Overexpression of Pleomorphic Adenoma Gene-Like 2 Is a Novel Poor Prognostic Marker of Prostate Cancer

PLoS One. 2016 Aug 18;11(8):e0158667. doi: 10.1371/journal.pone.0158667. eCollection 2016.

Abstract

Pleomorphic adenoma gene like-2 (PLAGL2) is a member of the PLAG gene family. Previous studies have revealed that overexpression of PLAGL2 is associated with many human cancers. However, it has been reported that PLAGL2 also plays as a tumor suppressor. The precise role of PLAGL2 in prostate cancer (PCa) is still unknown. The aim of this study was to investigate the expression and prognostic value of PLAGL2 in PCa. Data from microarray datasets demonstrated that the DNA copy number and mRNA level of PLAGL2 were significantly increased in PCa compared with normal prostate. qRT-PCR and western blot analysis from paired PCa samples and prostate cell lines confirmed upregulated mRNA and protein expression levels in PCa. Immunohistochemistry analysis showed that staining of PLAGL2 in PCa tissues was significantly higher than that in benign prostatic hyperplasia (BPH) tissues. In addition, the high expression of PLAGL2 was only involved in preoperative PSA, but was not related to age, Gleason score, seminal vesicle invasion, surgical margin status, clinical stage and positive lymph node metastasis. Moreover, our results showed that PLAGL2 was an independent prognostic factor for biochemical recurrence (BCR)-free survival and overall survival (OS) of PCa patients, and overexpressed PLAGL2 was related to early development of BCR and poor OS. In conclusion, our findings suggest that PLAGL2 is overexpressed in PCa. The increased expression of PLAGL2 correlates to PCa progression following radical prostatectomy and may serve as a novel poor prognostic marker for PCa.

MeSH terms

  • Biomarkers, Tumor / analysis
  • Blotting, Western
  • Cell Line, Tumor
  • DNA-Binding Proteins / analysis*
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Kaplan-Meier Estimate
  • Male
  • Middle Aged
  • Oligonucleotide Array Sequence Analysis
  • Prognosis
  • Prostate / chemistry
  • Prostate-Specific Antigen / blood
  • Prostatic Hyperplasia / diagnosis
  • Prostatic Neoplasms / chemistry
  • Prostatic Neoplasms / diagnosis*
  • Prostatic Neoplasms / mortality
  • RNA-Binding Proteins / analysis*
  • Real-Time Polymerase Chain Reaction
  • Survival Analysis
  • Transcription Factors / analysis*

Substances

  • Biomarkers, Tumor
  • DNA-Binding Proteins
  • PLAGL2 protein, human
  • RNA-Binding Proteins
  • Transcription Factors
  • Prostate-Specific Antigen

Grants and funding

This study is supported by the grants from the National Natural Science Foundation of China (No.2013RMFH012), the Province Natural Science Foundation of Hubei (No.2012FFA096), the Science Foundation of Wuhan (NO. 2015060101010049) and supported by the Fundamental Research Funds for the Central Universities (NO. 2042014kf0115).