Expression of microRNAs 16, 20a, 150 and 155 in anal squamous intraepithelial lesions from high-risk groups

Andreia Albuquerque1,2, Mara Fernandes3, Oliver Stirrup4

  • 1Faculty of Medicine of the University of Porto, Porto, Portugal. a.albuquerque.dias@gmail.com.

Scientific Reports
|February 8, 2019
PubMed

Insights

microRNAs (miRNAs) were assessed in anal precancerous lesions. While no significant differences were found in miR-16, miR-20a, miR-150, and miR-155 expression, miR-155 showed an increasing trend in high-grade squamous intraepithelial lesions.

Area of Science:

  • Oncology
  • Molecular Biology
  • Genetics

Background:

  • Anal squamous intraepithelial lesions (ASIL), also known as anal intraepithelial neoplasia (AIN), are precancerous conditions.
  • MicroRNAs (miRNAs) are implicated in cervical carcinogenesis, but their role in anal precancerous lesions remains unassessed.

Purpose of the Study:

  • To evaluate the expression of specific miRNAs (miR-16, miR-20a, miR-150, miR-155) in various grades of ASIL.
  • To investigate potential correlations between miRNA expression and the progression of anal precancerous lesions.

Main Methods:

  • Biopsies from 105 patients undergoing anal cancer screening were analyzed.
  • Lesions were classified using the Lower Anogenital Squamous Terminology (LAST) and AIN classification.
  • Quantitative analysis of miR-16, miR-20a, miR-150, and miR-155 fold expression was performed.

Main Results:

  • No statistically significant differences in the fold expression of the studied miRNAs were observed between different grades of ASIL.
  • A non-significant increasing trend in miR-155 fold expression was noted from negative samples to high-grade squamous intraepithelial lesions (HSIL).
  • miR-155 showed the highest fold expression increase in both low-grade (LSIL) and HSIL compared to other miRNAs.

Conclusions:

  • The expression levels of miR-16, miR-20a, miR-150, and miR-155 do not significantly differ across grades of ASIL.
  • Further research may be warranted to explore the potential role of miR-155 in the progression of anal precancerous lesions, despite the current non-significant findings.

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