP1. Is an early and redundant transducer mediating Chk2 phosphorylation in response to DNA damage[J]. J Biol Chem, 2003, 278(11): 8873-6.
  • 9Anbanandam A, Albarado DC, Tirziu DC, et al. Molecular basis for praline-and arginine-rich peptide inhibition of proteasome [ J ]. J Mol Biol, 2008, 384(1): 219-27.
  • 10Raju U, Nakata E, Yang P, et al. In vitro enhancement of tumor cell radiosensitivity by a selective inhibitor of cyclooxygenase-2 enzyme: mechanistic considerations [J]. Int J Radiat Oncol Biol Phys, 2002, 54(3): 886-94.

同被引文献20

引证文献4

二级引证文献7

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部