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.

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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