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miR-483与结直肠癌关系的研究 被引量:6

Correlation of miR-483 with Colorectal Cancer
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摘要 背景:胰岛素样生长因子2(IGF2)基因在多种恶性肿瘤中呈高表达,在肿瘤发生中起重要作用。miR-483位于IGF2基因第7号内含子中,与宿主基因共表达,但其具体功能尚未明确。目的:检测miR-483-3p、miR-483-5p在结直肠癌中的表达情况,探讨其作为结直肠癌分子标记物的可能性。方法:收集75对结直肠癌组织和相应癌旁非癌组织样本,以real-time PCR检测miR-483-3p、miR-483-5p表达并分析两者间以及两者与肿瘤临床病理特征的关系,以ROC曲线分析两者对结直肠癌的诊断性能。结果:结直肠癌组织中的miR-483-3p、miR-483-5p相对表达量均显著高于相应癌旁非癌组织(P<0.000 1),且两者在癌组织中的表达量呈显著正相关(rs=0.554 5,P<0.000 1)。miR-483-3p和miR-483-5p诊断结直肠癌的最佳截点分别为9.22和11.61,相应诊断敏感性、特异性分别为78.67%、62.67%和50.67%、85.33%;如两者联合检测(并联试验),诊断敏感性可提高至89.48%。两者表达与结直肠癌患者的性别、年龄以及肿瘤大小、部位、分化程度和TNM分期均无相关性。结论:miR-483-3p、miR-483-5p在结直肠癌中呈高表达,可能与肿瘤发生有关。两者有望成为结直肠癌诊断潜在的分子标记物。 Background:Insulin-like growth factor 2 (IGF2) is overexpressed in many human cancers and might play an important role in the onset of cancer.miR-483 is located within the seventh intron of IGF2 gene and is coexpressed with the host gene.However,the function of miR-483 remains unclear.Aims:To study the expressions of miR-483-3p and miR-483-5p in colorectal cancer (CRC) and their potential value as biomarkers of CRC.Methods:Cancerous and adjacent non-cancerous tissues from 75 CRC patients were collected.Expressions of miR-483-3p and miR-483-5p were determined by real-time PCR,and the correlations between miR-483-3p,miR-483-5p and clinicopathological characteristics of CRC were analyzed.The diagnostic performance of the two miRNAs for CRC was assessed by ROC curve.Results:Expression levels of miR-483-3p and miR-483-5p were significantly higher in cancerous tissue than in adjacent non-cancerous tissue (P 〈 0.000 1),and a significant positive correlation between the two miRNAs was seen in cancerous tissue (rs =0.554 5,P 〈 0.000 1).The cutoff value of miR-483-3p for CRC was 9.22 with a sensitivity of 78.67% and a specificity of 62.67%,while those of miR-483-5p are 11.61,50.67% and 85.33%,respectively.When these two miRNAs were combined in parallel,a sensitivity of 89.48% could be achieved.No obvious correlations were found between miR-483-3p,miR-483-5p expressions and the gender,age,tumor size,location,differentiation and TNM staging of CRC.Conclusions:miR-483-3p and miR-483-5p are highly expressed in CRC and might be involved in cancer onset.They might be used as potential biomarkers for diagnosis of CRC.
出处 《胃肠病学》 2014年第3期151-155,共5页 Chinese Journal of Gastroenterology
基金 国家自然科学基金面上项目资助(81171965 81372237)
关键词 结直肠肿瘤 miR-483 诊断 生物学标记 Colorectal Neoplasms miR-483 Diagnosis Biological Markers
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参考文献16

