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Establishment of rat liver cancer cell lines with different metastatic potential

The gloomy outcome of liver cancer is mainly due to the high rates of metastasis and recurrence, even after curative resection for early stage liver cancer. Our study was conducted to find the animal model suitable for the study of liver cancer metastasis. In our study, two liver cancer cells were o...

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Autores principales: Song, Lei, Zhang, Jian-gang, Zheng, Long, Feng, Xu, Hou, Jie, Zhang, Huan-ling, Liu, Shu-feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7239898/
https://www.ncbi.nlm.nih.gov/pubmed/32433581
http://dx.doi.org/10.1038/s41598-020-65338-w
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author Song, Lei
Zhang, Jian-gang
Zheng, Long
Feng, Xu
Hou, Jie
Zhang, Huan-ling
Liu, Shu-feng
author_facet Song, Lei
Zhang, Jian-gang
Zheng, Long
Feng, Xu
Hou, Jie
Zhang, Huan-ling
Liu, Shu-feng
author_sort Song, Lei
collection PubMed
description The gloomy outcome of liver cancer is mainly due to the high rates of metastasis and recurrence, even after curative resection for early stage liver cancer. Our study was conducted to find the animal model suitable for the study of liver cancer metastasis. In our study, two liver cancer cells were obtained from N-nitrosodiethylamine (DEN) and N-nitrosomorpholine (NMOR) induced rats, and they were cultivated, screened and cloning cultivated. Bionomics of cells was analyzed. The results show that 2 cells had different metastatic potentiality. They were named Wrh-f2 and Wrh-s2, and they have the characteristics of Hepatocellular carcinoma cells. The bionomics of 2 cells showed: (1) The chromosome karyotype analysis showed that the mode of Wrh-f2 was 80–83 and Wrh-s2 was 55–57; (2) AFP positive cytoplasmic staining was observed in Wrh-f2 and Wrh-s2. Cytokeratin (CK) 7 and CK8 positive staining was present in Wrh-f2. CK8 positive staining was present in Wrh-s2; (3) The numbers of Wrh-f2 and Wrh-s2 that passed through the Transwells were 98 ± 12 and 55 ± 15;(4) Wrh-f2 had the significant higher colony formation (78%) than Wrh-s2(8%) (P < 0.01). (5) The animal models generated solid tumours when 2 cells were inoculated to nude mouse and rat. And Wrh-f2 developed stable pulmonary metastasis. The established cell lines with different metastatic potential showed obvious advantages over liver cancer in mimicking the biological properties of malignant liver cancer tumors. It provided a suitable model for the mechanism of liver cancer metastasis in vivo and in vitro.
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spelling pubmed-72398982020-05-29 Establishment of rat liver cancer cell lines with different metastatic potential Song, Lei Zhang, Jian-gang Zheng, Long Feng, Xu Hou, Jie Zhang, Huan-ling Liu, Shu-feng Sci Rep Article The gloomy outcome of liver cancer is mainly due to the high rates of metastasis and recurrence, even after curative resection for early stage liver cancer. Our study was conducted to find the animal model suitable for the study of liver cancer metastasis. In our study, two liver cancer cells were obtained from N-nitrosodiethylamine (DEN) and N-nitrosomorpholine (NMOR) induced rats, and they were cultivated, screened and cloning cultivated. Bionomics of cells was analyzed. The results show that 2 cells had different metastatic potentiality. They were named Wrh-f2 and Wrh-s2, and they have the characteristics of Hepatocellular carcinoma cells. The bionomics of 2 cells showed: (1) The chromosome karyotype analysis showed that the mode of Wrh-f2 was 80–83 and Wrh-s2 was 55–57; (2) AFP positive cytoplasmic staining was observed in Wrh-f2 and Wrh-s2. Cytokeratin (CK) 7 and CK8 positive staining was present in Wrh-f2. CK8 positive staining was present in Wrh-s2; (3) The numbers of Wrh-f2 and Wrh-s2 that passed through the Transwells were 98 ± 12 and 55 ± 15;(4) Wrh-f2 had the significant higher colony formation (78%) than Wrh-s2(8%) (P < 0.01). (5) The animal models generated solid tumours when 2 cells were inoculated to nude mouse and rat. And Wrh-f2 developed stable pulmonary metastasis. The established cell lines with different metastatic potential showed obvious advantages over liver cancer in mimicking the biological properties of malignant liver cancer tumors. It provided a suitable model for the mechanism of liver cancer metastasis in vivo and in vitro. Nature Publishing Group UK 2020-05-20 /pmc/articles/PMC7239898/ /pubmed/32433581 http://dx.doi.org/10.1038/s41598-020-65338-w Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Song, Lei
Zhang, Jian-gang
Zheng, Long
Feng, Xu
Hou, Jie
Zhang, Huan-ling
Liu, Shu-feng
Establishment of rat liver cancer cell lines with different metastatic potential
title Establishment of rat liver cancer cell lines with different metastatic potential
title_full Establishment of rat liver cancer cell lines with different metastatic potential
title_fullStr Establishment of rat liver cancer cell lines with different metastatic potential
title_full_unstemmed Establishment of rat liver cancer cell lines with different metastatic potential
title_short Establishment of rat liver cancer cell lines with different metastatic potential
title_sort establishment of rat liver cancer cell lines with different metastatic potential
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7239898/
https://www.ncbi.nlm.nih.gov/pubmed/32433581
http://dx.doi.org/10.1038/s41598-020-65338-w
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