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Circulating Tumor Cell Detection in Lung Cancer Animal Model
BACKGROUND: Metastasis and recurrence of primary cancer are the main causes of cancer mortality. Disseminated tumor cells refer to cancer cells that cause metastasis from primary cancer to other organs. Several recent studies have suggested that circulating tumor cells (CTCs) are associated with the...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Korean Society for Thoracic and Cardiovascular Surgery
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8646057/ https://www.ncbi.nlm.nih.gov/pubmed/34667135 http://dx.doi.org/10.5090/jcs.21.044 |
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author | Chong, Yooyoung Jung, Yong Chae Hwang, Euidoo Cho, Hyun Jin Kang, Min-Woong Na, Myung Hoon |
author_facet | Chong, Yooyoung Jung, Yong Chae Hwang, Euidoo Cho, Hyun Jin Kang, Min-Woong Na, Myung Hoon |
author_sort | Chong, Yooyoung |
collection | PubMed |
description | BACKGROUND: Metastasis and recurrence of primary cancer are the main causes of cancer mortality. Disseminated tumor cells refer to cancer cells that cause metastasis from primary cancer to other organs. Several recent studies have suggested that circulating tumor cells (CTCs) are associated with the clinical stage, cancer recurrence, cancer metastasis, and prognosis. There are several methods of isolating CTCs from whole blood; in particular, using a membrane filtration system is advantageous due to its cost-effectiveness and availability in clinical settings. In this study, an animal model of lung cancer was established in nude mice using the human large cell lung cancer cell line H460. METHODS: Six-week-old nude mice were used. The H460 lung cancer cell line was injected subcutaneously into the nude mice. Blood samples were obtained from the orbital area before cell line injection, 2 weeks after injection, and 2 weeks after tumor excision. Blood samples were filtered using a polycarbonate 12-well Transwell membrane (Corning Inc., Corning, NY, USA). An indirect immunofluorescence assay was performed with the epithelial cell adhesion molecule antibody. The number of stained cells was counted using fluorescence microscopy. RESULTS: The average size of the tumor masses was 35.83 mm. The stained cells were counted before inoculation, 2 weeks after inoculation, and 2 weeks after tumor excision. Cancer cells generally increased after inoculation and decreased after tumor resection. CONCLUSION: The CTC detection method using the commercial polycarbonate 12-well Transwell (Corning Inc.) membrane is advantageous in terms of cost-effectiveness and convenience. |
format | Online Article Text |
id | pubmed-8646057 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Korean Society for Thoracic and Cardiovascular Surgery |
record_format | MEDLINE/PubMed |
spelling | pubmed-86460572021-12-15 Circulating Tumor Cell Detection in Lung Cancer Animal Model Chong, Yooyoung Jung, Yong Chae Hwang, Euidoo Cho, Hyun Jin Kang, Min-Woong Na, Myung Hoon J Chest Surg Basic Research BACKGROUND: Metastasis and recurrence of primary cancer are the main causes of cancer mortality. Disseminated tumor cells refer to cancer cells that cause metastasis from primary cancer to other organs. Several recent studies have suggested that circulating tumor cells (CTCs) are associated with the clinical stage, cancer recurrence, cancer metastasis, and prognosis. There are several methods of isolating CTCs from whole blood; in particular, using a membrane filtration system is advantageous due to its cost-effectiveness and availability in clinical settings. In this study, an animal model of lung cancer was established in nude mice using the human large cell lung cancer cell line H460. METHODS: Six-week-old nude mice were used. The H460 lung cancer cell line was injected subcutaneously into the nude mice. Blood samples were obtained from the orbital area before cell line injection, 2 weeks after injection, and 2 weeks after tumor excision. Blood samples were filtered using a polycarbonate 12-well Transwell membrane (Corning Inc., Corning, NY, USA). An indirect immunofluorescence assay was performed with the epithelial cell adhesion molecule antibody. The number of stained cells was counted using fluorescence microscopy. RESULTS: The average size of the tumor masses was 35.83 mm. The stained cells were counted before inoculation, 2 weeks after inoculation, and 2 weeks after tumor excision. Cancer cells generally increased after inoculation and decreased after tumor resection. CONCLUSION: The CTC detection method using the commercial polycarbonate 12-well Transwell (Corning Inc.) membrane is advantageous in terms of cost-effectiveness and convenience. The Korean Society for Thoracic and Cardiovascular Surgery 2021-12-05 2021-10-20 /pmc/articles/PMC8646057/ /pubmed/34667135 http://dx.doi.org/10.5090/jcs.21.044 Text en Copyright © 2021, The Korean Society for Thoracic and Cardiovascular Surgery https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Basic Research Chong, Yooyoung Jung, Yong Chae Hwang, Euidoo Cho, Hyun Jin Kang, Min-Woong Na, Myung Hoon Circulating Tumor Cell Detection in Lung Cancer Animal Model |
title | Circulating Tumor Cell Detection in Lung Cancer Animal Model |
title_full | Circulating Tumor Cell Detection in Lung Cancer Animal Model |
title_fullStr | Circulating Tumor Cell Detection in Lung Cancer Animal Model |
title_full_unstemmed | Circulating Tumor Cell Detection in Lung Cancer Animal Model |
title_short | Circulating Tumor Cell Detection in Lung Cancer Animal Model |
title_sort | circulating tumor cell detection in lung cancer animal model |
topic | Basic Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8646057/ https://www.ncbi.nlm.nih.gov/pubmed/34667135 http://dx.doi.org/10.5090/jcs.21.044 |
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