Proliferation, apoptosis, and survivin expression in a spectrum of melanocytic nevi

Scott R Florell1, Anneli R Bowen, Adrianne N Hanks

  • 1Department of Dermatology, University of Utah, Salt Lake City, UT 84112, USA.

Abstract

Insights

Survivin is consistently found in benign melanocytic nevi, with rare apoptotic cells observed. This suggests a dysregulation of apoptosis, leading to cell accumulation in these skin neoplasms.

Area of Science:

  • Dermatopathology
  • Molecular Biology
  • Oncology

Background:

  • Apoptosis is crucial for tissue balance and is often altered in skin cancers.
  • Survivin, an apoptosis inhibitor, is present in various skin tumors but its role in melanocytic nevi was unstudied.
  • Melanocytic nevi are common benign skin growths of melanocyte origin.

Purpose of the Study:

  • To investigate the expression pattern of survivin in different types of benign melanocytic nevi.
  • To compare survivin expression with markers of cell proliferation and apoptosis in these nevi.
  • To understand the role of survivin in the pathogenesis of benign melanocytic lesions.

Main Methods:

  • In situ hybridization was used to detect survivin expression in six types of melanocytic nevi.
  • Apoptotic index was assessed using terminal deoxynucleotidyl transferase (TdT)-mediated dUTP nick end labeling (TUNEL).
  • Proliferating cell nuclear antigen (PCNA) immunostaining was employed to determine the proliferation index.

Main Results:

  • Survivin was expressed in all evaluated benign melanocytic nevi, including compound dysplastic, intradermal, compound, neurotized intradermal, and Spitz nevi.
  • The apoptotic rate was low across most nevi types, with no apoptotic cells detected in neurotized nevi.
  • Spitz nevi exhibited the highest proliferation index, while other nevi showed minimal proliferation.

Conclusions:

  • Consistent survivin expression in benign melanocytic lesions suggests its involvement in their development.
  • The rare identification of apoptotic cells points to a potential dysregulation of apoptotic pathways.
  • These findings imply that impaired apoptosis contributes to cell accumulation in benign melanocytic neoplasms.

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