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PC Cell-Derived Growth Factor Expression in Prostatic Intraepithelial Neoplasia and Prostatic Adenocarcinoma

  • Chong Xian Pan
  • , Michael S. Kinch
  • , Peter A. Kiener
  • , Solomon Langermann
  • , Ginette Serrero
  • , Le Sun
  • , Joseph Corvera
  • , Christopher J. Sweeney
  • , Lang Li
  • , Shaobo Zhang
  • , Lee Ann Baldridge
  • , Timothy D. Jones
  • , Michael O. Koch
  • , Thomas M. Ulbright
  • , John N. Eble
  • , Liang Cheng
  • Indiana University Bloomington
  • MedImmune, LLC
  • A and G Pharmaceuticals, Inc.

Research output: Contribution to journalArticlepeer-review

66 Scopus citations

Abstract

Purpose: PCDGF (PC cell-derived growth factor), also called progranulin, is a Mr 88,000 glycoprotein precursor of granulin. It is a novel growth factor that stimulates cell proliferation, confers epithelial tumorigenesis, and promotes tumor invasion. Here we investigate the potential of PCDGF as a therapeutic target for prostate cancer. Experimental Design: We studied the expression of PC-DGF in invasive prostate cancer, adjacent high-grade prostatic intraepithelial neoplasia (PIN), and benign prostate tissue from 99 human prostate specimens. The level of PC-DGF expression was correlated with various clinicopathological characteristics. Results: Normal prostate tissue did not express (53/99), or expressed low levels (46/99) of PCDGF. In the 46 normal prostate specimens that expressed PCDGF, most of them had less than 10% of cells expressing PCDGF. PCDGF expression could be detected in more than 50% of cells in all specimens of PIN and invasive prostate cancer. The expression of PCDGF in normal prostate tissue was much less intense and in a smaller fraction of cells than in PIN and invasive adenocarcinoma (P < 0.0001). There was no correlation of PCDGF expression with age, Gleason score, pathological stage, status of lymph node metastasis, extraprostatic extension, perineural invasion, surgical margins, and vascular invasion. Conclusions: Our data suggest that the induction of PCDGF expression occurs during the development of PIN. PCDGF may be a new molecular target for the treatment and prevention of prostate cancer.

Original languageEnglish
Pages (from-to)1333-1337
Number of pages5
JournalClinical Cancer Research
Volume10
Issue number4
DOIs
StatePublished - Feb 15 2004

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