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. 2015:2015:435656.
doi: 10.1155/2015/435656. Epub 2015 May 3.

Circulating MicroRNA-21 Is a Potential Diagnostic Biomarker in Gastric Cancer

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Circulating MicroRNA-21 Is a Potential Diagnostic Biomarker in Gastric Cancer

Jianhong Wu et al. Dis Markers. 2015.

Abstract

MicroRNA-21 was upexpressed in gastric cancer (GC) indicating that it is a potential diagnostic biomarker for GC. In this study, 50 GC patients and 50 healthy controls were recruited. miR-21 levels in serum and peripheral blood mononuclear cells (PBMCs) were quantified using quantitative real-time PCR. CA199, and CEA were measured using electrochemiluminescence assay. The sensitivity and specificity of circulating miR-21, CA199 and CEA in GC diagnosis, the correlation of circulating miR-21 to clinicopathological features, and the diagnostic value of miR-21 in different GC stages were determined. The levels of miR-21 in both serum and PBMCs increased significantly in GC patients comparing to healthy controls; however, no correlation was observed between circulating miR-21 level and clinicopathological features. The sensitivity and specificity of miR-21 in serum and PBMCs, and CA199 and CEA in GC diagnosis were 88.4%, 79.6%, 81.3%, 73.4%, 60.5%, 55.9%, and 68.6%, 59.3%, respectively. The positive prediction rates of circulating miR-21 in GC stages I to IV were all around 90%, while those of CA199 and CEA were around or less than 50%. Our data suggest circulating miR-21 (both in serum and in PBMCs) can serve as a good biomarker for GC and could be used in diagnosis of early (stage I) and late GC (stage IV).

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Figures

Figure 1
Figure 1
qRT-PCR quantification of miR-21 in serum and PBMCs of GC patients and healthy controls. (a) Amplification curves of miR-21 and U6. (b) Melting curves of miR-21 and U6. (c) Ct values of U6 in serum and PBMCS from GC patients and healthy controls. (d) miR-21 levels in serum and PBMCs of GC patients and healthy controls. NS: not statistically significant; ∗∗∗ p < 0.001.
Figure 2
Figure 2
ROC analysis of CA199, CEA, and miR-21 in serum and PBMCs. An AUC value was given in each curve plot.

References

    1. Schanen B. C., Li X. Transcriptional regulation of mammalian miRNA genes. Genomics. 2011;97(1):1–6. doi: 10.1016/j.ygeno.2010.10.005. - DOI - PMC - PubMed
    1. Lagos-Quintana M., Rauhut R., Lendeckel W., Tuschl T. Identification of novel genes coding for small expressed RNAs. Science. 2001;294(5543):853–858. doi: 10.1126/science.1064921. - DOI - PubMed
    1. Sayed D., Abdellatif M. Micrornas in development and disease. Physiological Reviews. 2011;91(3):827–887. doi: 10.1152/physrev.00006.2010. - DOI - PubMed
    1. Krol J., Loedige I., Filipowicz W. The widespread regulation of microRNA biogenesis, function and decay. Nature Reviews Genetics. 2010;11(9):597–610. doi: 10.1038/nrg2843. - DOI - PubMed
    1. Shenouda S. K., Alahari S. K. MicroRNA function in cancer: oncogene or a tumor suppressor? Cancer and Metastasis Reviews. 2009;28(3-4):369–378. doi: 10.1007/s10555-009-9188-5. - DOI - PubMed

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