Prognostic and metastatic value of phosphatase of regenerating liver-3 in invasive breast cancer

J Cancer Res Clin Oncol. 2010 Sep;136(9):1349-57. doi: 10.1007/s00432-010-0786-y. Epub 2010 Feb 6.

Abstract

Purpose: The aim of this study was to investigate the expression of the PRL-3 in human invasive breast cancer and to evaluate its clinical and prognostic significance. Its potential role in the invasive-metastatic properties of invasive breast cancer was also investigated.

Methods: Protein expression of PRL-3 was evaluated by immunohistochemistry for a consecutive series of 82 invasive human breast cancer tissues and 63 matched lymph node metastases, including PRL-3 mRNA expression analyzed by reverse transcriptase-polymerase chain reaction (RT-PCR) in malignant, nonmalignant breast tissue samples and lymph node metastases. We investigated the correlation of PRL-3 with clinicopathologic features, Overall and recurrence-free survival distribution curves were assessed using the Kaplan-Meier test and log-rank statistics, followed by Cox proportional hazards regression model.

Results: We found that 70.7% patients expressed a high level of PRL-3 protein in their tumors, and its over expression was positive correlated with lymph node metastasis (LNM) (P = 0.011). Moreover, The PRL-3 mRNA expression was significantly higher in malignant compared to benign breast tissue, while increased expression of PRL-3 mRNA was significantly associated with LNM (P = 0.002). Univariate analysis showed that the positive expression of PRL-3 was a poor risk prognostic factor (OS, P = 0.045; RFS, P = 0.034). Multivariate analysis using the Cox regression model indicated that high PRL-3 expression was an independent unfavorable prognostic factor for RFS.

Conclusions: These results strongly suggest that PRL-3 expression can indicate the potential role of LNM to some extent. Increasing the risk of tumor metastasis (OR = 3.889). Our results also imply that PRL-3 might be a novel molecular marker for predicting relapse of invasive breast cancer.

MeSH terms

  • Adult
  • Aged
  • Breast Neoplasms / diagnosis*
  • Breast Neoplasms / enzymology*
  • Breast Neoplasms / metabolism
  • Breast Neoplasms / pathology
  • Female
  • Humans
  • Immunohistochemistry
  • Lymphatic Metastasis / pathology
  • Middle Aged
  • Neoplasm Invasiveness / diagnosis
  • Neoplasm Proteins / biosynthesis
  • Neoplasm Proteins / metabolism*
  • Prognosis
  • Protein Tyrosine Phosphatases / biosynthesis
  • Protein Tyrosine Phosphatases / metabolism*
  • RNA, Messenger / biosynthesis
  • Recurrence
  • Reverse Transcriptase Polymerase Chain Reaction
  • Survival Analysis

Substances

  • Neoplasm Proteins
  • RNA, Messenger
  • PTP4A3 protein, human
  • Protein Tyrosine Phosphatases