To the top

Page Manager: Webmaster
Last update: 9/11/2012 3:13 PM

Tell a friend about this page
Print version

Filtration-based enrichme… - University of Gothenburg, Sweden Till startsida
Sitemap
To content Read more about how we use cookies on gu.se

Filtration-based enrichment of circulating tumor cells from all prostate cancer risk groups

Journal article
Authors Julius Adebayo Awe
J. Saranchuk
D. Drachenberg
S. Mai
Published in Urologic Oncology-Seminars and Original Investigations
Volume 35
Issue 5
Pages 300-309
ISSN 1078-1439
Publication year 2017
Published at Institute of Biomedicine, Department of Medical and Clinical Genetics
Pages 300-309
Language en
Links 10.1016/j.urolonc.2016.12.008
Keywords Prostate cancer, Circulating tumor cells, Androgen receptors, Cytokeratin, Filter isolation, adenocarcinoma, metastasis, survival, size
Subject categories Cancer and Oncology

Abstract

Objective: To combine circulating tumor cell (CTC) isolation by filtration and immunohistochemistry to investigate the presence of CTCs in low, intermediate, and high-risk prostate cancer (PCa). CTCs isolated from these risk groups stained positive for both cytokeratin and androgen receptors, but negative for CD45. Patients and methods: Blood samples from 41 biopsy confirmed patients with PCa at different clinical stages such as low, intermediate, and high risk were analyzed. The samples were processed with the ScreenCell filtration device and PCa CTCs were captured for all patients. The isolated CTCs were confirmed PCa CTCs by the presence of androgen receptors and cytokeratins 8, 18, and 19 that occurred in the absence of CD45 positivity. PCa CTC nuclear sizes were measured using the TeloView program. Results: The filtration-based isolation method used permitted the measurement of the average nuclear size of the captured CTCs. CTCs were identified by immunohistochemistry in low, intermediate, and high-risk groups of patients with PCa. Conclusion: CTCs may be found in all stages of PCa. These CTCs can be used to determine the level of genomic instability at any stage of PCa; this will, in the future, enable personalized patient management. (C) 2017 The Authors. Published by Elsevier Inc.

Page Manager: Webmaster|Last update: 9/11/2012
Share:

The University of Gothenburg uses cookies to provide you with the best possible user experience. By continuing on this website, you approve of our use of cookies.  What are cookies?