  • 1Bartel DP.MicroRNAs:genomics,biogenesis,mechanism,and function[J].Cell,2004,116 (2):281-297. 被引量:1
  • 2Zhang B,Pan X,Cobb GP,et al.microRNAs as oncogenes and tumor suppressors[J].Dev Biol,2007,302 (1):1-12. 被引量:1
  • 3Chen YW,Boyartchuk V,Lewis BC.Differential roles of insulin-like growth factor receptor-and insulin receptormediated signaling in the phenotypes of hepatocellular carcinoma cells[J].Neoplasia,2009,11 (9):835-845. 被引量:1
  • 4Zhao R,Berho M,Nogueras J,et al.Positive correlation of insulin-like growth factor-Ⅱ with proliferating cell index in patients with colorectal neoplasia[J].Cancer Epidemiol Biomarkers Prey,2005,14 (7):1819-1822. 被引量:1
  • 5Cui H.Loss of imprinting of IGF2 as an epigenetic marker for the risk of human cancer[J].Dis Markers,2007,23(1-2):105-112. 被引量:1
  • 6Jemal A,Bray F,Center MM,et al.Global cancer statistics[J].CA Cancer J Clin,2011,61 (2):69-90. 被引量:1
  • 7Miller S,Steele S.Novel molecular screening approaches in colorectal cancer[J].J Surg Oncol,2012,105 (5):459-467. 被引量:1
  • 8Ohdaira H,Sekiguchi M,Miyata K,et al.MicroRNA-494 suppresses cell proliferation and induces senescence in A549 lung cancer cells[J].Cell Prolif,2012,45 (1):32-38. 被引量:1
  • 9Gebeshuber CA,Martinez J.miR-1O0 suporesses IGF2 and inhibits breast tumorigenesis by interfering with proliferation and survival signaling[J].Oncogene,2013,32 (27):3306-3310. 被引量:1
  • 10Ge Y,Sun Y,Chen J.IGF-Ⅱ is regulated by microRNA-125b in skeletal myogenesis[J].J Cell Biol,2011,192 (1):69-81. 被引量:1

同被引文献79

  • 1徐希民,管纯梅,孙建丽,李朱福,诸月琴.血清维生素A和维生素C水平与大肠癌发病关系的探讨[J].实用肿瘤杂志,1989,4(3):153-155. 被引量:3
  • 2杨工,高玉堂,季步天,金凡,高汝聂,郑树.结、直肠癌与营养因素的流行病学研究[J].中华流行病学杂志,1994,15(5):299-303. 被引量:31
  • 3Muzny DM,Bainbridge MN,Chang K,et al.Comprehensive molecular characterization of human colon and rectal cancer[J].Nature,2012,487(7407):330-337. 被引量:1
  • 4Courtney RJ,Paul CL,Carey ML,et al.A population-based cross-sectional study of colorectal cancer screening practices of first-degree relatives of colorectal cancer patients[J].BMC Cancer,2013,13(1):1-11. 被引量:1
  • 5Dahan L,Norguet E,Etienne-Grimaldi MC,et al.Pharmacogenetic profiling and cetuximab outcome in patients with advanced colorectal cancer[J].BMC Cancer,2011,11(1):496. 被引量:1
  • 6Adelsten BA,Dobbins TA,Harris CA,et al.A systematic review and meta-analysis of KRAS status as determinant of response to anti-EGFR antibodies and impact of partner chemotherapy in metastatic colorectal cancer[J].Eur J Cancer,2011,47(9):1343-1354. 被引量:1
  • 7Lin AY,Buckley NS,Lu AT,et al.Effect of KRAS mutational status in advanced colorectal cancer on the outcomes of anti-epidermal growth factor receptor monoclonal antibody therapy:a systematic review and meta-analysis[J].Clin Colorectal Cancer,2011,10(1):63-69. 被引量:1
  • 8Greenwald P,Lanza E,Eddy GA,et al.Dietary fiber in the reduction of colon cancer risk[J].J Am Diet Assoc,1987,87(9):1178-1188. 被引量:1
  • 9Ghadirian P,Lacroix A,Maisonneuve P,et al.Nutritional factors and colon carcinoma:a case-control study involving French Canadians in Montreal,Quebec,Canada[J].Cancer,1997,80(5):858-864. 被引量:1
  • 10Hibler EA,Hu CC,Jurutka PW,et al.Polymorphic variation in the GC and CASR genes and associations with vitamin D metabolite concentration and metachronous colorectal neoplasia[J].Cancer,2012,21(2):368-375. 被引量:1

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