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MicroRNAs and their target mRNAs as potential biomarkers among smokers and non-smokers with lung adenocarcinoma

机译:MicroRNA和他们的目标MRNA是吸烟者和肺腺癌的非吸烟者中的潜在生物标志物

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摘要

Lung adenocarcinoma is one of the major causes of mortality. Current methods of diagnosis can be improved through identification of disease specific biomarkers. MicroRNAs are small non-coding regulators of gene expression, which can be potential biomarkers in various diseases. Thus, the main objective of this study was to gain mechanistic insights into genetic abnormalities occurring in lung adenocarcinoma by implementing an integrative analysis of miRNAs and mRNAs expression profiles in the case of both smokers and non-smokers. Differential expression was analysed by comparing publicly available lung adenocarcinoma samples with controls. Furthermore, weighted gene co-expression network analysis is performed which revealed mRNAs and miRNAs significantly correlated with lung adenocarcinoma. Moreover, an integrative analysis resulted in identification of several miRNA-mRNA pairs which were significantly dysregulated in non-smokers with lung adenocarcinoma. Also two pairs (miR-133b/Protein Kinase C Zeta (PRKCZ) and miR-557/STEAP3) were found specifically dysregulated in smokers. Pathway analysis further revealed their role in important signalling pathways including cell cycle. This analysis has not only increased the authors' understanding about lung adenocarcinoma but also proposed potential biomarkers. However, further wet laboratory studies are required for the validation of these potential biomarkers which can be used to diagnose lung adenocarcinoma.
机译:肺腺癌是死亡率的主要原因之一。通过鉴定疾病特异性生物标志物,可以提高目前的诊断方法。 MicroRNA是基因表达的小非编码调节剂,其可以是各种疾病的潜在生物标志物。因此,本研究的主要目的是通过在吸烟者和非吸烟者的情况下,通过实施MiRNA和MRNA表达型材的一致性分析来获得肺腺癌发生的机械洞察力。通过将公共可用的肺腺癌样品与对照进行比较来分析差异表达。此外,进行加权基因共表达网络分析,其显示与肺腺癌明显相关的MRNA和miRNA。此外,一致性分析导致鉴定几种miRNA-mRNA对,其在具有肺腺癌的非吸烟者中显着困扰。在吸烟者中,发现两对(miR-133b /蛋白激酶c zeta(prkcz)和mir-557 / steap3)。途径分析进一步揭示了它们在包括细胞周期的重要信号通路中的作用。这种分析不仅增加了作者对肺腺癌的理解,而且提出了潜在的生物标志物。然而,验证可用于诊断肺腺癌的潜在生物标志物所需的进一步潮湿实验室研究。

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  • 来源
    《IET systems biology》 |2019年第2期|69-76|共8页
  • 作者单位

    NUST RCMS Sect H-12 Islamabad Pakistan;

    NUST RCMS Sect H-12 Islamabad Pakistan;

    NUST RCMS Sect H-12 Islamabad Pakistan;

    NUST RCMS Sect H-12 Islamabad Pakistan;

    NUST RCMS Sect H-12 Islamabad Pakistan;

    NUST RCMS Sect H-12 Islamabad Pakistan;

    Manchester Metropolitan Univ Sch Comp Math & Digital Technol GM459 Geoffrey Manton Bldg Manchester Lancs England;

    NUST Atta Ur Rahman Sch Appl Biosci ASAB Sect H-12 Islamabad Pakistan;

    NUST RCMS Sect H-12 Islamabad Pakistan;

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  • 正文语种 eng
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