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TRAIL-R1 as a novel surface marker for circulating giant cell tumor of bone
Giant cell tumor of bone (GCT), which frequently occurs in the patients’ spine, is relatively prevalent in Chinese population. A group of GCT invades into vessels and appears to be circulating tumor cells (CTCs) responsible for the distal metastasis of the primary tumor. So far the cell surface mark...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5584197/ https://www.ncbi.nlm.nih.gov/pubmed/28881598 http://dx.doi.org/10.18632/oncotarget.17042 |
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author | Liu, Jian-Xiang Zhang, Zhi-Cai Shao, Zeng-Wu Pu, Fei-Fei Wang, Bai-Chuan Zhang, Yu-Kun Zeng, Xian-Lin Guo, Xiao-Dong Yang, Shu-Hua He, Tong-Chuan |
author_facet | Liu, Jian-Xiang Zhang, Zhi-Cai Shao, Zeng-Wu Pu, Fei-Fei Wang, Bai-Chuan Zhang, Yu-Kun Zeng, Xian-Lin Guo, Xiao-Dong Yang, Shu-Hua He, Tong-Chuan |
author_sort | Liu, Jian-Xiang |
collection | PubMed |
description | Giant cell tumor of bone (GCT), which frequently occurs in the patients’ spine, is relatively prevalent in Chinese population. A group of GCT invades into vessels and appears to be circulating tumor cells (CTCs) responsible for the distal metastasis of the primary tumor. So far the cell surface markers of GCT have not been determined. In the current study, we aimed to identify a novel CTC marker with higher specificity in GCT. TRAIL-R1+ cells were purified from GCT cell lines. The TRAIL-R1+ cells were compared with total GCT cells for tumor sphere formation, chemo-resistance, tumor formation in nude mice, and frequency of developing distal metastases. We found that TRAIL-R1+ GCT cells appeared to be highly enriched for CTCs in GCT. Compared to total GCT cells, TRAIL-R1+ GCT cells generated significantly more tumor spheres in culture, were higher chemo-resistant, and had a higher frequency of being detected in the circulation after subcutaneous transplantation as well as development of distal metastases. Thus, we conclude that TRAIL-R1+ may be a novel CTC marker in GCT. Selective elimination of TRAIL-R1+ GCT cells may improve the current GCT therapy. |
format | Online Article Text |
id | pubmed-5584197 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-55841972017-09-06 TRAIL-R1 as a novel surface marker for circulating giant cell tumor of bone Liu, Jian-Xiang Zhang, Zhi-Cai Shao, Zeng-Wu Pu, Fei-Fei Wang, Bai-Chuan Zhang, Yu-Kun Zeng, Xian-Lin Guo, Xiao-Dong Yang, Shu-Hua He, Tong-Chuan Oncotarget Research Paper Giant cell tumor of bone (GCT), which frequently occurs in the patients’ spine, is relatively prevalent in Chinese population. A group of GCT invades into vessels and appears to be circulating tumor cells (CTCs) responsible for the distal metastasis of the primary tumor. So far the cell surface markers of GCT have not been determined. In the current study, we aimed to identify a novel CTC marker with higher specificity in GCT. TRAIL-R1+ cells were purified from GCT cell lines. The TRAIL-R1+ cells were compared with total GCT cells for tumor sphere formation, chemo-resistance, tumor formation in nude mice, and frequency of developing distal metastases. We found that TRAIL-R1+ GCT cells appeared to be highly enriched for CTCs in GCT. Compared to total GCT cells, TRAIL-R1+ GCT cells generated significantly more tumor spheres in culture, were higher chemo-resistant, and had a higher frequency of being detected in the circulation after subcutaneous transplantation as well as development of distal metastases. Thus, we conclude that TRAIL-R1+ may be a novel CTC marker in GCT. Selective elimination of TRAIL-R1+ GCT cells may improve the current GCT therapy. Impact Journals LLC 2017-04-11 /pmc/articles/PMC5584197/ /pubmed/28881598 http://dx.doi.org/10.18632/oncotarget.17042 Text en Copyright: © 2017 Liu et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Liu, Jian-Xiang Zhang, Zhi-Cai Shao, Zeng-Wu Pu, Fei-Fei Wang, Bai-Chuan Zhang, Yu-Kun Zeng, Xian-Lin Guo, Xiao-Dong Yang, Shu-Hua He, Tong-Chuan TRAIL-R1 as a novel surface marker for circulating giant cell tumor of bone |
title | TRAIL-R1 as a novel surface marker for circulating giant cell tumor of bone |
title_full | TRAIL-R1 as a novel surface marker for circulating giant cell tumor of bone |
title_fullStr | TRAIL-R1 as a novel surface marker for circulating giant cell tumor of bone |
title_full_unstemmed | TRAIL-R1 as a novel surface marker for circulating giant cell tumor of bone |
title_short | TRAIL-R1 as a novel surface marker for circulating giant cell tumor of bone |
title_sort | trail-r1 as a novel surface marker for circulating giant cell tumor of bone |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5584197/ https://www.ncbi.nlm.nih.gov/pubmed/28881598 http://dx.doi.org/10.18632/oncotarget.17042 |
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