Signal transducer and activator of transcription-3 expression and activation is dysregulated in actinic cheilitis

J Cutan Pathol. 2007 Aug;34(8):606-11. doi: 10.1111/j.1600-0560.2006.00668.x.

Abstract

Background: The present study evaluates the signal transducer and activator of transcription-3 (STAT-3) expression and activation in actinic cheilitis (AC) and the relationship of this protein with the degree of epithelial dysplasia.

Methods: Twenty-five cases of AC were analyzed. Normal lip mucosa was used as a control group. AC lesions were graded as mild, moderate and severe dysplasias. Immunohistochemistry for STAT-3 and phospho-STAT-3 (STAT-3P) was performed using the biotin-streptavidin-peroxidase method, and the sections were evaluated by three blinded examiners.

Results: In normal lip mucosa, only cytoplasmic expression of STAT-3 was observed in the basal and parabasal layers. In AC, STAT-3 was expressed in the cell cytoplasm of the epithelial layers, except in the superficial layer. Nuclear expression of STAT-3 in occasional basal and parabasal cells was seen in moderate and severe dysplasias. In normal lip mucosa, nuclear expression of STAT-3P was found throughout the epithelium, except in the superficial layers, and it was more intense in the deeper layers. In AC, STAT-3P was also expressed in all layers, except for the superficial layer. However, in moderate and severe dysplasias, some epithelial cells exhibited loss of STAT-3P expression.

Conclusion: In AC, STAT-3 expression depends on the degree of dysplasia, and STAT-3 activation is dysregulated compared with normal tissue.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Biomarkers, Tumor / metabolism
  • Cheilitis / metabolism*
  • Cheilitis / pathology*
  • Epithelium / metabolism
  • Epithelium / pathology
  • Female
  • Humans
  • Immunoenzyme Techniques
  • Lip / metabolism
  • Lip / pathology
  • Male
  • Middle Aged
  • Photosensitivity Disorders / metabolism*
  • Photosensitivity Disorders / pathology*
  • Precancerous Conditions / metabolism
  • Precancerous Conditions / pathology
  • STAT3 Transcription Factor / metabolism*

Substances

  • Biomarkers, Tumor
  • STAT3 Transcription Factor
  • STAT3 protein, human