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Establishment and Characterization of a CTC Cell Line from Peripheral Blood of Breast Cancer Patient

Background: Circulating tumor cell (CTC)-based patient-derived cells are ideal models for investigating the molecular basis of cancer. However, the rarity and heterogeneity of CTCs as well as the difficulties of primary culture limit their practical application. Establishing efficient in vitro cultu...

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Autores principales: Zhao, Pan, Zhou, Wenbin, Liu, Chang, Zhang, Huirong, Cheng, Zhiqiang, Wu, Weiqing, Liu, Kaisheng, Hu, Hong, Zhong, Caineng, Zhang, Yayuan, Zhou, Dongxian, Liu, Feiyuan, Dai, Yong, Wang, Jianhong, Zou, Chang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6856591/
https://www.ncbi.nlm.nih.gov/pubmed/31762819
http://dx.doi.org/10.7150/jca.33157
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author Zhao, Pan
Zhou, Wenbin
Liu, Chang
Zhang, Huirong
Cheng, Zhiqiang
Wu, Weiqing
Liu, Kaisheng
Hu, Hong
Zhong, Caineng
Zhang, Yayuan
Zhou, Dongxian
Liu, Feiyuan
Dai, Yong
Wang, Jianhong
Zou, Chang
author_facet Zhao, Pan
Zhou, Wenbin
Liu, Chang
Zhang, Huirong
Cheng, Zhiqiang
Wu, Weiqing
Liu, Kaisheng
Hu, Hong
Zhong, Caineng
Zhang, Yayuan
Zhou, Dongxian
Liu, Feiyuan
Dai, Yong
Wang, Jianhong
Zou, Chang
author_sort Zhao, Pan
collection PubMed
description Background: Circulating tumor cell (CTC)-based patient-derived cells are ideal models for investigating the molecular basis of cancer. However, the rarity and heterogeneity of CTCs as well as the difficulties of primary culture limit their practical application. Establishing efficient in vitro culture methods and functionally characterizing CTCs is essential for cancer studies. To this end, we developed an experimental protocol for the isolation, expansion, and identification of breast cancer CTCs. Methods: The CTC-3 cell line was established from peripheral blood cells of a breast cancer patient. A karyotype analysis was performed. The molecular profile was assessed by flow cytometry, quantitative real-time PCR, and western blot. The characteristics of tumors formed by CTC-3 cells were evaluated by cell growth and tumor sphere formation assays and in a mouse xenograft model. The tumors were analyzed by immunohistochemistry, immunofluorescence analysis, and hematoxylin and eosin staining. Results: The CTC-3 cell line showed more aggressive growth both in vitro and in vivo than the widely used MCF-7 breast cancer cell line. CTC-3 cells were also more resistant to chemotherapeutic agents, and gene profiling indicated higher expression levels of the epithelial-to-mesenchymal transition and stemness markers as compared to MCF-7 cells. Conclusions: CTC-3 cells are a better model for investigating the malignant behavior of breast cancer than existing cell lines.
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spelling pubmed-68565912019-11-24 Establishment and Characterization of a CTC Cell Line from Peripheral Blood of Breast Cancer Patient Zhao, Pan Zhou, Wenbin Liu, Chang Zhang, Huirong Cheng, Zhiqiang Wu, Weiqing Liu, Kaisheng Hu, Hong Zhong, Caineng Zhang, Yayuan Zhou, Dongxian Liu, Feiyuan Dai, Yong Wang, Jianhong Zou, Chang J Cancer Research Paper Background: Circulating tumor cell (CTC)-based patient-derived cells are ideal models for investigating the molecular basis of cancer. However, the rarity and heterogeneity of CTCs as well as the difficulties of primary culture limit their practical application. Establishing efficient in vitro culture methods and functionally characterizing CTCs is essential for cancer studies. To this end, we developed an experimental protocol for the isolation, expansion, and identification of breast cancer CTCs. Methods: The CTC-3 cell line was established from peripheral blood cells of a breast cancer patient. A karyotype analysis was performed. The molecular profile was assessed by flow cytometry, quantitative real-time PCR, and western blot. The characteristics of tumors formed by CTC-3 cells were evaluated by cell growth and tumor sphere formation assays and in a mouse xenograft model. The tumors were analyzed by immunohistochemistry, immunofluorescence analysis, and hematoxylin and eosin staining. Results: The CTC-3 cell line showed more aggressive growth both in vitro and in vivo than the widely used MCF-7 breast cancer cell line. CTC-3 cells were also more resistant to chemotherapeutic agents, and gene profiling indicated higher expression levels of the epithelial-to-mesenchymal transition and stemness markers as compared to MCF-7 cells. Conclusions: CTC-3 cells are a better model for investigating the malignant behavior of breast cancer than existing cell lines. Ivyspring International Publisher 2019-10-15 /pmc/articles/PMC6856591/ /pubmed/31762819 http://dx.doi.org/10.7150/jca.33157 Text en © The author(s) This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Zhao, Pan
Zhou, Wenbin
Liu, Chang
Zhang, Huirong
Cheng, Zhiqiang
Wu, Weiqing
Liu, Kaisheng
Hu, Hong
Zhong, Caineng
Zhang, Yayuan
Zhou, Dongxian
Liu, Feiyuan
Dai, Yong
Wang, Jianhong
Zou, Chang
Establishment and Characterization of a CTC Cell Line from Peripheral Blood of Breast Cancer Patient
title Establishment and Characterization of a CTC Cell Line from Peripheral Blood of Breast Cancer Patient
title_full Establishment and Characterization of a CTC Cell Line from Peripheral Blood of Breast Cancer Patient
title_fullStr Establishment and Characterization of a CTC Cell Line from Peripheral Blood of Breast Cancer Patient
title_full_unstemmed Establishment and Characterization of a CTC Cell Line from Peripheral Blood of Breast Cancer Patient
title_short Establishment and Characterization of a CTC Cell Line from Peripheral Blood of Breast Cancer Patient
title_sort establishment and characterization of a ctc cell line from peripheral blood of breast cancer patient
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6856591/
https://www.ncbi.nlm.nih.gov/pubmed/31762819
http://dx.doi.org/10.7150/jca.33157
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