Detection and phenotyping of circulating tumor cells in high-risk localized prostate cancer

Clin Genitourin Cancer. 2015 Apr;13(2):130-6. doi: 10.1016/j.clgc.2014.08.014. Epub 2014 Sep 22.

Abstract

Background: In this study, we aimed to determine the feasibility of identifying CTCs in patients with HRLPC, using a modified isolation procedure using the CellSearch (Veridex) platform, and to assess the expression of stem cell and epithelial-mesenchymal transition (EMT) markers on the CTCs.

Patients and methods: Thirty-five patients with HRLPC who had chosen prostatectomy for definitive management were prospectively identified. After obtaining consent, four 30-mL blood draws were performed, 2 before surgery and 2 after surgery. The CTC-containing fraction was Ficoll-purified and transferred to a CellSave (Veridex) tube containing dilution buffer before standard enumeration using the CellSearch system. Loss of E-cadherin expression, a marker of EMT, and CD133, a putative prostate cancer stem cell marker, were characterized using the open channel of the CellSearch platform. CTC fragments were also enumerated.

Results: Using the modified methodology, CTCs were detectable in 49% of patients before surgery. Although no correlation between CTC count and biochemical recurrence (BR) was observed, the percentages of CD133 and E-cadherin-positive CTC fragments were associated with BR at 1 year.

Conclusion: Our results suggest that further research into the development of CTCs as prognostic biomarkers in HRLPC is warranted.

Keywords: CD133; CellSearch; EMT; Fragment; Stem cell.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • AC133 Antigen
  • Aged
  • Antigens, CD / metabolism*
  • Biomarkers, Tumor / metabolism*
  • Cadherins / metabolism*
  • Cell Count
  • Cell Separation / methods
  • Epithelial-Mesenchymal Transition
  • Feasibility Studies
  • Glycoproteins / metabolism*
  • Humans
  • Male
  • Middle Aged
  • Neoplastic Cells, Circulating / metabolism
  • Neoplastic Cells, Circulating / pathology*
  • Peptides / metabolism*
  • Phenotype
  • Prognosis
  • Prospective Studies
  • Prostatic Neoplasms / blood
  • Prostatic Neoplasms / pathology*

Substances

  • AC133 Antigen
  • Antigens, CD
  • Biomarkers, Tumor
  • Cadherins
  • Glycoproteins
  • PROM1 protein, human
  • Peptides