Expression of programmed cell death protein 4 (PDCD4) and miR-21 in urothelial carcinoma

Biochem Biophys Res Commun. 2012 Jan 6;417(1):29-34. doi: 10.1016/j.bbrc.2011.11.035. Epub 2011 Nov 19.

Abstract

Background: We investigated the role of the programmed cell death 4 (PDCD4) tumor suppressor gene in specimens of transitional cell carcinoma and of healthy individuals.

Methods: PDCD4 immunohistochemical expression was investigated in 294 cases in histologically proven transitional cell carcinoma in different tumorous stages (28 controls, 122 non-muscle invasive urothelial carcinoma, stages Tis-T1, 119 invasive transitional cell carcinoma stages T2-T4 and 25 metastases). MiR-21 expression, an important PDCD4 regulator, was assessed with real-time PCR analysis and showed inverse correlation to tissue PDCD4 expression.

Results: Nuclear and cytoplasmatic PDCD4 immunostaining decreased significantly with histopathological progression of the tumor (p<0001). Controls showed strong nuclear and cytoplasmatic immunohistochemical staining. MiR-21 up regulation in tissue corresponded to PDCD4 suppression.

Conclusions: These data support a decisive role for PDCD4 down regulation in transitional cell carcinoma and confirm miR-21 as a negative regulator for PDCD4. Additionally, PDCD4 immunohistochemical staining turns out to be a possible diagnostic marker for transitional cell carcinoma.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Apoptosis Regulatory Proteins / biosynthesis*
  • Carcinoma, Transitional Cell / metabolism*
  • Carcinoma, Transitional Cell / pathology
  • Female
  • Humans
  • Male
  • MicroRNAs / biosynthesis*
  • Middle Aged
  • Neoplasm Staging
  • Prognosis
  • RNA-Binding Proteins / biosynthesis*
  • Urologic Neoplasms / metabolism*
  • Urologic Neoplasms / pathology
  • Urothelium / metabolism*
  • Urothelium / pathology

Substances

  • Apoptosis Regulatory Proteins
  • MIRN21 microRNA, human
  • MicroRNAs
  • PDCD4 protein, human
  • RNA-Binding Proteins