AI Article Synopsis

  • * Researchers analyzed 40 cases of various odontogenic lesions, using immunohistochemical methods to assess the expression of alpha-smooth muscle actin (α-SMA) in MFs.
  • * Findings showed that MFs were most prevalent in odontogenic keratocysts, with varying levels of α-SMA expression, indicating a complex distribution and arrangement that may impact the biological behavior of these lesions.

Article Abstract

Background: Odontogenic cysts and tumors exhibit different degrees of aggressiveness in their biological behavior. There has been evidence that the presence of myofibroblasts (MFs) at the invasion front promotes tumor invasion. Our study is based on the fact that MFs are important in the biological behavior of odontogenic cysts and tumors.

Aim: To assess immunohistochemically expression of alpha-smooth muscle actin (α-SMA) of MFs in odontogenic cysts and tumors and correlate this expression to their biological behavior.

Materials And Methods: The archival tissues collected for 1.5 years were obtained from the Department of Oral Pathology & Microbiology, People's Dental Academy, Bhopal (India). A total of 40 cases consisting of 10 cases each of odontogenic keratocysts, radicular cysts, dentigerous cysts and ameloblastomas formed the study group. An immunohistochemical analysis of α-SMA expression and localization was carried out.

Results: Mean MF counts were the highest in odontogenic keratocysts which was followed by ameloblastomas, entigerous cysts and radicular cysts. Weak α-SMA-expression was found in 50% of cases, moderate in 22.5% of cases, and intense - in 10% cases. MFs were arranged in the spindle, focal, or network patterns in 35; 27.5 and 20% of cases, respectively.

Conclusion: The analysis revealed that the MFs were distinctly heterogeneous in distribution and pattern of arrangement. This provided persuasive evidence that stroma of these lesions harbor MFs as reflected by α-SMA immunopositive cells.

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Source
http://dx.doi.org/10.32471/exp-oncology.2312-8852.vol-44-no-3.18676DOI Listing

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