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Establishment and characterization of a patient-derived circulating lung tumor cell line in vitro and in vivo
BACKGROUND: Circulating tumor cells (CTCs) have been described as a population of cells that may seed metastasis, which is a reliable target for the prevention of metastases in lung cancer patients at the early stage. The culturing of CTCs in vitro can be used to study the mechanism of lung cancer m...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6352330/ https://www.ncbi.nlm.nih.gov/pubmed/30718976 http://dx.doi.org/10.1186/s12935-019-0735-z |
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author | Que, Zujun Luo, Bin Zhou, Zhiyi Dong, Changsheng Jiang, Yi Wang, Lin Shi, Qihui Tian, Jianhui |
author_facet | Que, Zujun Luo, Bin Zhou, Zhiyi Dong, Changsheng Jiang, Yi Wang, Lin Shi, Qihui Tian, Jianhui |
author_sort | Que, Zujun |
collection | PubMed |
description | BACKGROUND: Circulating tumor cells (CTCs) have been described as a population of cells that may seed metastasis, which is a reliable target for the prevention of metastases in lung cancer patients at the early stage. The culturing of CTCs in vitro can be used to study the mechanism of lung cancer metastasis and to screen antimetastasis drugs. This study aims to establish CTC cell line in vitro and explore the potential mechanism of its metastasis. METHODS: A mixture of EpCAM- and EGFR-coated immunomagnetic microbeads in microfluidic Herringbone-Chip was used to capture CTCs. The CTCs, 95-D and A549 cells was evaluated by cell proliferation assays, clonal formation assays, migration assays and drug resistance. Flow cytometry and cytokine protein chip were used to detect the difference in phenotype and cytokine secretion between CTCs, 95-D and A549 cells. The NOD/SCID mice were used to study tumorigenicity, lung organ colonization and metastasis of CTCs. The H&E staining, immunohistochemistry and immunofluorescence assay were used to detect the pathological status of CTCs. RESULTS: The number of EpCAM(+)/EGFR(+)/CK(+)/CD45(−) lung CTCs showed a weak negative correlation with clinical stages in patients with non-small cell lung cancer (NSCLC). In a phase IIa lung cancer patient, we successfully establish a permanent CTC cell line, named CTC-TJH-01. In vitro studies showed the CTC-TJH-01 cells were in the intermediate stage of epithelial to mesenchymal transition (EMT), had stem cell characteristics and were drug resistant. In vivo studies showed that CTC-TJH-01 cells can induce tumorigenesis, lung organ colonization and metastasis after xenografting in immunodeficient mice. In addition, the low expression level of CX3CL1 and high expression level of CXCL5 in the CTC-TJH-01 cells may be an important mechanism for their metastasis. CONCLUSIONS: We successfully established a permanent CTC cell line with metastatic ability, which can be used to screen antimetastatic drugs and study the mechanism of lung cancer metastasis. |
format | Online Article Text |
id | pubmed-6352330 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63523302019-02-04 Establishment and characterization of a patient-derived circulating lung tumor cell line in vitro and in vivo Que, Zujun Luo, Bin Zhou, Zhiyi Dong, Changsheng Jiang, Yi Wang, Lin Shi, Qihui Tian, Jianhui Cancer Cell Int Primary Research BACKGROUND: Circulating tumor cells (CTCs) have been described as a population of cells that may seed metastasis, which is a reliable target for the prevention of metastases in lung cancer patients at the early stage. The culturing of CTCs in vitro can be used to study the mechanism of lung cancer metastasis and to screen antimetastasis drugs. This study aims to establish CTC cell line in vitro and explore the potential mechanism of its metastasis. METHODS: A mixture of EpCAM- and EGFR-coated immunomagnetic microbeads in microfluidic Herringbone-Chip was used to capture CTCs. The CTCs, 95-D and A549 cells was evaluated by cell proliferation assays, clonal formation assays, migration assays and drug resistance. Flow cytometry and cytokine protein chip were used to detect the difference in phenotype and cytokine secretion between CTCs, 95-D and A549 cells. The NOD/SCID mice were used to study tumorigenicity, lung organ colonization and metastasis of CTCs. The H&E staining, immunohistochemistry and immunofluorescence assay were used to detect the pathological status of CTCs. RESULTS: The number of EpCAM(+)/EGFR(+)/CK(+)/CD45(−) lung CTCs showed a weak negative correlation with clinical stages in patients with non-small cell lung cancer (NSCLC). In a phase IIa lung cancer patient, we successfully establish a permanent CTC cell line, named CTC-TJH-01. In vitro studies showed the CTC-TJH-01 cells were in the intermediate stage of epithelial to mesenchymal transition (EMT), had stem cell characteristics and were drug resistant. In vivo studies showed that CTC-TJH-01 cells can induce tumorigenesis, lung organ colonization and metastasis after xenografting in immunodeficient mice. In addition, the low expression level of CX3CL1 and high expression level of CXCL5 in the CTC-TJH-01 cells may be an important mechanism for their metastasis. CONCLUSIONS: We successfully established a permanent CTC cell line with metastatic ability, which can be used to screen antimetastatic drugs and study the mechanism of lung cancer metastasis. BioMed Central 2019-01-29 /pmc/articles/PMC6352330/ /pubmed/30718976 http://dx.doi.org/10.1186/s12935-019-0735-z Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Primary Research Que, Zujun Luo, Bin Zhou, Zhiyi Dong, Changsheng Jiang, Yi Wang, Lin Shi, Qihui Tian, Jianhui Establishment and characterization of a patient-derived circulating lung tumor cell line in vitro and in vivo |
title | Establishment and characterization of a patient-derived circulating lung tumor cell line in vitro and in vivo |
title_full | Establishment and characterization of a patient-derived circulating lung tumor cell line in vitro and in vivo |
title_fullStr | Establishment and characterization of a patient-derived circulating lung tumor cell line in vitro and in vivo |
title_full_unstemmed | Establishment and characterization of a patient-derived circulating lung tumor cell line in vitro and in vivo |
title_short | Establishment and characterization of a patient-derived circulating lung tumor cell line in vitro and in vivo |
title_sort | establishment and characterization of a patient-derived circulating lung tumor cell line in vitro and in vivo |
topic | Primary Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6352330/ https://www.ncbi.nlm.nih.gov/pubmed/30718976 http://dx.doi.org/10.1186/s12935-019-0735-z |
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