留言板

尊敬的读者、作者、审稿人, 关于本刊的投稿、审稿、编辑和出版的任何问题, 您可以本页添加留言。我们将尽快给您答复。谢谢您的支持!

姓名
邮箱
手机号码
标题
留言内容
验证码
x

血清miR-31可用于非小细胞型肺癌诊断

刘日清 黄仁林 梁柱

刘日清, 黄仁林, 梁柱. 血清miR-31可用于非小细胞型肺癌诊断[J]. 分子影像学杂志, 2019, 42(3): 410-413. doi: 10.12122/j.issn.1674-4500.2019.03.30
引用本文: 刘日清, 黄仁林, 梁柱. 血清miR-31可用于非小细胞型肺癌诊断[J]. 分子影像学杂志, 2019, 42(3): 410-413. doi: 10.12122/j.issn.1674-4500.2019.03.30
Riqing LIU, Renlin HUANG, Zhu LIANG. Expression of serum miR-31 for the diagnosis of non-small cell lung cancer[J]. Journal of Molecular Imaging, 2019, 42(3): 410-413. doi: 10.12122/j.issn.1674-4500.2019.03.30
Citation: Riqing LIU, Renlin HUANG, Zhu LIANG. Expression of serum miR-31 for the diagnosis of non-small cell lung cancer[J]. Journal of Molecular Imaging, 2019, 42(3): 410-413. doi: 10.12122/j.issn.1674-4500.2019.03.30

血清miR-31可用于非小细胞型肺癌诊断

doi: 10.12122/j.issn.1674-4500.2019.03.30
基金项目: 广东省科技计划项目(20130319c)
详细信息
    作者简介:

    刘日清,副主任医师,E-mail:zjfylsj@126.com

    通讯作者:

    梁 柱,硕士,副主任医师,E-mail:zjfylsj@126.com

Expression of serum miR-31 for the diagnosis of non-small cell lung cancer

  • 摘要: 目的研究血清miR-31对非小细胞型肺癌的诊断价值。方法选取非小细胞型肺癌患者42名为研究对象,收集患者的肺癌组织、癌旁组织、血清,和正常人40例的血清,检测miR-31的表达水平。结果非小细胞型肺癌组织miR-31显著高于癌旁组织(P< 0.05),临床分期、是否存在淋巴结转移是影响miR-31表达水平的独立性危险因素(P< 0.05)。患者血清miRNA水平显著高于正常人血清(P< 0.05)。ROC曲线表明miRNA诊断非小细胞型肺癌的敏感性0.829,特异性0.763。结论miRNA可以作为非小细胞型细胞新的分子标志物。

     

  • 图  1  miR-31的PCR结果

    A:扩增曲线;B: 溶解曲线.

    图  2  组织miR-31和血清miR-31表达水平的相关性

    图  3  miR-31与NSCLC的ROC曲线

    表  1  NSCLC组织中miR-31表达与临床特征的单因素分析(Mean±SD

    参数 例数 miR-31表达量 t/F P
    年龄(岁) 0.802 0.427
     <45 19 5.99±9.07
     ≥45 23 5.35±3.92
    临床分期 −2.935 0.005
     I期 18 4.24±2454
     II期 14 5.38±3.19
     III期 10 6.89±2.67
    病理类型 1.087 0.355
     鳞癌 15 5.43±4.11
     腺癌 17 5.78±7.09
     大细胞癌 10 5.81±8.96
    病理分级 0.062 0.951
     低分化 22 5.67±6.63
     高分化 20 5.61±6.57
    淋巴结转移 −2.783 0.006
     无 24 4.76±7.41
     有 18 6.87±8.34
    下载: 导出CSV

