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Updated: Apr 1, 2026

Development of Compendium for Esophageal Squamous Cell Carcinoma
Published on: April 12, 2024
Deregulation of miR-93 and miR-143 in human esophageal cancer
Mohammad Hossein Ansari1, Shiva Irani2, Houri Edalat1
1Research Center for Molecular Medicine, Medicine Faculty, Hamadan University of Medical Sciences, Hamadan, Iran.
Abstract:
Esophageal squamous cell carcinoma (ESCC) is the second and third most common malignancy in Iranian males and females, respectively. Treatment of ESCC is largely ineffective due to lack of detection at early stages of the disease. In recent years, miRNA, a small RNA molecule, has drawn much attention to researchers as a potential biomarker for esophageal cancer. miR-93 and miR-143 are two miRNA molecules reported to be frequently deregulated in various cancers, including prostate, stomach, cervix, and etc. The purpose of this study was to investigate the expression levels of these miRNAs and evaluate their diagnostic and therapeutic potential in esophageal squamous cell carcinoma. In this study, total RNA was extracted from 30 tumor tissues and 30 nontumor tissues of esophageal tumor margins, using RNX-plus solution. After validating the quality and quantity of total RNA, cDNAs of interest were synthesized using microRNA-specific cDNA Synthesis Kit. The expression level of miR-93 and miR-143 was evaluated using quantitative real-time PCR with miRNA-specific primers. Finally, the obtained data was analyzed by SPSS ver.20 software and paired t test was performed to observe the significance of difference between groups. The expression level of miR-93 was significantly increased and of miR-143 was significantly decreased in most of the examined tumor tissues, compared to nontumor tissues. Also, our findings did not detect correlation between mir-93 and mir-143 expressions in regard to stage and grade of the samples. These findings suggest that the deregulation of these miRNAs may play an important role in esophageal squamous cell carcinoma. Both miR-93 and miR-143 might be used as potential biomarkers in esophageal squamous cell carcinoma. However, more studies with large population of samples are necessary.
Insights
MicroRNA (miRNA) biomarkers miR-93 and miR-143 show altered expression in esophageal squamous cell carcinoma. Increased miR-93 and decreased miR-143 in tumors suggest their potential diagnostic role in early cancer detection.
Area of Science:
- Oncology
- Molecular Biology
- Biomarker Discovery
Background:
- Esophageal squamous cell carcinoma (ESCC) is a prevalent cancer with poor treatment outcomes due to late-stage diagnosis.
- MicroRNAs (miRNAs) are emerging as promising biomarkers for various cancers, including esophageal cancer.
- Specific miRNAs, such as miR-93 and miR-143, are known to be dysregulated in multiple tumor types.
Purpose of the Study:
- To investigate the expression levels of miR-93 and miR-143 in ESCC tissues.
- To evaluate the diagnostic and therapeutic potential of these miRNAs in ESCC.
- To explore the correlation between miRNA expression and clinicopathological features of ESCC.
Main Methods:
- Total RNA extraction from 30 ESCC tumor and 30 adjacent non-tumor tissues.
- cDNA synthesis using a microRNA-specific kit.
- Quantitative real-time PCR (qRT-PCR) with miRNA-specific primers to assess miR-93 and miR-143 expression.
- Statistical analysis using SPSS software with paired t-tests.
Main Results:
- miR-93 expression was significantly upregulated in most ESCC tumor tissues compared to non-tumor tissues.
- miR-143 expression was significantly downregulated in most ESCC tumor tissues compared to non-tumor tissues.
- No significant correlation was found between miR-93 and miR-143 expression levels and the stage or grade of ESCC.
Conclusions:
- Dysregulation of miR-93 and miR-143 plays a role in the pathogenesis of ESCC.
- These miRNAs hold potential as diagnostic biomarkers for esophageal squamous cell carcinoma.
- Further large-scale studies are warranted to validate their clinical utility.
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