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.
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Authors | Sumanta K Pal, Miaoling He, Timothy Wilson, Xueli Liu, Keqiang Zhang, Courtney Carmichael, Alejandra Torres, Sonya Hernandez, Clayton Lau, Neeraj Agarwal, Mark Kawachi, Yun Yen, Jeremy O Jones |
Journal | Clinical genitourinary cancer
(Clin Genitourin Cancer)
Vol. 13
Issue 2
Pg. 130-6
(Apr 2015)
ISSN: 1938-0682 [Electronic] United States |
PMID | 25450039
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2015 Elsevier Inc. All rights reserved. |
Chemical References |
- AC133 Antigen
- Antigens, CD
- Biomarkers, Tumor
- Cadherins
- Glycoproteins
- PROM1 protein, human
- Peptides
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Topics |
- 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, pathology)
- Peptides
(metabolism)
- Phenotype
- Prognosis
- Prospective Studies
- Prostatic Neoplasms
(blood, pathology)
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