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Detection and preliminary evaluation of circulating tumor cells in the peripheral blood of patients with eight types of cancer using a telomerase-specific adenovirus
We developed a detection method for circulating tumor cells (CTCs) using the telomerase-specific adenovirus OBP-401. This recombinant virus has a telomerase promoter at the 5′-end of the viral genome and GFP at the 3′-end. To date, CTC enumeration using OBP-401 has shown prognostic impact for gastri...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4203327/ https://www.ncbi.nlm.nih.gov/pubmed/25176113 http://dx.doi.org/10.3892/or.2014.3436 |
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author | YABUSAKI, MINA SATO, JUN KOHYAMA, ATSUSHI KOJIMA, TAKASHI NOBUOKA, DAISUKE YOSHIKAWA, TOSHIAKI SAWADA, YU MURAKAMI, KATSUHIRO GOHDA, KEIGO OKEGAWA, TAKATSUGU NAKAMURA, MASARU TAKAMATSU, KIYOSHI ITO, MASAAKI KANEKO, KAZUHIRO NAKATSURA, TETSUYA |
author_facet | YABUSAKI, MINA SATO, JUN KOHYAMA, ATSUSHI KOJIMA, TAKASHI NOBUOKA, DAISUKE YOSHIKAWA, TOSHIAKI SAWADA, YU MURAKAMI, KATSUHIRO GOHDA, KEIGO OKEGAWA, TAKATSUGU NAKAMURA, MASARU TAKAMATSU, KIYOSHI ITO, MASAAKI KANEKO, KAZUHIRO NAKATSURA, TETSUYA |
author_sort | YABUSAKI, MINA |
collection | PubMed |
description | We developed a detection method for circulating tumor cells (CTCs) using the telomerase-specific adenovirus OBP-401. This recombinant virus has a telomerase promoter at the 5′-end of the viral genome and GFP at the 3′-end. To date, CTC enumeration using OBP-401 has shown prognostic impact for gastric and small cell lung cancer patients. In the present study, peripheral blood samples from patients with eight types of cancer, including some cancers previously untested with OBP-401 (i.e., esophagus, pancreas, and prostate cancers) were subjected to this method in order to evaluate its versatility. It was recently discovered that some white blood cells (WBCs) false-positively react with OBP-401. Although anti-CD45 antibodies can absorb these adverse cells from peripheral blood, the simplicity of the OBP-401 method would be diminished by the introduction of antibody treatment. Therefore, we evaluated another approach to minimize the false positivity of WBCs. Seven anti-CD antibodies were employed to stain the species of WBCs that false-positively reacted with OBP-401. We revealed that the false-positively reacted WBCs were monocytes in the peripheral blood of both healthy subjects and cancer patients. Based on a size distribution analysis of the GFP-positive monocytes, the size criterion for CTCs using OBP-401 was defined to be a cellular diameter >8.4 μm. In total, 43% of 86 cancer patients examined in the present study were CTC-positive using this definition. CTCs were enumerated from peripheral blood samples collected from patients with each of the eight types of cancer; the detectability of CTCs for esophagus, pancreas and prostate cancers by the OBP-401 method was confirmed for the first time in the present study. However, no clear correlation between CTC positivity and the clinical characteristics of patients with any type of cancer was observed because of the small number of patients with each type of cancer. An additional clinical study will be conducted to confirm the clinical meaning of CTCs enumerated by OBP-401. |
format | Online Article Text |
