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首页> 外文期刊>Medical Oncology >The quantitative analysis by stem-loop real-time PCR revealed the microRNA-34a, microRNA-155 and microRNA-200c overexpression in human colorectal cancer
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The quantitative analysis by stem-loop real-time PCR revealed the microRNA-34a, microRNA-155 and microRNA-200c overexpression in human colorectal cancer

机译:通过茎环实时PCR进行的定量分析揭示了人类大肠癌中的microRNA-34a,microRNA-155和microRNA-200c过表达

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摘要

The recently identified class of microRNAs (miRNAs) provided a new insight in cancer research. As the member of miRNAs family, miR-34a, miR-155 and miR-200c abnormalities have been found in various types of cancer. However, the relationship between these three miRNAs (miR-34a, miR-155 and miR-200c) and colorectal cancer is unclear. In this study, we applied stem-loop real-time PCR to quantitatively detect miR-34a, miR-155 and miR-200c expression in 109 pair-matched human colorectal cancers and the corresponding normal mucosa. MiR-34a (2.2-fold), miR-155 (2.3-fold) and miR-200c (3.1-fold) were all expressed at higher levels in colorectal cancer (P = 0.001, 0.005 and 0.001, respectively). In rectum, miR-34a and miR-200c were significantly upregulated (P = 0.006 and 0.007), while the miR-155 overexpression was not statistically significant (P = 0.083). In colon, the higher expression of three miRNAs was seen, however, without significant difference (P 0.05). We also found that the miR-34a expression was higher in rectal cancer having more advanced TNM stage (III + IV, P = 0.03). Then miR-200c expression was positively correlated with and sera CEA level of rectal cancer patients (P = 0.04). In conclusion, our results thus suggest that the overexpression of miR-34a, miR-155 and miR-200c be associated with the development of colorectal cancer, meanwhile miR-34a may be involved in the development and progression of rectal cancer. The more deeply and larger scale research are required to prove the correlation.
机译:最近确定的microRNA(miRNA)类为癌症研究提供了新的见识。作为miRNA家族的成员,已在各种类型的癌症中发现了miR-34a,miR-155和miR-200c异常。然而,这三种miRNA(miR-34a,miR-155和miR-200c)与结直肠癌之间的关系尚不清楚。在这项研究中,我们应用茎环实时PCR定量检测109对配对的人类大肠癌和相应正常黏膜中的miR-34a,miR-155和miR-200c表达。在大肠癌中,miR-34a(2.2倍),miR-155(2.3倍)和miR-200c(3.1倍)均以较高的水平表达(分别为P = 0.001、0.005和0.001)。在直肠中,miR-34a和miR-200c显着上调(P = 0.006和0.007),而miR-155的过表达没有统计学意义(P = 0.083)。在结肠中,观察到三种miRNA的较高表达,但无显着差异(P> 0.05)。我们还发现,miR-34a表达在TNM分期更高的直肠癌中更高(III + IV,P = 0.03)。然后,miR-200c表达与直肠癌患者的血清CEA水平呈正相关(P = 0.04)。总之,我们的结果因此表明,miR-34a,miR-155和miR-200c的过表达与结直肠癌的发展有关,而miR-34a可能与直肠癌的发展和进展有关。需要更深入和大规模的研究来证明相关性。

著录项

  • 来源
    《Medical Oncology》 |2012年第5期|p.3113-3118|共6页
  • 作者单位

    Department of Gastrointestinal Surgery, Institute of Digestive Surgery and National Key Laboratory of Biotherapy of West China Hospital, Sichuan University, Chengdu, Sichuan Province, China;

    Department of Gastrointestinal Surgery, Institute of Digestive Surgery and National Key Laboratory of Biotherapy of West China Hospital, Sichuan University, Chengdu, Sichuan Province, China;

    Department of Pediatric Surgery, West China Hospital, Sichuan University, Chengdu, Sichuan Province, China;

    Department of Gastrointestinal Surgery, Institute of Digestive Surgery and National Key Laboratory of Biotherapy of West China Hospital, Sichuan University, Chengdu, Sichuan Province, China;

    Department of Gastrointestinal Surgery, Institute of Digestive Surgery and National Key Laboratory of Biotherapy of West China Hospital, Sichuan University, Chengdu, Sichuan Province, China;

    Department of Gastrointestina;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    MicroRNA-34a; MicroRNA-155; MicroRNA-200c; Colorectal cancer; Stem-loop real-time RT-PCR;

    机译:MicroRNA-34a;MicroRNA-155;MicroRNA-200c;结直肠癌;茎环实时RT-PCR;

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