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Characteristics of circulating tumor cells in organ metastases, prognosis, and T lymphocyte mediated immune response

Circulating tumor cells (CTCs) possess profound influence on tumor metastases and disease progression. This study aimed to investigate the correlation of CTCs with clinical characteristics and T-cell immunity, and to explore whether CTCs and the subpopulations can serve as an independent prognostic...

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Autores principales: Sun, Wen-Wen, Xu, Zhi-Hong, Lian, Peng, Gao, Bei-Li, Hu, Jia-An
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5422503/
https://www.ncbi.nlm.nih.gov/pubmed/28496340
http://dx.doi.org/10.2147/OTT.S130087
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author Sun, Wen-Wen
Xu, Zhi-Hong
Lian, Peng
Gao, Bei-Li
Hu, Jia-An
author_facet Sun, Wen-Wen
Xu, Zhi-Hong
Lian, Peng
Gao, Bei-Li
Hu, Jia-An
author_sort Sun, Wen-Wen
collection PubMed
description Circulating tumor cells (CTCs) possess profound influence on tumor metastases and disease progression. This study aimed to investigate the correlation of CTCs with clinical characteristics and T-cell immunity, and to explore whether CTCs and the subpopulations can serve as an independent prognostic factor in advanced non-small cell lung cancer (NSCLC). A prospective study was conducted in late stages of NSCLC patients. The levels of overall CTCs and the three subpopulation CTCs were enumerated using the CanPatrol™ CTC enrichment system. The information about the patients which included the clinical characteristics, survival status at the 200th day postdiagnosis, and the levels of T cells was collected. Mann–Whitney U test, Kruskal–Wallis H test, Cox regression, and Spearman’s rank correlation coefficient were the statistical methods used in this study. We detected CTCs in 27 of the 31 eligible patients; the level of epithelial–mesenchymal circulating tumor cells (EMCTCs) was higher than that of epithelial circulating tumor cells and that of mesenchymal circulating tumor cells (MCTCs) in the majority of NSCLC patients. Organ metastases were positively associated with the levels of overall CTCs, EMCTCs, and MCTCs (P<0.05). EMCTCs and MCTCs were associated with worse clinical outcomes. Additionally, the levels of EMCTCs were negatively associated with the levels of CD3(+) T cells (P=0.01) and CD8(+) T cells (P=0.04). In conclusion, the levels of CTCs were positively associated with organ metastases, particularly bone metastases, but were negatively associated with T-cell levels. The levels of EMCTCs and MCTCs had negative prognostic value.
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spelling pubmed-54225032017-05-11 Characteristics of circulating tumor cells in organ metastases, prognosis, and T lymphocyte mediated immune response Sun, Wen-Wen Xu, Zhi-Hong Lian, Peng Gao, Bei-Li Hu, Jia-An Onco Targets Ther Original Research Circulating tumor cells (CTCs) possess profound influence on tumor metastases and disease progression. This study aimed to investigate the correlation of CTCs with clinical characteristics and T-cell immunity, and to explore whether CTCs and the subpopulations can serve as an independent prognostic factor in advanced non-small cell lung cancer (NSCLC). A prospective study was conducted in late stages of NSCLC patients. The levels of overall CTCs and the three subpopulation CTCs were enumerated using the CanPatrol™ CTC enrichment system. The information about the patients which included the clinical characteristics, survival status at the 200th day postdiagnosis, and the levels of T cells was collected. Mann–Whitney U test, Kruskal–Wallis H test, Cox regression, and Spearman’s rank correlation coefficient were the statistical methods used in this study. We detected CTCs in 27 of the 31 eligible patients; the level of epithelial–mesenchymal circulating tumor cells (EMCTCs) was higher than that of epithelial circulating tumor cells and that of mesenchymal circulating tumor cells (MCTCs) in the majority of NSCLC patients. Organ metastases were positively associated with the levels of overall CTCs, EMCTCs, and MCTCs (P<0.05). EMCTCs and MCTCs were associated with worse clinical outcomes. Additionally, the levels of EMCTCs were negatively associated with the levels of CD3(+) T cells (P=0.01) and CD8(+) T cells (P=0.04). In conclusion, the levels of CTCs were positively associated with organ metastases, particularly bone metastases, but were negatively associated with T-cell levels. The levels of EMCTCs and MCTCs had negative prognostic value. Dove Medical Press 2017-05-04 /pmc/articles/PMC5422503/ /pubmed/28496340 http://dx.doi.org/10.2147/OTT.S130087 Text en © 2017 Sun et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Sun, Wen-Wen
Xu, Zhi-Hong
Lian, Peng
Gao, Bei-Li
Hu, Jia-An
Characteristics of circulating tumor cells in organ metastases, prognosis, and T lymphocyte mediated immune response
title Characteristics of circulating tumor cells in organ metastases, prognosis, and T lymphocyte mediated immune response
title_full Characteristics of circulating tumor cells in organ metastases, prognosis, and T lymphocyte mediated immune response
title_fullStr Characteristics of circulating tumor cells in organ metastases, prognosis, and T lymphocyte mediated immune response
title_full_unstemmed Characteristics of circulating tumor cells in organ metastases, prognosis, and T lymphocyte mediated immune response
title_short Characteristics of circulating tumor cells in organ metastases, prognosis, and T lymphocyte mediated immune response
title_sort characteristics of circulating tumor cells in organ metastases, prognosis, and t lymphocyte mediated immune response
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5422503/
https://www.ncbi.nlm.nih.gov/pubmed/28496340
http://dx.doi.org/10.2147/OTT.S130087
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