Skip to main navigation Skip to search Skip to main content

p53 in cutaneous melanoma: Immunoreactivity and correlation with prognosis

  • University of Melbourne
  • St. Vincent's Hospital Melbourne
  • Austin Health

Research output: Contribution to journalArticlepeer-review

15 Citations (Scopus)

Abstract

p53 protein immunoreactivity was investigated in cutaneous Spitz naevi (n= 7), superficial spreading (n= 21) and nodular (n= 6) melanomas using the monoclonal antibody DO‐7. Nuclear immunostaining for p53 protein was observed in 41% of all the melanomas but not in any of the Spitz naevi studied. This difference in p53 immunoreactivity appeared statistically significant (P= 0.0001; χ2 test). There were also differences in p53 immunoreactivity between superficial spreading and nodular melanomas (P= 0.001, χ2 test), where up to 38% of superficial spreading melanomas and 50% of nodular melanomas had demonstrated p53 nuclear immunostaining. An apparently significant correlation was observed between melanomas with poor prognostic histological indices and p53 immunoreactivity (P= 0.0016; χ2 test). In conclusion, increased p53 protein immunoreactivity is found in melanomas and is associated with poorer prognosis. The differences in p53 immunohistological expression between cutaneous melanomas and Spitz naevi suggest that alterations of the protein may be important in the pathogenesis of the tumour.

Original languageEnglish
Pages (from-to)192-195
Number of pages4
JournalAustralasian Journal of Dermatology
Volume36
Issue number4
DOIs
Publication statusPublished - Nov 1995
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • DO‐7
  • immunohistochemistry
  • Spitz naevus
  • tumour suppressor gene

Fingerprint

Dive into the research topics of 'p53 in cutaneous melanoma: Immunoreactivity and correlation with prognosis'. Together they form a unique fingerprint.

Cite this