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DDX5和DDX17在卵巢癌组织中的表达及其临床意义 被引量:1

Expression of DDX5 and DDX17 in Ovarian Cancer Tissues and Their Clinical Significance
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摘要 目的:探究DDX5和DDX17在卵巢癌患者组织中的表达及临床意义。方法:采用实时荧光定量PCR检测卵巢癌组织、正常卵巢上皮细胞中DDX5和DDX17的相对表达量,进一步通过基因沉默技术,分别降低DDX5和DDX17的表达后,再采用CCK-8实验测定DDX5和DDX17对卵巢癌细胞增殖的影响。结果:卵巢癌组织中DDX5表达明显高于正常卵巢上皮细胞,而卵巢癌组织中DDX17表达明显低于正常卵巢上皮细胞(P<0.05);沉默DDX5表达后,卵巢癌细胞的增殖活性受到抑制。结论:DDX5和DDX17在卵巢癌组织异常表达,DDX5与卵巢癌细胞的增殖相关。 Objective:To investigate the expression and clinical significance of DDX5 and DDX17 in the tissues of patients with ovarian cancer.Methods:Real-time quantitative PCR was used to detect the relative expression of DDX5 and DDX17 in ovarian cancer tissue and normal ovarian epithelial cells.After further reducing the expression of DDX5 and DDX17 by gene silencing technology,the CCK-8 assay was used to determine the effects of ovarian cancer cell proliferation of DDX5 and DDX17.Results:The expression of DDX5 in ovarian cancer tissue was significantly higher than that in normal ovarian epithelial cells(P<0.05),and the expression of DDX17 in ovarian cancer tissue was significantly lower than that in normal ovarian epithelial cells(P<0.05).After silencing DDX5 expression,the proliferative activity of ovarian cancer cells was suppressed.Conclusion:DDX5 and DDX17 are abnormally expressed in ovarian cancer tissues,and DDX5 is related to the proliferation of ovarian cancer cells.
作者 朱国胜 邱丽影 资捷 ZHU Guosheng;QIU Liying;ZI Jie(Laboratory Department,Maternal and Child Health Hospital,Futian District,Shenzhen City,Guangdong Province 518045)
出处 《医学理论与实践》 2023年第10期1633-1635,1628,共4页 The Journal of Medical Theory and Practice
基金 深圳市福田区卫生公益性科研项目(FTWS2020038)。
关键词 DDX5 DDX17 卵巢癌 表达 DDX5 DDX17 Ovarian cancer Expression
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  • 1陈燕春,管英俊,刘焕彩,于丽,赵春艳.环磷酰胺对大鼠神经上皮细胞向神经元方向分化的影响[J].中国组织化学与细胞化学杂志,2009,18(1):71-76. 被引量:4
  • 2陈燕春,刘焕彩,周风华,赵春艳,杜红梅,丁昊宇,接琳琳.Beclin1和LC3Ⅱ在环磷酰胺致大鼠神经管畸形神经上皮细胞中的表达变化[J].解剖学杂志,2015,38(5):571-571. 被引量:2
  • 3Caretti G, Elissa PL. The DEAD box DdxS/Ddxl7 proteins and the noncoding RNA steroid receptor activator SRA. Cell Cycle,2007, 6 : 1172- 1176.
  • 4Jin W, Chen Y, Di GH,et al. Estrogen receptor (ER) β or p53 attenuates ERa-mediated transcriptional activation on the BRCA2 promoter. J Biol Chem, 2008, 283 : 29671 - 29680.
  • 5Wortham NC, Ahamed E, Nicol SM, et al. The DEAD-box protein p72 regulates ERa-/oestrogen-dependent transcrip- tion and cell growth, and is associated with improved surviv- al in ERa-positive breast cancer. Oncogene, 2009,28 : 4053 - 4064.
  • 6Mooney SM, Grande JP,Salisbury JL, et al. Sumoylation ofp68 and p72 RNA helicases affects protein stability and transactivation potential. Biochemistry ,2010, 49 : 1 - 10.
  • 7Chen GF, Guo XM, L FX,et al. Ddxl7 DEAD box RNA helicase is required for optimal function of the zinc-finger an- tiviral protein. Proc Natl Acad Sci USA, 2008,105 : 4352 - 4357.
  • 8Frances V, Fuller-Pace, All S. The DEAD box RNA heli- cases Ddx5 ( Ddx5 ) and Ddxl7 ( Ddxl7 ) : novel transcrip- tional co-regulators. Biochem Soc Trans, 2008,36 : 609-612.
  • 9Shin S, Rossow KL, Grande JP. Involvement of RNA heli- cases Ddx5 and Ddxl7 in colon cancer. Cancer Res,2007, 67 : 16 -31.
  • 10Shin S, Janknecht R. Concerted activation of the Mdm2 pro- moter by Ddxl7 RNA helicase and the coactivators p300 and P/CAF. J Cell Biochem, 2007,101 : 1252 - 1265.

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