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Ecto-5′-nucleotidase (CD73) is a biomarker for clear cell renal carcinoma stem-like cells
Identification of a specific biomarker for cancer stem cells (CSCs) is of potential applications in the development of effective therapeutic strategies for renal cell carcinoma (RCC). In this study, both the RCC cell line 786-O and surgically removed clear cell RCC (ccRCC) tissues were implemented t...
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/PMC5458263/ https://www.ncbi.nlm.nih.gov/pubmed/28404888 http://dx.doi.org/10.18632/oncotarget.16667 |
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author | Song, Lei Ye, Wenling Cui, Yong Lu, Jianzhong Zhang, Yanan Ding, Nan Hu, Wentao Pei, Hailong Yue, Zhongjin Zhou, Guangming |
author_facet | Song, Lei Ye, Wenling Cui, Yong Lu, Jianzhong Zhang, Yanan Ding, Nan Hu, Wentao Pei, Hailong Yue, Zhongjin Zhou, Guangming |
author_sort | Song, Lei |
collection | PubMed |
description | Identification of a specific biomarker for cancer stem cells (CSCs) is of potential applications in the development of effective therapeutic strategies for renal cell carcinoma (RCC). In this study, both the RCC cell line 786-O and surgically removed clear cell RCC (ccRCC) tissues were implemented to grew as spheroids in serum-free medium supplemented with mitogens. This subpopulation possessed key characteristics defining CSCs. We also identified that surgically removed ccRCC tissues were heterogenic and there was a subpopulation of cells that was highly stained with rhodamine-123. Based on membrane-proteomic analyses, CD73 was identified as a candidate biomarker. We further found that CD73(high) cells were highly tumorigenic. As few as 100 CD73(high) cells were capable of forming xenograft tumors in non obese diabetic/severe combined immunodeficiency disease mice, whereas 1 × 10(5) CD73(low) cells did not initiate tumor formation. During successive culture, the CD73(high) population regenerated both CD73(high) and CD73(low) cells, whereas the CD73(low) population remained low expression level of CD73. Furthermore, the CD73(high) cells were more resistant to radiation and DNA-damaging agents than the CD73(low) cells, and expressed a panel of ‘stemness’ genes at a higher level than the CD73(low) cells. These findings suggest that a high level of CD73 expression is a bona fide biomarker of ccRCC stem-like cells. Future research will aim at the elucidation of the underlying mechanisms of CD73 in RCC development and the distinct aspects of ccRCC stem-like cells from other tumor types. |
format | Online Article Text |
id | pubmed-5458263 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-54582632017-06-08 Ecto-5′-nucleotidase (CD73) is a biomarker for clear cell renal carcinoma stem-like cells Song, Lei Ye, Wenling Cui, Yong Lu, Jianzhong Zhang, Yanan Ding, Nan Hu, Wentao Pei, Hailong Yue, Zhongjin Zhou, Guangming Oncotarget Research Paper Identification of a specific biomarker for cancer stem cells (CSCs) is of potential applications in the development of effective therapeutic strategies for renal cell carcinoma (RCC). In this study, both the RCC cell line 786-O and surgically removed clear cell RCC (ccRCC) tissues were implemented to grew as spheroids in serum-free medium supplemented with mitogens. This subpopulation possessed key characteristics defining CSCs. We also identified that surgically removed ccRCC tissues were heterogenic and there was a subpopulation of cells that was highly stained with rhodamine-123. Based on membrane-proteomic analyses, CD73 was identified as a candidate biomarker. We further found that CD73(high) cells were highly tumorigenic. As few as 100 CD73(high) cells were capable of forming xenograft tumors in non obese diabetic/severe combined immunodeficiency disease mice, whereas 1 × 10(5) CD73(low) cells did not initiate tumor formation. During successive culture, the CD73(high) population regenerated both CD73(high) and CD73(low) cells, whereas the CD73(low) population remained low expression level of CD73. Furthermore, the CD73(high) cells were more resistant to radiation and DNA-damaging agents than the CD73(low) cells, and expressed a panel of ‘stemness’ genes at a higher level than the CD73(low) cells. These findings suggest that a high level of CD73 expression is a bona fide biomarker of ccRCC stem-like cells. Future research will aim at the elucidation of the underlying mechanisms of CD73 in RCC development and the distinct aspects of ccRCC stem-like cells from other tumor types. Impact Journals LLC 2017-03-29 /pmc/articles/PMC5458263/ /pubmed/28404888 http://dx.doi.org/10.18632/oncotarget.16667 Text en Copyright: © 2017 Song 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 (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Song, Lei Ye, Wenling Cui, Yong Lu, Jianzhong Zhang, Yanan Ding, Nan Hu, Wentao Pei, Hailong Yue, Zhongjin Zhou, Guangming Ecto-5′-nucleotidase (CD73) is a biomarker for clear cell renal carcinoma stem-like cells |
title | Ecto-5′-nucleotidase (CD73) is a biomarker for clear cell renal carcinoma stem-like cells |
title_full | Ecto-5′-nucleotidase (CD73) is a biomarker for clear cell renal carcinoma stem-like cells |
title_fullStr | Ecto-5′-nucleotidase (CD73) is a biomarker for clear cell renal carcinoma stem-like cells |
title_full_unstemmed | Ecto-5′-nucleotidase (CD73) is a biomarker for clear cell renal carcinoma stem-like cells |
title_short | Ecto-5′-nucleotidase (CD73) is a biomarker for clear cell renal carcinoma stem-like cells |
title_sort | ecto-5′-nucleotidase (cd73) is a biomarker for clear cell renal carcinoma stem-like cells |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5458263/ https://www.ncbi.nlm.nih.gov/pubmed/28404888 http://dx.doi.org/10.18632/oncotarget.16667 |
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