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Clinical implications of cancer stem cell-like side population cells in human laryngeal cancer
In this study, we try to detect and isolate the cancer stem cell-like side population cells (SP) from the laryngeal carcinoma cell line and primary laryngeal carcinoma and explore the clinical implications of SP cells in laryngeal carcinoma. The SP cells and non-side population cells (NSP) cells wer...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3879800/ https://www.ncbi.nlm.nih.gov/pubmed/23807678 http://dx.doi.org/10.1007/s13277-013-0941-6 |
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author | Yu, Dan Jin, Chunshun Liu, Yan Yang, Jingpu Zhao, Yin Wang, Haitao Zhao, Xue Cheng, Jinzhang Liu, Xueshibojie Liu, Caigang |
author_facet | Yu, Dan Jin, Chunshun Liu, Yan Yang, Jingpu Zhao, Yin Wang, Haitao Zhao, Xue Cheng, Jinzhang Liu, Xueshibojie Liu, Caigang |
author_sort | Yu, Dan |
collection | PubMed |
description | In this study, we try to detect and isolate the cancer stem cell-like side population cells (SP) from the laryngeal carcinoma cell line and primary laryngeal carcinoma and explore the clinical implications of SP cells in laryngeal carcinoma. The SP cells and non-side population cells (NSP) cells were sorted by Hoechst 33342 through FACS. The proliferation capacity, invasion ability, migration ability, and tumorigenic activity of the SP cells were evaluated. In addition, the association between the SP cells ratio and the prognostic factors of laryngeal cancer was analyzed. As a result, the percentage of the SP cells in Hep-2 cells was 5.1 %. The SP cells depicted float colonies, but the NSP cells failed to generate the typical cell spheres. The clone formation ratios were 47.47 ± 10.20 % vs. 4.98 ± 1.41 % in the flat plates and 46.82 ± 5.67 % vs. 12.53 ± 3.51 % in the soft agar for SP and NSP cells (P = 0.01 and 0.01). The SP cells depicted a higher migrating potency than the NSP cells in both the transwell assay and scarification test (all P < 0.05). The matrigel invasion assay showed that the artificial basement membrane penetration rate of SP cells was 39.04 ± 4.78 %, which was higher than 25.16 ± 4.63 % of the NSP cells (P < 0.05). Only 10(3) SP cells were able to form tumors in mice, whereas 10(4) NSP cells failed to form tumors. The SP cells were correlated with the differentiation, lymph node metastasis, and clinical stage of the laryngeal cancers. In conclusion, SP cells may be a potential prognostic factor of laryngeal cancer. |
format | Online Article Text |
id | pubmed-3879800 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-38798002014-01-06 Clinical implications of cancer stem cell-like side population cells in human laryngeal cancer Yu, Dan Jin, Chunshun Liu, Yan Yang, Jingpu Zhao, Yin Wang, Haitao Zhao, Xue Cheng, Jinzhang Liu, Xueshibojie Liu, Caigang Tumour Biol Research Article In this study, we try to detect and isolate the cancer stem cell-like side population cells (SP) from the laryngeal carcinoma cell line and primary laryngeal carcinoma and explore the clinical implications of SP cells in laryngeal carcinoma. The SP cells and non-side population cells (NSP) cells were sorted by Hoechst 33342 through FACS. The proliferation capacity, invasion ability, migration ability, and tumorigenic activity of the SP cells were evaluated. In addition, the association between the SP cells ratio and the prognostic factors of laryngeal cancer was analyzed. As a result, the percentage of the SP cells in Hep-2 cells was 5.1 %. The SP cells depicted float colonies, but the NSP cells failed to generate the typical cell spheres. The clone formation ratios were 47.47 ± 10.20 % vs. 4.98 ± 1.41 % in the flat plates and 46.82 ± 5.67 % vs. 12.53 ± 3.51 % in the soft agar for SP and NSP cells (P = 0.01 and 0.01). The SP cells depicted a higher migrating potency than the NSP cells in both the transwell assay and scarification test (all P < 0.05). The matrigel invasion assay showed that the artificial basement membrane penetration rate of SP cells was 39.04 ± 4.78 %, which was higher than 25.16 ± 4.63 % of the NSP cells (P < 0.05). Only 10(3) SP cells were able to form tumors in mice, whereas 10(4) NSP cells failed to form tumors. The SP cells were correlated with the differentiation, lymph node metastasis, and clinical stage of the laryngeal cancers. In conclusion, SP cells may be a potential prognostic factor of laryngeal cancer. Springer Netherlands 2013-06-27 /pmc/articles/PMC3879800/ /pubmed/23807678 http://dx.doi.org/10.1007/s13277-013-0941-6 Text en © The Author(s) 2013 https://creativecommons.org/licenses/by-nc/2.0/ Open Access This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Research Article Yu, Dan Jin, Chunshun Liu, Yan Yang, Jingpu Zhao, Yin Wang, Haitao Zhao, Xue Cheng, Jinzhang Liu, Xueshibojie Liu, Caigang Clinical implications of cancer stem cell-like side population cells in human laryngeal cancer |
title | Clinical implications of cancer stem cell-like side population cells in human laryngeal cancer |
title_full | Clinical implications of cancer stem cell-like side population cells in human laryngeal cancer |
title_fullStr | Clinical implications of cancer stem cell-like side population cells in human laryngeal cancer |
title_full_unstemmed | Clinical implications of cancer stem cell-like side population cells in human laryngeal cancer |
title_short | Clinical implications of cancer stem cell-like side population cells in human laryngeal cancer |
title_sort | clinical implications of cancer stem cell-like side population cells in human laryngeal cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3879800/ https://www.ncbi.nlm.nih.gov/pubmed/23807678 http://dx.doi.org/10.1007/s13277-013-0941-6 |
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