A two-microRNA signature predicts the progression of male thyroid cancer
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Updated: Oct 18, 2025

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
Bingyang Liu1, Haihong Shi1, Weigang Qiu1
1Department of Thyroid and Breast Surgery, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, Fujian 362000, People's Republic of China.
Abstract:
In various cancers, microRNAs (miRNAs) are abnormally expressed, including thyroid cancer (TC). In recent years, the incidence of TC has increased annually around the world. Compared with female patients, male TC patients are more likely to have a postoperative recurrence and lymph node metastasis, and hence need second treatments. However, the molecular biological processes underlying this phenomenon are not understood. Therefore, we collected data on miRNA expression and clinical information of male TC patients from The Cancer Genome Atlas (TCGA) database. Differentially expressed miRNAs were identified between male TC tissues and matched normal tissues. The Kaplan-Meier method, univariate and multivariate Cox regressions, and receiver operating characteristic curve analyses were performed to assess the association between miRNAs and the disease-free survival of male TC patients. Gene Ontology (GO) and the Kyoto Encyclopaedia of Gene and Genome (KEGG) enrichment analyses were then used to explore the function of miRNA target genes. Furthermore, we evaluated the ability of the miRNA biomarker to predict survival in female TC patients. As a result, a total of 118 differentially expressed miRNAs were identified, including 25 upregulated and 93 downregulated miRNAs. Among them, miR-451a and miR-16-1-3p were confirmed to be independent prognostic factors for the disease-free survival rate. The target genes of miR-451a and miR-16-1-3p were identified, and functional analysis showed that these genes were enriched in 25 Go and KEGG accessions, including cell signal transduction, motor adhesion, phagocytosis, regulation of transcription, cell proliferation, angiogenesis, etc. Neither miR-451a and miR-16-1-3p, nor a prediction model based on both miRNAs effectively predicted survival in female TC patients. In conclusion, both miR-451a and miR-16-1-3p may play important roles in the processes of male TC. The two-miRNA signature involving miR-1258 and miR-193a may serve as a novel prognostic biomarker for male TC patients.
Insights
MicroRNAs (miRNAs) like miR-451a and miR-16-1-3p are key in male thyroid cancer (TC) progression and survival. A signature of two miRNAs may predict outcomes in male TC patients.
Area of Science:
- Oncology
- Genetics
- Molecular Biology
Background:
- Thyroid cancer (TC) incidence is rising globally.
- Male TC patients exhibit higher recurrence and metastasis rates than females.
- Molecular mechanisms driving male TC disparities remain unclear.
Purpose of the Study:
- Investigate microRNA (miRNA) expression in male TC.
- Identify miRNA biomarkers for disease-free survival in male TC patients.
- Explore the functional roles of identified miRNAs in male TC.
Main Methods:
- Utilized The Cancer Genome Atlas (TCGA) database for male TC miRNA expression and clinical data.
- Identified differentially expressed miRNAs using statistical analyses.
- Performed survival analyses (Kaplan-Meier, Cox regression) and functional enrichment (GO, KEGG).
Main Results:
- Identified 118 differentially expressed miRNAs (25 upregulated, 93 downregulated).
- miR-451a and miR-16-1-3p emerged as independent prognostic factors for disease-free survival in males.
- Functional analysis linked their target genes to critical pathways like cell signaling and proliferation.
- The identified miRNAs did not predict survival in female TC patients.
Conclusions:
- miR-451a and miR-16-1-3p are implicated in male TC pathogenesis.
- A two-miRNA signature (miR-1258 and miR-193a) shows potential as a novel prognostic biomarker for male TC.
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