id | pubmed-4203327 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-42033272014-10-21 Detection and preliminary evaluation of circulating tumor cells in the peripheral blood of patients with eight types of cancer using a telomerase-specific adenovirus YABUSAKI, MINA SATO, JUN KOHYAMA, ATSUSHI KOJIMA, TAKASHI NOBUOKA, DAISUKE YOSHIKAWA, TOSHIAKI SAWADA, YU MURAKAMI, KATSUHIRO GOHDA, KEIGO OKEGAWA, TAKATSUGU NAKAMURA, MASARU TAKAMATSU, KIYOSHI ITO, MASAAKI KANEKO, KAZUHIRO NAKATSURA, TETSUYA Oncol Rep Articles We developed a detection method for circulating tumor cells (CTCs) using the telomerase-specific adenovirus OBP-401. This recombinant virus has a telomerase promoter at the 5′-end of the viral genome and GFP at the 3′-end. To date, CTC enumeration using OBP-401 has shown prognostic impact for gastric and small cell lung cancer patients. In the present study, peripheral blood samples from patients with eight types of cancer, including some cancers previously untested with OBP-401 (i.e., esophagus, pancreas, and prostate cancers) were subjected to this method in order to evaluate its versatility. It was recently discovered that some white blood cells (WBCs) false-positively react with OBP-401. Although anti-CD45 antibodies can absorb these adverse cells from peripheral blood, the simplicity of the OBP-401 method would be diminished by the introduction of antibody treatment. Therefore, we evaluated another approach to minimize the false positivity of WBCs. Seven anti-CD antibodies were employed to stain the species of WBCs that false-positively reacted with OBP-401. We revealed that the false-positively reacted WBCs were monocytes in the peripheral blood of both healthy subjects and cancer patients. Based on a size distribution analysis of the GFP-positive monocytes, the size criterion for CTCs using OBP-401 was defined to be a cellular diameter >8.4 μm. In total, 43% of 86 cancer patients examined in the present study were CTC-positive using this definition. CTCs were enumerated from peripheral blood samples collected from patients with each of the eight types of cancer; the detectability of CTCs for esophagus, pancreas and prostate cancers by the OBP-401 method was confirmed for the first time in the present study. However, no clear correlation between CTC positivity and the clinical characteristics of patients with any type of cancer was observed because of the small number of patients with each type of cancer. An additional clinical study will be conducted to confirm the clinical meaning of CTCs enumerated by OBP-401. D.A. Spandidos 2014-11 2014-08-22 /pmc/articles/PMC4203327/ /pubmed/25176113 http://dx.doi.org/10.3892/or.2014.3436 Text en Copyright © 2014, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited. |
spellingShingle | Articles YABUSAKI, MINA SATO, JUN KOHYAMA, ATSUSHI KOJIMA, TAKASHI NOBUOKA, DAISUKE YOSHIKAWA, TOSHIAKI SAWADA, YU MURAKAMI, KATSUHIRO GOHDA, KEIGO OKEGAWA, TAKATSUGU NAKAMURA, MASARU TAKAMATSU, KIYOSHI ITO, MASAAKI KANEKO, KAZUHIRO NAKATSURA, TETSUYA Detection and preliminary evaluation of circulating tumor cells in the peripheral blood of patients with eight types of cancer using a telomerase-specific adenovirus |
title | Detection and preliminary evaluation of circulating tumor cells in the peripheral blood of patients with eight types of cancer using a telomerase-specific adenovirus |
title_full | Detection and preliminary evaluation of circulating tumor cells in the peripheral blood of patients with eight types of cancer using a telomerase-specific adenovirus |
title_fullStr | Detection and preliminary evaluation of circulating tumor cells in the peripheral blood of patients with eight types of cancer using a telomerase-specific adenovirus |
title_full_unstemmed | Detection and preliminary evaluation of circulating tumor cells in the peripheral blood of patients with eight types of cancer using a telomerase-specific adenovirus |
title_short | Detection and preliminary evaluation of circulating tumor cells in the peripheral blood of patients with eight types of cancer using a telomerase-specific adenovirus |
title_sort | detection and preliminary evaluation of circulating tumor cells in the peripheral blood of patients with eight types of cancer using a telomerase-specific adenovirus |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4203327/ https://www.ncbi.nlm.nih.gov/pubmed/25176113 http://dx.doi.org/10.3892/or.2014.3436 |
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