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miR-21表达变化与结直肠癌肿瘤发生发展的关系 被引量:3

Relationship between expression of miR-21 and tumorigenesis and progression of colorectal cancer
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摘要 [目的]探讨结直肠癌组织中的微小RNA21(miR-21)表达与肿瘤发生发展的关系。[方法]选取我院2015年1月~2016年9月确诊的结直肠癌组织标本及其对应的癌旁组织标本各80例,采用实时荧光定量聚合酶链反应(qRT-PCR)技术检测2组的miR-21水平,并分析不同TNM分期、病理学分化程度、病理学类型、肿瘤直径、肿瘤位置、淋巴结转移结直肠癌组中的miR-21表达差异。[结果]结直肠癌组织中的miR-21表达强度显著高于癌旁组织,且差异有统计学意义(P<0.05);不同病理学类型、不同分化程度、不同病灶直径的结直肠癌组织中的miR-21表达强度组间比较,差异无统计学意义;在TNM分期(Ⅲ期+Ⅳ期)、发生淋巴结转移、不同预后结局的结肠癌组织中的miR-21表达强度显著地高于TNM分期(Ⅰ期+Ⅱ期)、未发生淋巴结转移的结直肠癌组织,差异有统计学意义(P<0.05)。结直肠癌患者TNM分期增高、发生淋巴结转移、miR-21表达上调是患者不良预后的独立危险因素(P<0.05)。[结论]结直肠癌组织中的miR-21表达强度显著上调,并且与肿瘤TNM分期增加、发生淋巴结转移及不良预后有关。 [Objective] To investigate the relationship between miR-21 expression and tumorigenesis in colorectal cancer tissues.[Methods]From January 2015 to September 2016,80 cases of colorectal cancer and 80 cases of paracancerous tissues were selected from our hospital.The miR-21 levels of the two groups were detected by real-time fluorescence quantitative polymerase chain reaction(qRT-PCR).The differences of miR-21 expression in colorectal cancer with different TNM stage,pathological differentiation,pathological type,tumor diameter,tumor location and lymph node metastasis were analyzed.[Results] The expression of miR-21 in colorectal cancer tissues was significantly higher than that in adjacent tissues,and the difference was statistically significant(P<0.05).There were no significant differences in the expression of miR-21 between colorectal cancer tissues with different pathological types,different degrees of differentiation,and different lesion diameters(P>0.05).The expression of miR-21 in colon cancer tissues with TNM stage(stage Ⅲ+Ⅳ),lymph node metastasis,and different prognosis outcomes was significantly higher than that of TNM stage(stage Ⅰ+Ⅱ)and colorectal without lymph node metastasis.The difference in cancer tissues was statistically significant(P<0.05).TNM staging,lymph node metastasis,and up-regulation of miR-21 expression in colorectal cancer patients were independent risk factors for poor prognosis(P<0.05).[Conclusion] The intensity of miR-21 expression in colorectal cancer tissues was significantly up-regulated,and was associated with increased tumor TNM stage,lymph node metastasis,and poor prognosis.
作者 周红霞 徐建光 贾洪春 王昊婧 ZHOU Hong-xia;XU Jian-guang;JIA Hong-chun;WANG Hao-jing(Digestive Endoscopy Center,Quzhou People's Hospital,Quzhou 324000,China)
出处 《中国中西医结合消化杂志》 CAS 2019年第12期939-942,共4页 Chinese Journal of Integrated Traditional and Western Medicine on Digestion
基金 国家卫生计生委医药卫生科技发展计划项目(No:W2015JZC20)
关键词 结肠癌 直肠癌 微小RNA21 实时荧光定量聚合酶链反应 Colon cancer rectal cancer microRNA21 qRT-PCR
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  • 1Flintoft L. Non-coding RNA: structure and function for In-cRNAs[J]. Nat Rev Genet, 2013, 14(9) :598.
  • 2He Y, Meng XM, Huang C, et al. Long noneoding RNAs: Novel insights into hepatocelluar carcinoma [ J ]. Cancer Lett, 2014, 344(1) :20-27.
  • 3Lu KH, Li W, Liu XH, et al. Long non-coding RNA MEG3 inhibits NSCLC cells proliferation and induces ap- optosis by affecting p53 expression [ J]. BMC Cancer, 2013, 13:461.
  • 4Qin R, Chen Z, Ding Y, et al. Long non-coding RNA MEG3 inhibits the proliferation of cervical carcinoma cells through the induction of cell cycle arrest and apoptosis [J]. Neoplasma, 2013, 60(5):486-492.
  • 5Sun M, Xia R, Jin F, et al. Downregnlated long nonco- ding RNA MEG3 is associated with poor prognosis and promotes cell proliferation in gastric cancer [ J ]. Tumour Biol, 2014, 35(2):1065-1073.
  • 6David P Bartel.MicroRNAs[J]. Cell . 2004 (2)
  • 7J.B. Kjersem,T. Ikdahl,O.C. Lingjaerde,T. Guren,K.M. Tveit,E.H. Kure.Plasma microRNAs predicting clinical outcome in metastatic colorectal cancer patients receiving first-line oxaliplatin-based treatment[J]. Molecular Oncology . 2014 (1)
  • 8Lim LP,Glasner ME, Yekta S, et al. Vertebrate microRNAgenes [ J ]. Science, 2003,299 ( 5612 ) : 1540.
  • 9Locke JM, Da Silva Xavier G, Dawe HR, et al. Increased expression of miR-187 in human islets from individuals with type 2 diabetes is associated with reduced glucose- stimulated insulin secretion [ J ]. Diabetologia, 2014, 57 (1) :122.
  • 10Kuster DW, Mulders J,Ten Cate FJ, et al. MicroRNA tran- scriptome profiling in cardiac tissue of hypertrophic cardio- myopathy patients with MYBPC3 mutations [ J l. J Mol Cell Cardio1,2013 ,65 :59.

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