    表  2  NSCLC组织中miR-31表达与临床特征的多因素分析

    参数 标准误 Wald df 95% CI P
    临床分期 0.579 5.553 1 0.335-3.238 0.019
    淋巴结转移 0.961 4.026 1 0.091-3.920 0.037
    下载: 导出CSV
  • [1] Chen X, Zhao J, Guan YH, et al. Prognostic value of 2-{[}F-18]fluoro-2-deoxy-D-glucose uptake as measured by PET scan in patients with non-small cell lung cancer[J]. Mol Med Rep, 2008, 1(6): 889-93.
    [2] Lin K, Xu T, He BS, et al. MicroRNA expression profiles predict progression and clinical outcome in lung adenocarcinoma[J]. Onco Targets Ther, 2016, 9(12): 5679-92.
    [3] Gallardo E, Navarro A, Vinolas N, et al. miR-34a as a prognostic marker of relapse in surgically resected non-small-cell lung cancer[J]. Carcinogenesis, 2009, 30(11): 1903-9. doi: 10.1093/carcin/bgp219
    [4] Zhao YF, He J, Yang L, et al. Histone deacetylase-3 modification of MicroRNA-31 promotes cell proliferation and aerobic glycolysis in breast cancer and is predictive of poor prognosis[J]. J Breast Cancer, 2018, 21(2): 112-23. doi: 10.4048/jbc.2018.21.2.112
    [5] Liu ZY, Bai J, Zhang LY, et al. Conditional knockout of microRNA-31 promotes the development of colitis associated cancer[J]. Biochem Biophys Res Commun, 2017, 490(1): 62-8. doi: 10.1016/j.bbrc.2017.06.012
    [6] Wang CJ, Zhou ZG, Wang L, et al. Clinicopathological significance of microRNA-31, -143 and -145 expression in colorectal cancer[J]. Dis Markers, 2009, 26(1): 27-34. doi: 10.1155/2009/921907
    [7] Li P, Wang QA, Wang HN. MicroRNA-204 inhibits the proliferation, migration and invasion of human lung cancer cells by targeting PCNA-1 and inhibits tumor growth in vivo[J]. Int J Mol Med, 2019, 43(3): 1149-56.
    [8] Ma Y, Li XE, Chen S, et al. MicroRNA-4458 suppresses migration and epithelial-mesenchymal transition via targeting HMGA1 in non-small-cell lung cancer cells[J]. Cancer Manag Res, 2019, 11(7): 637-49.
    [9] Amin NP, Mohindra P, Jabbour SK. Serum microRNA guiding personalized radiation therapy in non-small cell lung cancer[J]. J Thorac Dis, 2018, 10(33): S4108-12.
    [10] Hou S, Cheng Z, Wang W, et al. Ailanthone exerts an antitumor function on the development of human lung cancer by upregulating microRNA-195[J]. J Cell Biochem, 2018, 37(4): 380-93.
    [11] Li W, Jia MX, Deng J, et al. Down-regulation of microRNA-200b is a potential prognostic marker of lung cancer in southern-central Chinese population[J]. Saudi J Biol Sci, 2019, 26(1): 173-7. doi: 10.1016/j.sjbs.2018.08.023
    [12] Zhou Y, Zheng X, Chen LJ, et al. microRNA-181b suppresses the metastasis of lung cancer cells by targeting sex determining region y-related high mobility group-box 6(Sox6)[J]. Pathol Res Pract, 2019, 215(2): 335-42. doi: 10.1016/j.prp.2018.12.009
    [13] Stepicheva NA, Song JL. Function and regulation of MicroRNA-31 in development and disease[J]. Mol Reprod Dev, 2016, 83(8): 654-74. doi: 10.1002/mrd.22678
    [14] Yamagishi M, Nakano K, Miyake A, et al. Polycomb-Mediated loss of miR-31 activates NIK-Dependent NF-kappa B pathway in adult T cell leukemia and other cancers[J]. Cancer Cell, 2012, 21(1): 121-35. doi: 10.1016/j.ccr.2011.12.015
    [15] Vire E, Curtis C, Davalos V, et al. The breast cancer oncogene EMSY represses transcription of antimetastatic microRNA miR-31[J]. Mol Cell, 2014, 53(5): 806-18. doi: 10.1016/j.molcel.2014.01.029
    [16] Liu X, Sempere LF, Ouyang H, et al. MicroRNA-31 functions as an oncogenic microRNA in mouse and human lung cancer cells by repressing specific tumor suppressors[J]. J Clin Invest, 2010, 120(4): 1298-309. doi: 10.1172/JCI39566
    [17] Edmonds MD, Boyd KL, Moyo T, et al. MicroRNA-31 initiates lung tumorigenesis and promotes mutant KRAS-driven lung cancer[J]. J Clin Invest, 2016, 126(1): 349-64.
    [18] Vishnubalaji R, Hamam R, Abdulla MH, et al. Genome-wide mRNA and miRNA expression profiling reveal multiple regulatory networks in colorectal cancer[J]. Cell Death Dis, 2015, 6(10): e1614-26.
    [19] 王 昆, 胡早秀, 赵铁荣, 等. miRNA-31基因谱与宣威女性肺癌的相关性研究[J]. 云南医药, 2016, 28(1): 4-8.
    [20] 侯春英. MET-PI3K-Akt信号通路介导miRNA--31调控肺腺癌肿瘤干细胞功能[D]. 北京: 北京协和医学院, 2016.
  • 加载中
图(3) / 表(2)
计量
  • 文章访问数:  739
  • HTML全文浏览量:  362
  • PDF下载量:  8
  • 被引次数: 0
出版历程
  • 收稿日期:  2019-06-10
  • 刊出日期:  2019-07-01

目录

    /

    返回文章
    返回

    关于《分子影像学杂志》变更刊期通知

    各位专家、作者、读者:

    为了缩短出版时滞,促进科研成果的快速传播,我刊自2024年1月起,刊期由双月刊变更为月刊。本刊主要栏目有:基础研究、临床研究、技术方法、综述等。

    感谢各位专家、作者、读者长期以来对我刊的支持与厚爱!

    南方医科大学学报编辑部

    《分子影像学杂志》

    2023年12月27日