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Published on: September 8, 2015
Prognostic significance of microRNA-100 in solid tumors: an updated meta-analysis
Jiangfeng Wang1, Miao Yu2, Shanghui Guan1
1Department of Radiation Oncology, Qilu Hospital of Shandong University, Jinan, People's Republic of China.
Objective:
The aim of this study was to identify prognostic significance of microRNA-100 (miR-100) in solid tumor.
Methods:
Literature search was conducted in databases such as PubMed, Embase, and Web of Science, using the following words "(microRNA-100 OR miR-100 OR mir100) AND (tumor OR neoplasm OR cancer OR carcinoma OR malignancy)." The search was updated up until July 10, 2016. Newcastle-Ottawa scale was used to evaluate the quality of studies. Pooled hazard ratio (HR) with 95% confidence interval (CI) for patients' survival was calculated by using a fixed-effects or a random-effects model on the basis of heterogeneity. Subgroup analysis, sensitive analysis, and meta-regression were used to investigate the sources of heterogeneity. Publication bias was evaluated by using Begg's and Egger's tests.
Results:
A total of 16 articles with 1,501 patients were included in the present meta-analysis. It was demonstrated that a lower expression of miR-100 plays a negative role in the overall survival (OS) of patients with solid tumor (HR =1.92; 95% CI =1.25-2.94). In addition, the association between miR-100 and prognosis was also revealed in the following subgroups: non-small-cell lung cancer (NSCLC; HR =2.46; 95% CI =1.98-3.06), epithelial ovarian cancer (EOC; HR =2.29, 95% CI =1.72-3.04), and bladder cancer (BC; HR =4.14, 95% CI =1.85-9.27).
Conclusion:
This meta-analysis indicates that lower expression of miR-100 is related to poorer OS in patients with solid tumor, especially in those with NSCLC, EOC, and BC. MiR-100 is a promising prognosis predictor and may be a potential target for therapy in the future.
Insights
Lower expression of microRNA-100 (miR-100) is linked to poorer overall survival in solid tumor patients. This finding is particularly significant in non-small-cell lung cancer, epithelial ovarian cancer, and bladder cancer cases.
Area of Science:
- Oncology
- Molecular Biology
- Biomarkers
Background:
- MicroRNAs (miRNAs) are small non-coding RNAs that regulate gene expression.
- Dysregulation of miRNAs is implicated in various cancers.
- microRNA-100 (miR-100) has emerged as a potential biomarker in cancer, but its prognostic significance in solid tumors requires comprehensive evaluation.
Purpose of the Study:
- To conduct a meta-analysis to determine the prognostic significance of microRNA-100 (miR-100) in patients with solid tumors.
- To investigate the association between miR-100 expression levels and overall survival (OS).
Main Methods:
- A systematic literature search was performed in PubMed, Embase, and Web of Science up to July 10, 2016.
- Included studies were assessed for quality using the Newcastle-Ottawa scale.
- Pooled hazard ratios (HR) with 95% confidence intervals (CI) were calculated using fixed- or random-effects models. Publication bias was assessed using Begg's and Egger's tests.
Main Results:
- A total of 16 studies comprising 1,501 patients were included in the meta-analysis.
- Lower expression of miR-100 was significantly associated with poorer OS in solid tumor patients (HR = 1.92; 95% CI = 1.25-2.94).
- Subgroup analyses revealed this association in non-small-cell lung cancer (NSCLC; HR = 2.46; 95% CI = 1.98-3.06), epithelial ovarian cancer (EOC; HR = 2.29; 95% CI = 1.72-3.04), and bladder cancer (BC; HR = 4.14; 95% CI = 1.85-9.27).
Conclusions:
- This meta-analysis concludes that reduced miR-100 expression is a significant predictor of poor OS in solid tumors, notably in NSCLC, EOC, and BC.
- miR-100 demonstrates potential as a prognostic biomarker.
- miR-100 may represent a future therapeutic target in cancer treatment.
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