Low expression of Mel-18 predicts poor prognosis in patients with breast cancer

Ann Oncol. 2010 Dec;21(12):2361-2369. doi: 10.1093/annonc/mdq241. Epub 2010 May 5.

Abstract

Background: Our previous study suggested that melanoma nuclear protein 18 (Mel-18) acted as a tumor suppressor in human breast cancer. This study was designed to investigate the clinical and prognostic significance of Mel-18 in breast cancer patients.

Patients and methods: Mel-18 was detected by immunohistochemistry in paraffin-embedded tissues from 287 breast cancer patients, of which 287 were from primary cancer sites, 63 from matched adjacent noncancerous sites, and 35 from metastatic lymph nodes. Differences in Mel-18 expression and clinical characteristics were compared by χ² test. Prognostic outcomes correlated with Mel-18 were examined using Kaplan-Meier analysis and Cox proportional hazards model.

Results: The decreased Mel-18 expression is incremental depending upon the magnitude of cancer progression (P < 0.001). Mel-18 was conversely correlated with the pathological classifications (P < 0.001 for T, N, and M classifications, respectively), clinical staging (P < 0.001), and progesterone receptor (P = 0.030). Furthermore, patients with higher level of Mel-18 showed prolonged overall survivals (P < 0.001). The diminished Mel-18 expression may be a risk factor for the patients' survival (P < 0.001).

Conclusions: Lower Mel-18 expression is correlated with advanced clinicopathologic classifications and a poor overall survival in breast cancer patients. These findings suggest that Mel-18 may serve as a useful marker in prognostic evaluation for patients.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Biomarkers, Tumor / analysis
  • Biomarkers, Tumor / metabolism
  • Breast Neoplasms / diagnosis*
  • Breast Neoplasms / metabolism
  • Breast Neoplasms / mortality*
  • Breast Neoplasms / pathology
  • Carcinoma / diagnosis*
  • Carcinoma / metabolism
  • Carcinoma / mortality*
  • Carcinoma / pathology
  • Case-Control Studies
  • Female
  • Humans
  • Middle Aged
  • Neoplasm Staging
  • Polycomb Repressive Complex 1
  • Prognosis
  • Repressor Proteins / analysis
  • Repressor Proteins / metabolism*
  • Survival Analysis

Substances

  • Biomarkers, Tumor
  • PCGF2 protein, human
  • Repressor Proteins
  • Polycomb Repressive Complex 1