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Clinical significance of glypican-3-positive circulating tumor cells of hepatocellular carcinoma patients: A prospective study

The utility of glypican-3 (GPC3) expression for the detection of circulating tumor cells (CTCs) in hepatocellular carcinoma (HCC) patients has not been elucidated. The aim of this study was to identify associations between the presence of GPC3-positive CTCs and clinicopathological factors of these p...

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Autores principales: Hamaoka, Michinori, Kobayashi, Tsuyoshi, Tanaka, Yuka, Mashima, Hiroaki, Ohdan, Hideki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6541303/
https://www.ncbi.nlm.nih.gov/pubmed/31141571
http://dx.doi.org/10.1371/journal.pone.0217586
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author Hamaoka, Michinori
Kobayashi, Tsuyoshi
Tanaka, Yuka
Mashima, Hiroaki
Ohdan, Hideki
author_facet Hamaoka, Michinori
Kobayashi, Tsuyoshi
Tanaka, Yuka
Mashima, Hiroaki
Ohdan, Hideki
author_sort Hamaoka, Michinori
collection PubMed
description The utility of glypican-3 (GPC3) expression for the detection of circulating tumor cells (CTCs) in hepatocellular carcinoma (HCC) patients has not been elucidated. The aim of this study was to identify associations between the presence of GPC3-positive CTCs and clinicopathological factors of these patients, furthermore, to evaluate whether CTC can predict microscopic portal vein invasion (mPVI). This study was done on 85 patients who underwent hepatectomy as the first-line treatment and whose preoperative imaging showed no evidence of macroscopic PVI and distant metastases. Peripheral blood was collected from all patients immediately before surgery. Cells were purified initially by density gradient centrifugation followed by immunomagnetic positive enrichment based upon the expression of GPC3. The numbers of CTCs contained in the enriched samples were enumerated via flow cytometry. Protocol validation using HepG2 cells spiked into 8.0 mL of blood from a healthy volunteer indicated that we were able to recover 12.1% of the tumor cells. A median number of 3 CTCs (range: 0–27) was detected in the 8.0 mL of peripheral blood of the 85 analyzed HCC patients. Thirty-three patients had CTCs ≥5, and these patients had a higher incidence of mPVI (p < 0.001), a lower disease-free survival (p = 0.015), and a lower overall survival (p = 0.047) than those with CTCs <5. Multivariate analysis identified CTCs ≥5 as an independent predictor of mPVI (p < 0.001). In conclusion, preoperative GPC3-positive CTCs ≥5 was a risk factor of mPVI and poor prognosis, and therefore may be a useful biomarker for HCC patient outcomes.
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spelling pubmed-65413032019-06-05 Clinical significance of glypican-3-positive circulating tumor cells of hepatocellular carcinoma patients: A prospective study Hamaoka, Michinori Kobayashi, Tsuyoshi Tanaka, Yuka Mashima, Hiroaki Ohdan, Hideki PLoS One Research Article The utility of glypican-3 (GPC3) expression for the detection of circulating tumor cells (CTCs) in hepatocellular carcinoma (HCC) patients has not been elucidated. The aim of this study was to identify associations between the presence of GPC3-positive CTCs and clinicopathological factors of these patients, furthermore, to evaluate whether CTC can predict microscopic portal vein invasion (mPVI). This study was done on 85 patients who underwent hepatectomy as the first-line treatment and whose preoperative imaging showed no evidence of macroscopic PVI and distant metastases. Peripheral blood was collected from all patients immediately before surgery. Cells were purified initially by density gradient centrifugation followed by immunomagnetic positive enrichment based upon the expression of GPC3. The numbers of CTCs contained in the enriched samples were enumerated via flow cytometry. Protocol validation using HepG2 cells spiked into 8.0 mL of blood from a healthy volunteer indicated that we were able to recover 12.1% of the tumor cells. A median number of 3 CTCs (range: 0–27) was detected in the 8.0 mL of peripheral blood of the 85 analyzed HCC patients. Thirty-three patients had CTCs ≥5, and these patients had a higher incidence of mPVI (p < 0.001), a lower disease-free survival (p = 0.015), and a lower overall survival (p = 0.047) than those with CTCs <5. Multivariate analysis identified CTCs ≥5 as an independent predictor of mPVI (p < 0.001). In conclusion, preoperative GPC3-positive CTCs ≥5 was a risk factor of mPVI and poor prognosis, and therefore may be a useful biomarker for HCC patient outcomes. Public Library of Science 2019-05-29 /pmc/articles/PMC6541303/ /pubmed/31141571 http://dx.doi.org/10.1371/journal.pone.0217586 Text en © 2019 Hamaoka et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Hamaoka, Michinori
Kobayashi, Tsuyoshi
Tanaka, Yuka
Mashima, Hiroaki
Ohdan, Hideki
Clinical significance of glypican-3-positive circulating tumor cells of hepatocellular carcinoma patients: A prospective study
title Clinical significance of glypican-3-positive circulating tumor cells of hepatocellular carcinoma patients: A prospective study
title_full Clinical significance of glypican-3-positive circulating tumor cells of hepatocellular carcinoma patients: A prospective study
title_fullStr Clinical significance of glypican-3-positive circulating tumor cells of hepatocellular carcinoma patients: A prospective study
title_full_unstemmed Clinical significance of glypican-3-positive circulating tumor cells of hepatocellular carcinoma patients: A prospective study
title_short Clinical significance of glypican-3-positive circulating tumor cells of hepatocellular carcinoma patients: A prospective study
title_sort clinical significance of glypican-3-positive circulating tumor cells of hepatocellular carcinoma patients: a prospective study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6541303/
https://www.ncbi.nlm.nih.gov/pubmed/31141571
http://dx.doi.org/10.1371/journal.pone.0217586
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