Expression of glucose-regulated stress protein GRP78 is related to progression of melanoma

  • Liquing Zhuang
  • , Richard A. Scolyer
  • , C. Soon Lee
  • , Stanley W. McCarthy
  • , Wendy A. Cooper
  • , Xu D. Zhang
  • , John F. Thompson
  • , Peter Hersey

Research output: Contribution to journalArticlepeer-review

94 Citations (Scopus)

Abstract

Glucose-regulated protein 78 (GRP78) is a protein translated in response to endoplasmic reticulum (ER) stress that has been implicated in the pathogenesis and resistance to therapy of a variety of cancers. The aim of this study was to investigate its expression and role in the development and progression of human melanoma. The immunohistochemical expression of GRP78 in naevi, primary melanoma and melanoma metastases from 171 patients was correlated with clinicopathological factors and patient survival. The GRP78 immunoreactivity score (IRS) was 0.2 in compound naevi, 0.65 in dysplastic naevi, 4.65 in naevi adjacent to primary melanoma, 2.4 in melanoma in situ, 11.2 in thin (£1.0 mm) and 18.1 in thick (>1.0 mm) primary melanoma. It was 18 and 17.3 in subcutaneous and lymph node metastases, respectively (P < 0.0001). GRP78 expression was positively correlated with increasing tumour thickness (P = 0.001) and with increasing dermal tumour mitotic index (P = 0.0004). Disease-free survival (v2 = 8.0703, P = 0.0045) and overall survival (v2 = 6.2633, P = 0.0123) in melanoma patients with IRS >25 were significantly lower than in melanoma patients with IRS <25. GRP78 expression appears to correlate with known correlates of melanoma progression and survival and requires further evaluation as a prognostic biomarker in melanoma.
Original languageEnglish
Pages (from-to)462-470
Number of pages9
JournalHistopathology
Volume54
Issue number4
DOIs
Publication statusPublished - 2009

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

  • endoplasmic reticulum
  • melanocytic lesions
  • melanoma
  • pathogenesis
  • stress protein

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