Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2019 Sep 16:2019:3717683.
doi: 10.1155/2019/3717683. eCollection 2019.

Altered Serum MicroRNA Profile May Serve as an Auxiliary Tool for Discriminating Aggressive Thyroid Carcinoma from Nonaggressive Thyroid Cancer and Benign Thyroid Nodules

Affiliations

Altered Serum MicroRNA Profile May Serve as an Auxiliary Tool for Discriminating Aggressive Thyroid Carcinoma from Nonaggressive Thyroid Cancer and Benign Thyroid Nodules

Aisen Zhang et al. Dis Markers. .

Abstract

Thyroid cancers are the most common malignancy of the endocrine system; however, there is no reliable blood biomarkers for thyroid cancer diagnosis and even for aggressive and nonaggressive thyroid cancers as well as benign nodule discrimination. The present study is aimed at evaluating whether circulating microRNA (miRNA) can differentiate aggressive and nonaggressive thyroid cancer from benign thyroid nodules. In this study, we performed a multiphase, case-control study to screen serum miRNA expression profile in 100 patients with papillary thyroid cancer (PTC), 15 patients with aggressive medullary thyroid carcinoma (MTC), 91 patients with benign nodules, and 89 healthy controls using TaqMan low-density array followed by extensive reverse transcription quantitative real-time PCR validation. The results showed that the serum levels of miR-222-3p, miR-17-5p, and miR-451a were markedly increased, while miR-146a-5p, miR-132-3p, and miR-183-3p were significantly decreased in the PTC and benign nodule groups compared with the control group. There was no difference in the miRNA expression profile between the PTC group and the benign nodule group. Nevertheless, the serum levels of miR-222-3p and miR-17-5p were significantly increased in the MTC group than the benign nodule and control group. Moreover, receiver operating characteristic curve analyses demonstrated that the 2 miRNAs and their panel can accurately discriminate MTC from the benign nodule group and healthy controls. These findings indicated that the altered circulating miRNAs may discriminate PTC and benign thyroid nodules from controls, and serum miR-222-3p and miR-17-5p have the potential to serve as auxiliary tools for diagnosing more aggressive thyroid carcinomas, such as MTC.

PubMed Disclaimer

Conflict of interest statement

The authors declare that there is no conflict of interest regarding the publication of this paper.

Figures

Figure 1
Figure 1
Overview of the design strategy.
Figure 2
Figure 2
The 6 serum miRNAs' signatures in the PTC group or the benign nodule group vs. the healthy control group. Relative expression levels of 6 miRNAs were measured in 100 PTC patients, 91 benign nodule patients, and 89 healthy control individuals with a TaqMan probe-based qRT-PCR assay. CT values were normalized to let-7d/g/i, and the relative expression was shown as 2-ΔCT. ∗∗P < 0.01, ∗∗∗P < 0.001.
Figure 3
Figure 3
The profile of 3 serum miRNAs in MTC. Relative expression levels of 3 miRNAs were measured in 15 MTC patients, 15 benign nodule patients, and 15 healthy control individuals with a TaqMan probe-based qRT-PCR assay. CT values were normalized to let-7d/g/i, and the relative expression was shown as 2-ΔCT. P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001.
Figure 4
Figure 4
The ROC curves of 2 serum miRNAs in the MTC patients compared with healthy controls or the benign nodule subjects. ROC curves indicate the ability of serum analysis of the 2 individual miRNAs, miR-222-3p and miR-17-5p, in individuals or combined, to differentiate cases of MTC from healthy controls (a–c) and the benign nodule subjects (d–f).

Similar articles

Cited by

References

    1. Pacini F., Castagna M. G. Approach to and treatment of differentiated thyroid carcinoma. Medical Clinics of North America. 2012;96(2):369–383. doi: 10.1016/j.mcna.2012.01.002. - DOI - PubMed
    1. Davies L., Welch H. G. Increasing incidence of thyroid cancer in the United States, 1973-2002. JAMA. 2006;295(18):2164–2167. doi: 10.1001/jama.295.18.2164. - DOI - PubMed
    1. Hegedus L. The thyroid nodule. The New England Journal of Medicine. 2004;351(17):1764–1771. doi: 10.1056/NEJMcp031436. - DOI - PubMed
    1. Mon S. Y., Hodak S. P. Molecular diagnostics for thyroid nodules: the current state of affairs. Endocrinology and Metabolism Clinics of North America. 2014;43(2):345–365. doi: 10.1016/j.ecl.2014.02.015. - DOI - PubMed
    1. Gharib H., Papini E., Paschke R., et al. American Association of Clinical Endocrinologists, Associazione Medici Endocrinologi, and European thyroid association medical guidelines for clinical practice for the diagnosis and management of thyroid nodules. Endocrine Practice. 2010;16(Supplement 1):1–43. doi: 10.4158/10024.GL. - DOI - PubMed

MeSH terms

Supplementary concepts